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Journal articles on the topic 'Deaf Mutism'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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1

Elamin, Abdelaziz. "Goitre and Deaf-Mutism." Upsala Journal of Medical Sciences 96, no. 3 (1991): 213–18. http://dx.doi.org/10.3109/03009739109179273.

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2

Maskey, Narbada Lal. "Deaf - Mutism A Clinical Analysis." Journal of Nepal Medical Association 3, no. 1 (2003): 1–7. http://dx.doi.org/10.31729/jnma.901.

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3

LUNDBORG, H. "HEREDITARY TRANSMISSION OF GENOTYPICAL DEAF-MUTISM." Hereditas 1, no. 1 (2010): 35–40. http://dx.doi.org/10.1111/j.1601-5223.1920.tb02450.x.

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4

CSANÁDY, M., M. HÖGYE, and T. FORSTER. "Hypertrophic cardiomyopathy associated with congenital deaf-mutism." European Heart Journal 8, no. 5 (1987): 528–34. http://dx.doi.org/10.1093/oxfordjournals.eurheartj.a062313.

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5

BITTLES, A. H., S. G. SULLIVAN, and L. A. ZHIVOTOVSKY. "CONSANGUINITY, CASTE AND DEAF-MUTISM IN PUNJAB, 1921." Journal of Biosocial Science 36, no. 2 (2004): 221–34. http://dx.doi.org/10.1017/s0021932003006230.

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The effects of religion, population sub-division and geography on the prevalence of deaf-mutism were investigated using information collected in the 1921 Census of Punjab. The total sample size was 9·36 million, and comprised data on thirteen Hindu castes, seventeen Muslim biraderis and two Sikh castes. A two-way analysis of variance comparing males in Hindu castes in which consanguineous marriage was prohibited, with males in Muslim biraderis which favoured first cousin marriage, indicated major differences with respect to the patterns of deaf-mutism within each religion. In the Muslim popula

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6

Cozza, Andrea, Valerio Maria Di Pasquale Fiasca, and Alessandro Martini. "Congenital Deafness and Deaf-Mutism: A Historical Perspective." Children 11, no. 1 (2023): 51. http://dx.doi.org/10.3390/children11010051.

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Hearing loss is the most common sensory deficit and one of the most common congenital abnormalities. The estimated prevalence of moderate and severe hearing loss in a normal newborn is 0.1–0.3%, while the prevalence is 2–4% in newborns admitted to the newborn intensive care unit. Therefore, early detection and prompt treatment are of utmost importance in preventing the unwanted sequel of hearing loss on normal language development. The problem of congenital deafness is today addressed on the one hand with hearing screening at birth, on the other with the early (at around 3 months of age) appli

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7

Marriage, K., M. Govorchin, P. George, and C. Dilworth. "Use of an Amytal Interview in the Management of Factitious Deaf Mutism." Australian & New Zealand Journal of Psychiatry 22, no. 4 (1988): 454–56. http://dx.doi.org/10.3109/00048678809161356.

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We describe the case of a young woman presenting with deaf mutism and self-damaging behaviour. We emphasize the active investigation of psychological and physical symptoms, combined with gradual and gentle confrontation in a supportive setting.

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8

Karpouzis, Anthony, Alexandra Giatromanolaki, Efthimios Sivridis, et al. "Cutaneous Abrikossoff's tumour in coexistence with congenital deaf-mutism." European Journal of Dermatology 20, no. 3 (2010): 388–90. http://dx.doi.org/10.1684/ejd.2010.0902.

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9

Hu, D. N., W. Q. Qiu, B. T. Wu, et al. "Prevalence and genetic aspects of deaf mutism in Shanghai." Journal of Medical Genetics 24, no. 10 (1987): 589–92. http://dx.doi.org/10.1136/jmg.24.10.589.

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10

Nakagawa, M., Y. Kaminishi, Y. Isashiki, et al. "Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodvstrophy." Acta Neurologica Scandinavica 92, no. 1 (2009): 102–8. http://dx.doi.org/10.1111/j.1600-0404.1995.tb00475.x.

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11

Oshima, Takeshi, Takayuki Kudo, and Katsuhisa Ikeda. "Point Mutation of the Mitochondrial Genome in Japanese Deaf-Mutism." ORL 63, no. 6 (2001): 329–32. http://dx.doi.org/10.1159/000055769.

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12

PERIS, K., E. F. SALVATI, G. TORLONE, and S. CHIMENTI. "Keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with congenital deaf-mutism." British Journal of Dermatology 132, no. 4 (2006): 617–20. http://dx.doi.org/10.1111/j.1365-2133.1995.tb08721.x.

