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1

Lee, Eun-Hye. "Convergence Characteristics of Contemporary Musical Vocal Techniques - Focusing on the Analysis of ‘The Girl in 14G’ -." Journal of the Korea Entertainment Industry Association 15, no. 4 (2021): 157–66. http://dx.doi.org/10.21184/jkeia.2021.6.15.4.157.

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2

Bakradze, Maiya D., Mariya I. Petrovskaiya, Dmitriy P. Polyakov, Anastasiya S. Polyakova, Anton A. Shavrov, and Vladimir K. Tatochenko. "Extensiv scleroma at 11 years old girl." Pediatrician (St. Petersburg) 7, no. 1 (2016): 135–41. http://dx.doi.org/10.17816/ped71135-141.

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Rhinoscleroma is a rare chronic granulomatous disease caused by Klebsiella rhinoscleromatis, which is a Gram-negative bacilli. Scleroma primarily affects the upper respiratory airway, preferably the nasal cavity, but the pharynx and larynx may also be involved. The term scleroma is preferred over the term rhinoscleroma because this disease affects not only the nose. Scleroma is endemic in countries of East Europe, Africa, South-East Asia and in sporadic areas worldwide. Scleroma usually begins at the nose and may progress to involve the larynx, pharynx or other regions of the neck. Scleroma ge
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de Boer, Anouk, Margot Peeters, and Ina Koning. "An Experimental Study of Risk Taking Behavior Among Adolescents: A Closer Look at Peer and Sex Influences." Journal of Early Adolescence 37, no. 8 (2016): 1125–41. http://dx.doi.org/10.1177/0272431616648453.

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In this experimental study, it was examined to what extent peers and sex were important predictors of risk taking behavior of adolescents. Participants were 140 Dutch adolescents (52.9% boys, 12-15 years) who completed the Balloon Analogue Risk Task (BART) as a measure of risk taking behavior, either individually or in the presence of homogenous or heterogeneous peer groups. Results showed that (a) adolescents took significantly more risk when they completed the BART with peers than when they completed the risk taking task individually, (b) boys took significantly more risk when they completed
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Mastroyianni, S., E. Kontopoulos, and K. Kanellopoulou. "140 Diastematomyelia in a girl with Angelman syndrome." European Journal of Paediatric Neurology 3, no. 6 (1999): A63. http://dx.doi.org/10.1016/s1090-3798(99)91153-4.

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5

Braman, George N. "The Girl in the National Gallery." Annals of Internal Medicine 144, no. 8 (2006): 595. http://dx.doi.org/10.7326/0003-4819-144-8-200604180-00010.

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6

Jain, K., BD Singh, A. Dubey, and A. Avinash. "Fibro-Epithelial Hyperplasia Mimicking Mucocele." Kathmandu University Medical Journal 12, no. 2 (2015): 146–48. http://dx.doi.org/10.3126/kumj.v12i2.13663.

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The effects of chronic local irritation have been seen commonly in the form of fibroma or mucocele in children. We report a ten year old girl with the chief complaint of swelling in the lower right region of labial mucosa which was diagnosed clinically as mucocele and histologically as fibro-epithelial hyperplasia. Surgical excision was done under local anesthesia with no post-operative complication.Kathmandu University Medical Journal Vol.12(2) 2014: 146-148
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Taran, Shachi Jain, Ravindra Kumar, and Manish Lodha. "Left Lung Agenesis with Bicuspid Aortic Valve." Journal of Nepal Paediatric Society 34, no. 2 (2014): 147–49. http://dx.doi.org/10.3126/jnps.v34i2.8792.

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Agenesis of the lung is an extremely rare congenital anomaly representing failure of development of the primitive lung bud. Here we are presenting a case of left lung agenesis with bicuspid aortic valve in a 17 year old girl who came with the complaints of backache only. The diagnosis was made on the basis of CECT and 2D Echocardiography. DOI: http://dx.doi.org/10.3126/jnps.v34i2.8792 J Nepal Paediatr Soc 2014;34(2):147-149
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Sarkar, Shatanik, Chaitali Patra, Chandrasekhar Dey, Malay Kumar Dasgupta, and Tapan Kumar Kundu. "Sturge Weber Syndrome Overlapping with Klippel Trenaunay Syndrome." Journal of Nepal Paediatric Society 33, no. 2 (2013): 147–49. http://dx.doi.org/10.3126/jnps.v33i2.7704.

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Sturge Weber syndrome (SWS) is a mesodermal phakomatosis characterized by meningo-facial angiomas with cerebral calcification. Klippel Trenaunay syndrome (KTS) is another very rare type of phakomatosis with cutaneous angiomas, varicose veins and enlargement of soft tissue or bones. Overlap between SWS & KTS is very rarely encountered. We report a three and half year old girl with overlapping features of both SWS and KTS. DOI: http://dx.doi.org/10.3126/jnps.v33i2.7704 J Nepal Paediatr Soc. 2013; 33(2):147-149
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Momen, Abdul Basit Ibne, Furial Quraishi Twinkle, Aminur Rahman, and Firoz Ahmed Quraishi. "Guillain-Barre Syndrome in a Case of Typhoid Fever: an Uncommon Association." Bangladesh Journal of Medicine 32, no. 2 (2021): 142–44. http://dx.doi.org/10.3329/bjm.v32i2.53799.

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Guillain-Barre syndrome (GBS) following typhoid is extremely uncommon and only few case reports are available in literature. The importance of this case report is to highlight upon the fact that a diagnosis of GBS should always be kept in mind whenever a patient of typhoid fever develops weakness. We report a young girl with blood culture proven typhoid fever that developed this very rare neurological complication quite early in the course of the disease. Following treatment with intravenous antibiotics and intravenous immunoglobulin, she was improved.
 Bangladesh J Medicine July 2021; 32
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10

Steuer, Faye B., Blair C. Bode, Kelley A. Rada, and James B. Hittner. "Gender Label and Perceived Infant Emotionality: A Partial Replication of a Classic Study." Psychological Reports 107, no. 1 (2010): 139–44. http://dx.doi.org/10.2466/07.10.17.pr0.107.4.139-144.

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In a study often referred to as “classic,” Condry and Condry (1976) showed a videotaped infant to participants, telling half of them the infant was a boy and half it was a girl. Participants who thought they were viewing a boy rated the infant's reaction to a jack-in-the-box as anger; those who thought they were viewing a girl rated the reaction as fear. Participants in the present partial replication of the Condrys' study did not rate the infant differently based on the infant's gender label, although there was evidence that participants' own sex affects their perception of an infant's emotio
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11

Armstrong, Neil, John Balding, Peter Gentle, Joanne Williams, and Brian Kirby. "Peak Oxygen Uptake and Physical Activity in 11- to 16-Year-Olds." Pediatric Exercise Science 2, no. 4 (1990): 349–58. http://dx.doi.org/10.1123/pes.2.4.349.

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The present study examined the relationship between peak V̇O2 and habitual physical activity in 11- to 16-year-old students. The peak V̇O2 of 111 girls and 85 boys was determined using treadmill or cycle ergometry. Habitual physical activity was estimated from minute-by-minute heart rate monitoring over three 12-hr periods during normal school days. Over half of the girls and one third of the boys failed to sustain a single 10-min period with their heart rate at or above 140 bpm. Only one boy sustained a daily 20-minute period with a heart rate at or above 160 bpm. During Saturday monitoring o
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12

Morozova, I. S., K. N. Belogai, and E. S. Kagan. "CHARACTERISTICS OF BODY IMAGE IN TEENAGE GIRLS ENGAGED IN FIGURE SKATING." Bulletin of Kemerovo State University, no. 1 (April 25, 2018): 147–52. http://dx.doi.org/10.21603/2078-8975-2018-1-147-152.

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The paper features the results of the study of the body image content characteristics in adolescent girls. The empirical study involved 12–14 year-old girls engaged in figure skating, and those not engaged in sports. The body image analysis was based on questionnaires and projective methods. It has been revealed that the content characteristics of the body image are interrelated with the parameters of self-relationship and self-esteem, regardless of whether the girl is engaged in sports or not. At the same time, athletes mostly appreciate the functional characteristics of the body, i.e. its ac
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13

Lingaraju, Naresh, PJ Nagarathna, R. Vijayalakshmi, and P. Sheshadri. "Osteogenesis Imperfecta/Lobstein Syndrome associated with Dentinogenesis Imperfecta." Journal of Contemporary Dental Practice 14, no. 1 (2013): 140–42. http://dx.doi.org/10.5005/jp-journals-10024-1288.

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ABSTRACT Osteogenesis imperfecta is a collagen related disorder characterized by increased bone fragility and low bone mass. The important oral finding in osteogenesis imperfect is the presence of dentinogenesis imperfecta. This article presents a case of osteogenesis imperfecta (type IV B) with dentinogenesis imperfecta where a 7-year-old girl had opalacent primary teeth associated with severe bone deformity, scoliosis, barrel shaped rib cage, and short stature. The clinical, radiographic ad histologic features are reviewed along with management aspects. How to cite this article Lingaraju N,
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14

Schutte, Anne Jacobson. "Irene di Spilimbergo: The Image of a Creative Woman in Late Renaissance Italy." Renaissance Quarterly 44, no. 1 (1991): 42–61. http://dx.doi.org/10.2307/2862405.