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13

songeunsung and Seungwon Hwang. "Interactive Sound Glove System for deaf mutism - Mainly with Kodaly Method -." Journal of Digital Design 12, no. 4 (2012): 397–404. http://dx.doi.org/10.17280/jdd.2012.12.4.037.

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14

SYLVESTER, P. E. "SPINO-CEREBELLAR DEGENERATION, HORMONAL DISORDER, HYPOGONADISM, DEAF MUTISM AND MENTAL DEFICIENCY." Journal of Intellectual Disability Research 16, no. 3 (2008): 203–14. http://dx.doi.org/10.1111/j.1365-2788.1972.tb01176.x.

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15

Aremu (FWACS), Shuaib K., Olushola A. Afolabi (FWACS), Biodun S. Alabi (FWACS), and Isiah O. Elemunkan (PhD. Speech therapist). "Epidemilogical Profile of Speech and Language Disorder in North Central Nigeria." International Journal of Biomedical Science 7, no. 4 (2011): 268–72. http://dx.doi.org/10.59566/ijbs.2011.7268.

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Background: Speech-language pathologists/Otolaryngologists recognize high prevalence of speech and language disorder among children. The aim of the study is to find out the epidemiological profile of speech and language disorder in north central Nigeria. Method: A five year retrospective review of all referral to speech and language therapy unit ENT Department between January 2005 and December 2009. Information retrieved and analysed included bio-data, clinical presentation and diagnosis of the patients.Descriptive analysis of these data were done. Results: A total of 146 patients were seen ou

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16

Holmgren, Stig. "CONGENITAL DEAF-MUTISM IN A FAMILY WITH DYSTROPHIA RETICULARIS LAMINAE PIGMENTOSAE RETINAE (SJÖGREN)." Acta Ophthalmologica 28, no. 3 (2009): 297–300. http://dx.doi.org/10.1111/j.1755-3768.1950.tb05362.x.

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17

Canpolat, Uğur, Cem Coteli, and Kudret Aytemir. "Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism." Indian Pacing and Electrophysiology Journal 17, no. 1 (2017): 16–17. http://dx.doi.org/10.1016/j.ipej.2017.01.002.

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18

Cline, Emily. "‘The bloody fingers … bear witness’: Sign Language and the Mute Detective in Susan Hopley and The Trail of the Serpent." Crime Fiction Studies 5, no. 1 (2024): 1–17. http://dx.doi.org/10.3366/cfs.2024.0107.

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In her examination of signing characters in works of Charles Dickens and Wilkie Collins, Jennifer Esmail highlights deaf characters’ absence in Victorian fiction. Mutism is more common, for example, in the character of Mary Elizabeth Braddon's working-class, fingerspelling Detective Peters (70, 10n24). Even so, sign language – seen as ‘primitive’ and ‘lacking [in] intellectual […] rigor’ – was rarely represented (Esmail 3). Dickens, Collins and Braddon, proto-detective novelists themselves, were preceded by Catherine Crowe, whose 1841 novel Susan Hopley features Julie le Moine, a female, cross

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19

Jervell, Anton, and Fred Lange Nielsen. "CONGENITAL DEAF-MUTISM, FUNCTIONAL HEART DISEASE WITH PROLONGATION OF THE Q-T INTERVAL, AND SUDDEN DEATH." Annals of Noninvasive Electrocardiology 4, no. 3 (1999): 362–71. http://dx.doi.org/10.1111/j.1542-474x.1999.tb00222.x.

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20

Arias, M. "A case of deaf-mutism as an expression of pure word deafness: neuroimaging and electrophysiological data." Neurocase 5, no. 5 (1999): 381a—381. http://dx.doi.org/10.1093/neucas/5.5.381-a.

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Arias, M., I. Requena, M. Ventura, I. Pereiro, A. Castro, and A. Alvarez. "A case of deaf-mutism as an expression of pure word deafness: neuroimaging and electrophysiological data." European Journal of Neurology 2, no. 6 (1995): 583–85. http://dx.doi.org/10.1111/j.1468-1331.1995.tb00179.x.

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22

Jain, Shraddha, and Sirjan Singh. "Factors associated with deaf-mutism in children attending special schools of rural central India: A survey." Journal of Family Medicine and Primary Care 9, no. 7 (2020): 3256. http://dx.doi.org/10.4103/jfmpc.jfmpc_222_20.

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23

Kaur, Harshindar, Sanjana Saholi, Pehal Goyal, and Kulwant Rai. "A Rare Case of Turner’s Syndrome with Deaf-mutism Reporting at Government Medical College, Patiala, Punjab, India." GMC PATIALA Journal of research and medical education 4, no. 2 (2021): 49–51. http://dx.doi.org/10.56412/gmcp.2021.4.2.89.