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What can you say about a twenty-five-year-old girl who died?" The classicist Erich Segal managed to wring 131 pages (and who knows how many millions of dollars) out of the short life of his fictional creation Jennifer Cavilleri, the heroine of Love Story. My subject is a real girl, the painter Irene di Spilimbergo, whose death at the age of twenty-one in 1559 evoked a tribute much more substantial, although probably not so lucrative for its editor, Dionigi Atanagi: a memorial volume containing 279 Italian and 102 Latin poems, a few anonymous but most written by 143 named contributors.
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15

Setz, J. M., A. A. A. van der Linde, G. P. J. M. Gerrits, and J. Meulstee. "EEG Findings in an Eleven-Year-Old Girl with Mercury Intoxication." Clinical EEG and Neuroscience 39, no. 4 (2008): 210–13. http://dx.doi.org/10.1177/155005940803900412.

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An 11-year-old female was seen at our outpatient clinic with a broad variety of symptoms that were due to elemental mercury intoxication. Electromyography and sequential electroencephalography findings obtained at days 2, 36, 88 and 148 are described. The patient was treated with chelation therapy during which she clinically improved considerably. A profound decrease in urinary mercury concentration occurred as well as normalization of the electroencephalogram.
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16

Chegodaeva, N. A., E. B. Olkhova, O. V. Zaytseva, et al. "Takayasu’s arteritis in a child with prolonged fever. Differential diagnosis. Clinical case analysis." Meditsinskiy sovet = Medical Council, no. 11 (August 12, 2021): 140–47. http://dx.doi.org/10.21518/2079-701x-2021-11-140-147.

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Takayasu’s arteritis is a chronic granulomatous arteritis with predominant involvement of the aorta and its main branches. It occurs both in youth and childhood, manifests between the ages of 10 and 30 years, female patients predominate. This article presents a clinical case of Takayasu’s arteritis in a child with prolonged fever. Clinical case. A 10-year-old girl E. was hospitalized with complaints of febrile fever episodes during the last two months; weakness and back pain were also noted. Observed by an endocrinologist since 2015 with a diagnosis of Stunted growth. Delayed physical develop
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17

Cioffi, Carmela. "SOME TEXTUAL PROBLEMS IN AELIUS DONATUS’ COMMENTARY ON TERENCE." Classical Quarterly 67, no. 1 (2017): 263–69. http://dx.doi.org/10.1017/s0009838817000039.

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In the first act of Terence's Andria, we find a dialogue between the old man Simo and Sosia, the freedman, with the former explaining why he has decided to arrange a false wedding for his young son Pamphilus. He has, in fact, learned that his son, despite being betrothed, has had a relationship with another girl and that—quite a serious matter—the fiancée's father, Chremes, has heard about the clandestine affair. In verses 144–9 Simo reports on the not-altogether friendly meeting he has had with Chremes, who is furious about the complete disrespect that has been shown to his daughter; Simo's o
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18

Kanik, Ali, Kayi Eliacik, Tolga Ince, Umit Bayol, and Mehmet Helvacı. "Cervical Lymphadenitis Due to Nodular Fasciitis in a Child." Journal of Nepal Paediatric Society 34, no. 2 (2014): 141–43. http://dx.doi.org/10.3126/jnps.v34i2.9548.

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Nodular fasciitis is a benign, reactive proliferation of fibroblasts in the subcutaneous tissues. It usually affects the trunk and upper extremities, and rarely the head and neck region of young adults. It is rare among children and the histologic findings may incorrectly suggest malignant lesions. We describe a two-year-old girl that referred to our clinic with complaints of fever and swelling on the right side of neck and diagnosed as lymphadenitis clinically. Cervical lymphadenitis due to nodular fasciitis is a rarity. We emphasize that nodular fasciitis needs to be included in the differen
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19

Lamb, John B. "The Wax Girl: Molding Little Nell in The Old Curiosity Shop." Dickens Studies Annual: Essays on Victorian Fiction 44, no. 1 (2013): 127–42. http://dx.doi.org/10.7756/dsa.044.007.127-142.

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20

Ouertani, Ines, Myriam Chaabouni, Ilhem Turki, et al. "A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia." European Journal of Medical Genetics 52, no. 4 (2009): 256–59. http://dx.doi.org/10.1016/j.ejmg.2009.01.004.

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21

Bhatta, Dharma Nand, AK Koirala, and N. Jha. "Adolescent students' attitude towards premarital sex and unwanted pregnancy." Health Renaissance 11, no. 2 (2013): 145–49. http://dx.doi.org/10.3126/hren.v11i2.8222.

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Background: In Nepal, as in other Asian countries, the issue on sexuality still remains a taboo. Despite this, there are increasing numbers of sexual activities reported among Nepalese adolescents. Objective: To know the attitude towards premarital sex and unwanted pregnancy of adolescent students. Methods: Three higher secondary schools were randomly selected and students of those schools were taken purposively with structured self administered questionnaires. Cross-sectional study design was adopted and significance levels were observed with 95% confidence level (pd.0.05 for significant). De
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22

Stamp, Shelley. "Lois Weber, Progressive Cinema, and the Fate of “The Work-a-Day Girl” in Shoes." Camera Obscura: Feminism, Culture, and Media Studies 19, no. 2 (2004): 141–69. http://dx.doi.org/10.1215/02705346-19-2_56-141.

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23

Sun, Feifei, Haiguang Tan, Yanshen Li, et al. "Metabolic Profile, Bioavailability and Toxicokinetics of Zearalenone-14-Glucoside in Rats after Oral and Intravenous Administration by Liquid Chromatography High-Resolution Mass Spectrometry and Tandem Mass Spectrometry." International Journal of Molecular Sciences 20, no. 21 (2019): 5473. http://dx.doi.org/10.3390/ijms20215473.

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Zearalenone-14-glucoside (ZEN-14G), a key modified mycotoxin, has attracted a great deal of attention due to the possible conversion to its free form of zearalenone (ZEN) exerting toxicity. In this study, the toxicokinetics of ZEN-14G were investigated in rats after oral and intravenous administration. The plasma concentrations of ZEN-14G and its major five metabolites were quantified using a validated liquid chromatography tandem mass spectrometry (LC-MS/MS) method. The data were analyzed via non-compartmental analysis using software WinNonlin 6.3. The results indicated that ZEN-14G was rapid
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24

Poort, Swibertus, Hans Vos, Rogier Bertina, et al. "Compound Heterozygosity for One Novel and One Recurrent Mutation in a Thai Patient with Severe Protein S Deficiency." Thrombosis and Haemostasis 81, no. 02 (1999): 189–92. http://dx.doi.org/10.1055/s-0037-1614440.

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SummaryHomozygous or compound heterozygous protein S (PS) deficiency is a very rare disorder in the anticoagulant system, that can lead to life-threatening thrombotic complications shortly after birth. This report describes the results of the genetic analysis of the PROS1 genes in a Thai girl patient. She was reported in 1990 as the first case with homozygous PS deficiency and neonatal purpura fulminans. In the present report, we identified the mutations in this patient by direct sequencing of PCR products representing all 15 exons of the PROS1 gene and their flanking intronic regions. The pat
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25

Vrotsos, Elena, Cristina Vincentelli, Amilcar Castellanos-Sanchez, and Gabriel Chamyan. "Angiocentric Glioma Presenting With Gait Ataxia and Right-Sided Angling of the Head in a 5-Year-Old Girl." American Journal of Clinical Pathology 140, suppl 1 (2013): A081. http://dx.doi.org/10.1093/ajcp/140.suppl1.081.

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26

Lepow, Gary M., Daniel L. Grimmer, Onya V. Lemar, and Evan A. Bridges. "Synovial Sarcoma in the Foot of a 5-Year-Old Child." Journal of the American Podiatric Medical Association 106, no. 4 (2016): 283–88. http://dx.doi.org/10.7547/12-141.

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The purpose of this case report is to present a rare finding of synovial sarcoma in a 5-year-old child. Most soft-tissue masses of the foot are too often presumed to be small and benign; therefore, compared with soft-tissue sarcomas, they are difficult to clinically differentiate and treat. A 5-year-old girl presented with a painful lesion that was diagnosed as synovial sarcoma after an excisional biopsy was performed. This was an unexpected finding of synovial sarcoma involving the tibialis posterior tendon of her right foot. The patient presented with an 8-month history of tenderness and an
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27

Islam, AHM Tohurul, Elora A. Leema, Tapos K. Das, O. Ibne Ali, MH Rahman, and Z. Nahar. "Hurler’s Syndrome - A Case Report (Mucopolysaccharidosis Type-1H)." TAJ: Journal of Teachers Association 24, no. 2 (2018): 148–51. http://dx.doi.org/10.3329/taj.v24i2.37546.

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A girl named Tania, aged 5yrs was brought to Shaheed Ziaur Rahman Medical College Hospital, Bogra with the complains of swelling of both legs for 5days & low grade intermittent fever for 1month & she also had severe mental retardation, facial dysmorphism, hepatosplenomegaly, umbilical hernia, corneal clouding, large calvaria & features of dysostosis multiplex. Her clinical as well as radiological features arouse strong suspicion suffering from a rare genetic disease (autosomal recessive) hurler’s syndrome though it wasn’t confirmed by deficiency of specific enzyme or urinary excret
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28

Muhammad Jamaluddin and Hajrah Hilal Ahmed. "Giant Ovarian Tumor Presenting as a Huge Abdomino-Pelvic Mass in a Teenage Girl: A Case Report." Journal of Bangladesh College of Physicians and Surgeons 39, no. 2 (2021): 137–41. http://dx.doi.org/10.3329/jbcps.v39i2.52394.