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24

Sen, Jayashree, Bitan Sen, Nikhil Akoijam Singh, Nitin Rajendra Alaspurkar, and Soumya Matturu. "Anesthetic Management in Pediatric Cochlear Implant." Journal of Datta Meghe Institute of Medical Sciences University 18, no. 3 (2023): 493–96. http://dx.doi.org/10.4103/jdmimsu.jdmimsu_517_22.

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Hearing loss can be conductive or sensorineural in nature. Sensorineural hearing loss (SNHL) affects the spiraling organ cochlea of the inner ear, which transforms the sound vibration into a neural signal or transmits it to the auditory part of the brain. Mild-to-severe SNHL, although can be rehabilitated successfully using hearing aids in extreme SNHL, hearing aids merely make the sound louder, distorted, and amplified where the clarity may be not enough for proper understanding to develop speech. Hence, in such cases, the best option for hearing and learning proper speech is a Cochlear impla

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25

HIGA, Tsutomu, Hiroyoshi HIRATSUKA, Toshimoto TENGAN, Etsuki SHINNO, and Hajime SUNAKAWA. "Perplexing perioperative management and surgical correction of jaw deformity in a patient with deaf-mutism and multiple missing teeth." Japanese Journal of Oral & Maxillofacial Surgery 48, no. 1 (2002): 35–38. http://dx.doi.org/10.5794/jjoms.48.35.

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26

Nguyen, Hao Trong, Nguyen Nhat Pham, Anh Vu Hoang, and Tu Nguyen Anh Tran. "The First Vietnamese Patient of LEOPARD Syndrome due to a PTPN11 Mutation: A Case Report and Review of the Literature." Case Reports in Genetics 2021 (September 11, 2021): 1–5. http://dx.doi.org/10.1155/2021/8197435.

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LEOPARD syndrome is a rare congenital anomaly that involves several organs. Patients with this syndrome develop multiple lentigines resembling a leopard’s hide. LEOPARD is an acronym of the major features constituting the syndrome including lentigines, electrocardiographic conduction defects, ocular hypertelorism, pulmonary valve stenosis, anomalies of genitalia, retardation of growth, and deafness. The syndrome is rare, and only 200 cases have been reported yet worldwide. We present the case of an 8-year-old female patient who visited the Ho Chi Minh City Hospital of Dermato-Venereology becau

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27

Richard, Gabriela, Thomas W. White, Lisa E. Smith, et al. "Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma." Human Genetics 103, no. 4 (1998): 393–99. http://dx.doi.org/10.1007/s004390050839.

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28

Masholeh, Ahmad Tibyanul, and Tri Erniawati. "Gangguan Mutisme Selektif Anak di Taman Kanak-kanak." Jurnal PAUD: Kajian Teori dan Praktik Pendidikan Anak Usia Dini 2, no. 2 (2019): 80. http://dx.doi.org/10.17977/um053v2i2p80-87.

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Abstract: The purpose of this study is (1) to describe the general picture of Selective Mutism disorders in research subjects, (2) to describe the factors causing the subject to experience Selective Mutism disorders, (3) to describe the efforts made by teachers and parents to deal with subjects with Selective Mutism disorders. . This study uses a qualitative description. The analysis used in this study came from the interactive model of analysis by Hubberman and Milles. Data collection is done by observation, interview and documentation techniques. Based on the results of the study it was foun

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29

Wagner, Josefine. "“Weakness of the Soul:” The Special Education Tradition at the Intersection of Eugenic Discourses, Race Hygiene and Education Policies." Conatus 4, no. 2 (2019): 83. http://dx.doi.org/10.12681/cjp.21073.

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According to Vera Moser, the first professorship of healing pedagogy, Heilpädagogik at the University of Zürich in 1931, established pedagogy of the disabled as an academic discipline. Through the definition of the smallest common denominator for all disabilities, which Heinrich Hanselmann called “weakness of the soul,” a connecting element of “imbecility, deaf-mutism, blindness, neglect and idiocy” was established. Under Nazi rule, school pedagogy advanced to völkisch, nationalist special pedagogy, shifting from the category of “innate imbecility” to a broader concept of disability. As an out

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30

Patel, Vishwal I., Darshna Dhedhi, Komal Pandya, Gaurav Sharma, and Richa Patel. "A retrospective study of the effect of dexmedetomidine infusion in cochlear implant surgery among pediatric patients." Indian Journal of Clinical Anaesthesia 9, no. 1 (2022): 71–74. http://dx.doi.org/10.18231/j.ijca.2022.015.