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Ovarian cysts are common causes of lower abdominal pain and abdominal distention in females. While most of them are benign and rarely grow immensely to achieve a huge size, they may be neoplastic in origin, reaching enormous dimensions with minimum or without raising any symptoms.Here, we present an interesting case of a 19-year-old female,who presented with huge abdominal swelling and pain in whole abdomen from whom a 9.1 kg borderline mucinous ovarian cyst, occupying the whole abdominal cavity was removed.
 J Bangladesh Coll Phys Surg 2021; 39(2): 137-141
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29

Beru Ginting, Sri Ulina. "SEMIOTIK MAKNA PADA WACANA NGEMBAH BELO SELAMBAR ADAT KARO LANGKAT (KAJIAN SEMIOTIKA SOSIAL)." Jurnal Pena Indonesia 3, no. 2 (2017): 130. http://dx.doi.org/10.26740/jpi.v3n2.p130-146.

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Ngembah Belo Selambar is one of the rituals of marriage of girls according to Karo custom. The purpose is to get the willingness of girl, parents, sembuyak, Anak Beru, Kalimbubu Singalo Bere-bere and kalimbubu Singalo perkempun on the proposal. Initially the event Ngembah Belo Selambar is done at night after finished eating. However, nowadays events are sometimes held at noon or afternoon, which begins or ends by eating together. Studying it through the social semiotics of the implementation of Ngembah Belo Selambar has a semiotic meaning of custom equipment used from Amak Mentar Kehamaten (Ho
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30

Amini, Razieh, Fatemeh Jahanshiri, Yasaman Amini, Zamberi Sekawi, and Farid Jalilian. "Detection of human coronavirus strain HKU1 in a 2 years old girl with asthma exacerbation caused by acute pharyngitis." Virology Journal 9, no. 1 (2012): 142. http://dx.doi.org/10.1186/1743-422x-9-142.

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31

Martins, Wilson Denis, Vania Portela Ditzel Westphalen, Fernando Henrique Westphalen, and Paulo Henrique Couto Souza. "Multiple Dentoalveolar Traumatic Lesions: Report of a Case and Proposition of Dental Polytrauma as a New Term." Journal of Contemporary Dental Practice 5, no. 4 (2004): 139–47. http://dx.doi.org/10.5005/jcdp-5-4-139.

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Abstract Traumatic injuries to permanent teeth are common, and dramatic episodes can occur during childhood. The aim of this paper is to present a report of severe trauma to the orofacial complex of an 8-year old girl that resulted in multiple injuries. The use of the term “dental polytrauma” (concomitant different dental traumatic injuries) is advocated in this case presentation. Citation Martins WD, Westphalen FH, Ditzel Westphalen VP, Souza PHC. Multiple Dentoalveolar Traumatic Lesions: Report of a Case and Proposition of Dental Polytrauma as a New Term. J Contemp Dent Pract 2004 November;(
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Sonati, Maria F., Beatriz I. Weinstein, Beatriz Erramouspe та ін. "HB Florida: A New Elongated C-Terminal β-Globin Variant Causing Dominant β-Thalassemia." Blood 104, № 11 (2004): 3776. http://dx.doi.org/10.1182/blood.v104.11.3776.3776.

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Abstract An elongated C-terminal β-globin variant, due to the deletion of one nucleotide (-C) in between codons 140/141 (GCC/CTG→GCC/TG), which modified the C-terminal sequence and added 10 more residues to the β-chain [(141)Trp-Pro-Thr-Ser-Ile-Thr-Lys-Leu-Ala-Phe-Leu-Leu-Ser-Asn-Phe-(156)Tyr-COOH], was found in an 8-year-old Argentine girl of Spanish descent with clinical picture of β-thalassemia intermedia. The patient presented chronic moderate hemolytic anemia (RBC=3.8x10¹²/L, Hb=8.6 g/dL, Hct=28%), with pallor, jaundice and liver and spleen enlargement, having required blood transfusion f
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Flanders, Michele M., Ronda A. Crist, William M. Roberts, and George M. Rodgers. "Pediatric Reference Intervals for Ten Coagulation Assays." Blood 104, no. 11 (2004): 2988. http://dx.doi.org/10.1182/blood.v104.11.2988.2988.

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Abstract There is a lack of reliable pediatric reference intervals for many clinical laboratory tests. In 2002, the Children’s Health Improvement through Laboratory Diagnostics (CHILDx) organization initiated a project to collect blood and urine samples from healthy children 7 – 17 years of age with the goal of establishing reference intervals for many laboratory tests. The purpose of the present study was to determine pediatric reference intervals for ten coagulation proteins associated with common bleeding and thrombotic disorders. All assays were functional except for vonWillebrand factor a
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34

Bryła, Marcin, Edyta Ksieniewicz-Woźniak, Agnieszka Waśkiewicz, et al. "Transformations of Selected Fusarium Toxins and Their Modified Forms During Malt Loaf Production." Toxins 12, no. 6 (2020): 385. http://dx.doi.org/10.3390/toxins12060385.

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An increasing number of studies have found that modified mycotoxins, such as free mycotoxins, naturally occur in food, and severely impact food safety. The present study investigated concentrations of trichothecenes nivalenol (NIV), deoxynivalenol (DON), and zearalenone (ZEN), together with their modified forms, nivalenol-3-glucoside (NIV-3G), deoxynivalenol-3-glucoside (DON-3G), and zearalenone-14-glucoside (ZEN-14G) and zearalenone-14-sulfate (ZEN-14S), respectively, at successive stages of malt loaf production (flour, dough kneading/fermentation, loaf baking). Toxins in bakery products orig
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35

Hendrata, Timothy, and Ribut Basuki. "PROJECT: SCREENPLAY FINDING ANDY." K@ta Kita 5, no. 1 (2017): 136–41. http://dx.doi.org/10.9744/katakita.5.1.136-141.

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This paper is about my screenplay entitled Finding Andy which I use as my final project. The screenplay itself is a story about a teenage girl who wants to improve her family’s poor communication. For my theory, I use John Gottman’s “The Four Horsemen of the Apocalypse Model” about family conflict. The theory helps me to shape my characters’ behavior towards each others. Since my characters has better relationship even though the brother dies in the end, I tend to use the worst level of family conflict in the beginning of the story and it gradually changes into successful communication which l
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Naderi, Majid, Akbar Dorgalaleh, Shaban Alizadeh, Shadi Tabibian, Bamedi Taregh, and Mehran Karimi. "The PAI-I Gene 4G/5G Polymorphism and Central Nervous System Bleeding In Factor XIII Deficiency." Blood 122, no. 21 (2013): 4782. http://dx.doi.org/10.1182/blood.v122.21.4782.4782.

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Background FXIII deficiency is one of the rare bleeding disorder (RBD) that has a highest incidence in Sistan and Baluchistan province around the world. This disorder represents with different clinical manifestations ranging from mild to severe bleeding tendency including CNS bleeding. The aim of this study is to evaluate the role of PAI-14G/5Gpolymorphism in central nervous bleeding (intra and extracranial hemorrhage) system in factor XIII deficiency. Methods In this case control study was studied 32 FXIII deficient patients with CNS bleeding and also 32 patients with factor XIII deficiency w
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Hollis, A. S. "Rights of Way in Ovid (Heroides 20.146) and Plautus (Curculio 36)." Classical Quarterly 44, no. 2 (1994): 545–49. http://dx.doi.org/10.1017/s0009838800044049.

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Acontius rhetorically addresses the young man to whom Cydippe's parents have betrothed her, whom he imagines as showing excessive familiarity while visiting the girl's sickbed. In line 146, ‘spes’ may be considered the vulgate reading; the noun can be used concretely, of the object of one's hopes (OLD 4), a person in whom hopes are centred (OLD 5), or sometimes as an endearment (OLD 5c). For application to a girl with suitors, cf. Ovid, Met. 4.795 ‘multorumque fuit spes invidiosa procorum’. Or one could take ‘spes’ in Her. 20.146 generally, = id quod spero. But, in any case, ‘spes’ is somewhat
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Ramazan, F. J. R. "Discourse of the Other in Agatha Christie’s An Autobiography." Literature and Culture of Polissya 98, no. 14f (2020): 142–53. http://dx.doi.org/10.31654/2520-6966-2020-14f-98-142-153.

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The paper discusses Jacques Lacan’s discourse of the other, relevant to the authority of societal influence and the creation of a person’s ego and alter egos. Inthis theory Lacan refers to the little others (i. e. the ego and alter egos) and the big Others (i. e. points of authority, societal expectations, and cultural norms). Studying one’s psychological makeup and development is a process that can be quite invasive and lengthy. However, there is a genre of literature that focuses directly on authors’ personal and introspective views of their own lives. Autobiographies are books in which auth
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Akbarzadeh, Marzieh, Tahereh Naderi, Mohammad H. Dabbaghmaneh, and Hamidreza Tabatabaee. "Comparison of Levels of Androgenic Hormones in various Phenotypes of Polycystic Ovarian Syndrome in High School Girls aging 14 to 18 Years." Journal of South Asian Federation of Obstetrics and Gynaecology 8, no. 1 (2016): 33–39. http://dx.doi.org/10.5005/jp-journals-10006-1382.

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ABSTRACT Introduction Polycystic ovarian syndrome (PCOS) is the most common endocrine disorder in women. Polycystic ovarian syndrome is mainly diagnosed based on oligomenorrhea or amenorrhea accompanied by clinical or laboratory evidence of hyperandrogenemia. This study aimed to compare the levels of androgenic hormones in various phenotypes of PCOS in high school girls aged 14 to 18 years in 2009. Materials and methods This cross-sectional study was conducted on 3200 girl students aged 14 to 18 years. The research community included high school girls in different educational districts of Shir
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O'Connor, Kathryn L., Melissa M. Baker, Sara L. Dalton, Thomas P. Dompier, Steven P. Broglio, and Zachary Y. Kerr. "Epidemiology of Sport-Related Concussions in High School Athletes: National Athletic Treatment, Injury and Outcomes Network (NATION), 2011–2012 Through 2013–2014." Journal of Athletic Training 52, no. 3 (2017): 175–85. http://dx.doi.org/10.4085/1062-6050-52.1.15.

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Context:Sports participation is one of the leading causes of concussions among nearly 8 million US high school student-athletes.Objective:To describe the epidemiology of sport-related concussion (SRC) in 27 high school sports during the 2011–2012 through 2013–2014 academic years.Design:Descriptive epidemiology study.Setting:Aggregate injury and exposure data from 27 sports in 147 high schools in the National Athletic Treatment, Injury and Outcomes Network (NATION).Patients or Other Participants:Boy and girl high school athletes during the 2011–2012 through 2013–2014 academic years.Main Outcome
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Yuwono, Natalia, Dominicus Husada, and Sukmawati Basuki. "PREVALENCE OF SOIL-TRANSMITTED HELMINTHIASIS AMONG ELEMENTARY CHILDREN IN SORONG DISTRICT, WEST PAPUA." Indonesian Journal of Tropical and Infectious Disease 7, no. 4 (2019): 86. http://dx.doi.org/10.20473/ijtid.v7i4.7362.

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Soil transmitted helminthiasis are common in the world and cause illness, especially in developing countries. It can cause infection in humans by contact with parasitic eggs or larvae that live in moist and warm soil. Soil-transmitted helminthiasis is often caused by Ascaris lumbricoides, Trichuris trichiura, Ancylostoma duodenale, and Necator americanus. In Indonesia, Soil transmitted helminthiasis prevalence is still high in some places. The tropical climate and high humidity support for the development of worms like in Sorong District, but there was no data. The purpose of this study is to
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Bliznakovska Stanchev, Dragica, Daniela Janjcevic, Dejan Trajkov, et al. "A case of a ten-year old girl with dominantly inherited Familial Mediterranean fever in Republic of Macedonia." Macedonian Pharmaceutical Bulletin 61, no. 2 (2015): 19–23. http://dx.doi.org/10.33320/maced.pharm.bull.2015.61.02.003.

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The Familial Mediterranean fever (FMF, MIM249100) is an autoimflammatory genetic disease characterized with recurrent painful attacks in the abdomen, chest or joints, usually accompanied with high body temperature. It is classically inherited in an autosomal recessive manner. It is associated with mutations of the MEFV gene, coding for the protein pyrin. More than 140 mutations of the MEFV gene are defined worldwide. Despite the progress in establishing reliable tests practical for routine use, as much as 20% of the patients with FMF remain without a detectable mutation in the MEFV gene. This
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Biederman, Joseph, Maura Fitzgerald, Thomas J. Spencer, et al. "Is Paternal Smoking at Conception a Risk for ADHD? A Controlled Study in Youth With and Without ADHD." Journal of Attention Disorders 24, no. 11 (2017): 1493–96. http://dx.doi.org/10.1177/1087054717690809.

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Objective: Based on emerging preclinical findings suggesting that paternal smoking at conception may be a risk for ADHD in the offspring, we investigated whether a similar effect can be observed in humans. Method: We analyzed data from an opportunistic dataset of girl probands with ( N = 140) and without ( N = 122) ADHD with available information on paternal smoking at conception. Data were analyzed using Pearson’s chi-square tests and multiple logistic regression. Results: ADHD probands had a significantly higher rate of paternal smoking at conception than controls (35% vs. 23%, χ2 = 3.82, p
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Husain, Shaikh Arshiya Kaiser, Anwaya R. Magare, Purushottam A. Giri, and Vijaykumar S. Jadhav. "Prevalence of somatic symptoms amongst undergraduate medical students of Marathwada region of Maharashtra, India." International Journal Of Community Medicine And Public Health 7, no. 12 (2020): 5106. http://dx.doi.org/10.18203/2394-6040.ijcmph20205192.

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Background: The aim of medical education is to produce competent, physically and mentally strong health professionals, as they are going to be the pillars of the future health care system. Stress is one of the most common and process-oriented obstacles in medical education. It often exerts a negative effect on the academic performance, physical health, and psychological well-being of the students. Dealing with overloaded medical curriculum, competing with peers, being away from home and meeting high expectations imposed by parents and society to excel is among the common stressful transitions
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Nataliya, Kitsera. "Congenital Anomalies of The Ear in Newborns from Lviv Region (west Ukraine) for 2006-2018 YY." Journal of Clinical Otorhinolaryngology 2, no. 1 (2020): 01–05. http://dx.doi.org/10.31579/jco/2020/006.

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Objectives The ear’s congenital anomalies usually occur in the outer, middle or inner ear separately or in combination. We had determined the сongenital ear’s anomalies (CEA) in newborns (2006-2018 yy) in West Ukraine, Lviv region. Methods 14 newborns who were diagnosed according to the reporting form by the maternity hospitals with CEA were analyzed over a period of 13 years.Results During the study period (2006–2018), there were 366 147 births reported, and 8634 newborns with birth defects, 14 were with CEA, an average incidence of 0.4 per 10 000 births. Our study included 10 boys and 4 girl
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Hoorntje, L. E., M. E. I. Schipper, A. Kaya, H. M. Verkooijen, J. G. Klinkenbijl, and I. H. M. Borel Rinkes. "Tumour cell displacement after 14G breast biopsy." European Journal of Surgical Oncology (EJSO) 30, no. 5 (2004): 520–25. http://dx.doi.org/10.1016/j.ejso.2004.03.001.

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Veršilovskis, A., J. Geys, B. Huybrechts, E. Goossens, S. De Saeger, and A. Callebaut. "Simultaneous determination of masked forms of deoxynivalenol and zearalenone after oral dosing in rats by LC-MS/MS." World Mycotoxin Journal 5, no. 3 (2012): 303–18. http://dx.doi.org/10.3920/wmj2012.1411.

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In vivo metabolism of masked or conjugated mycotoxins is poorly documented as standards are not commercially available and indirect analysis using hydrolytic enzymes is difficult to validate and cumbersome. We synthesised zearalenone-14-glucoside (ZEA-14G) chemically. Deoxynivalenol-3-glucuronide (DON-3GlcA) and glucuronides of 3- and 15-acetyl-deoxynivalenol (3- and 15-ADON-GlcAs), de-epoxydeoxynivalenol, zearalenone (ZEA), α- and β-zearalenol (α- and β-ZOL) were synthesised using rat microsomes. For the first time three ADON-GlcAs were synthesised: two 3-ADON-GlcAs and one 15-ADON-GlcA. Afte
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Rokeya, Ms, and A. K. Zunayet Ahammed. "A Shattering Epiphany in James Joyce’s “Araby”." Advances in Language and Literary Studies 8, no. 5 (2017): 140. http://dx.doi.org/10.7575/aiac.alls.v.8n.5p.140.

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This article attempts to show an adolescent boy's continuing process of self-realisation through his disillusionment with the bleak reality of Dublin in the early twentieth century in the short story “Araby” by James Joyce. Brought up in the drab and deadening surroundings with his uncle and aunt in conservative Catholic cultures, the lonely sensitive boy finds no outlets to express his feelings. Torn between harsh reality and imagination, the boy searches light and a relish of romance. Amidst the darkness, a girl, Mangan's sister, is the only light in his romantic vision. The boy, however, wi
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D’Amico, Mario, Pietro Sammarco, and Linda Pasta. "Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population." International Journal of Vascular Medicine 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/717480.

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Thrombophilic genetic factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A were studied as risk factors in 235 Caucasian subjects: 85 patients with abdominal thrombosis (54 with portal vein thrombosis (PVT) and 31 with Budd-Chiari syndrome (BCS) without liver cirrhosis or hepatocellular carcinoma) and 150 blood bank donors. Seventy-five patients with PVT/BCS showed associated disease or particular clinical status (46 PVT/29 BCS): 37 myeloproliferative neoplasm (20 PVT/17 BCS), 12 abdominal surgery (10 PVT/2 BCS), 10 contraception or pregnancy (6 PVT/4 BCS), 7 abdominal acute diseas
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im Walde, Th Schulte, J. C. Freundlich, Hermann Schwabedissen, and Wolfgang Taute. "Köln Radiocarbon Dates III." Radiocarbon 28, no. 1 (1986): 134–40. http://dx.doi.org/10.1017/s0033822200060045.

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The present list contains 14G dates from archaeologic samples attributed to the European Mesolithic period from the typology of associated finds, especially microliths. Of these samples, 14 are from Germany and 6 from France.
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