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Cochlear implantation surgery is usually performed in paediatric patient of 1 to 7 years of age with congenital deaf-mutism. Good results in this surgery are obtained by providing bloodless surgical field with controlled hypotension and postoperative smooth outcome. To anaesthetize these patients, we are using Inj Propofol, Inj fentanyl, Sevoflurane, Dexmedetomidine infusion and muscle relaxants. Dexmedetomidine is an active isomer of medetomidine and an agonist at α2 –adreno receptors. Medetomidine provides perioperative sedation and analgesia thus decreasing other general anaesthetic drug re

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31

Tripathy, Smritiratan. "Prevalence of goiter among school children and iodine content in edible salt and drinking water in Rampurhat Sub-division of Birbhum District in West Bengal, India." INDIAN JOURNAL OF PHYSIOLOGY AND ALLIED SCIENCES 76, no. 02 (2024): 35–38. https://doi.org/10.55184/ijpas.v76i02.258.

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Background: A deficiency of iodine in the diet leads to many visible and invisible health consequences. The major consequences of iodine deficiency are enlargement of the thyroid gland, mental defects, deaf mutism, stillbirth, and miscarriage. This study was conducted to determine the prevalence of goiter among schoolchildren in the Rampurhat Sub-division of Birbhum district in West Bengal. Methods: A total of 2712 school children (6–12 years) were clinically examined for goiter from eight CD Blocks and two Municipalities of the studied region. Iodine content in 350 salt samples and 80 drinkin

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32

Rapin, I. "A comment on “A case of deaf-mutism as an expression of pure word deafness: neuroimaging and electrophysiological data” by Arias et al.; TO THE EDITOR." European Journal of Neurology 3, no. 6 (1996): 605–6. http://dx.doi.org/10.1111/j.1468-1331.1996.tb00281.x.

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33

Denes, G. "A comment on “A case of deaf-mutism as an expression of pure word deafness: neuroimaging and electrophysiological data” by Arias et al.; TO THE EDITOR." European Journal of Neurology 3, no. 6 (1996): 607–8. http://dx.doi.org/10.1111/j.1468-1331.1996.tb00283.x.

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34

Melse-Boonstra, Alida, and Ian Mackenzie. "Iodine deficiency, thyroid function and hearing deficit: a review." Nutrition Research Reviews 26, no. 2 (2013): 110–17. http://dx.doi.org/10.1017/s0954422413000061.

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Iodine deficiency affects an estimated 241 million school-aged children in the world. Little is known about iodine deficiency in relation to auditory function, except for the fact that deaf–mutism is one of the features of cretinism. In the present review, we documented the scientific knowledge on the role of iodine and hypothyroidism in the auditory system. We found that ear development and hearing function depend on thyroid hormones. Multiple pathways are involved in this, including both inner ear morphology as well as neurological processes. Conductive as well as sensorineural hearing loss

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35

Dr., Kotnis Shubhalaxmi Devdatt. "Study of Prevalence of Iodine Deficiency Disorders and Salt Consumption Patterns in an Urban area of South- West Maharashtra. A Cross Sectional Study." International Journal of Medical and Pharmaceutical Research 4, no. 2 (2023): 105–12. https://doi.org/10.5281/zenodo.7748373.

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<strong>Introduction</strong>: Globally more than 1•9 billion individuals have inadequate iodine nutrition of whom 285 million are school-aged children. [1] Nutritional Iodine deficiency could result in abortion, stillbirth, mental retardation, deaf mutism, squint, dwarfism, goitre, neuromotor defects etc. [2] Prevalence surveys of iodine status, including measurement of urinary iodine levels and an analysis of the salt situation is needed for sustained elimination. [3] It was found in India, 337 districts were endemic for Iodine deficiency disorder i.e., prevalence is >10% [4]. Commun

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36

Anwar, Khurshid, Shehryar Khan, Muhammad Afaq Ali, Mohammad Javaid, Muhammad Ismail Khan, and Isteraj Shahabi. "SEX & AGE-WISE DISTRIBUTION AND CAUSES OF DYSPHONIA IN CHILDREN." Gomal Journal of Medical Sciences 16, no. 3 (2018): 83–87. http://dx.doi.org/10.46903/gjms/16.03.1930.

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Background: Dysphonia is common in children due to which they suffer adversely both at home and at school. The objectives of this study were to determine the sex & age-wise distribution and causes of dysphonia in children. Materials & Methods: This descriptive cross-sectional study was conducted at the Department of ENT and Head & Neck surgery, Hayatabad Medical Complex, Peshawar, Pakistan from January 1, 2017 to December 31, 2018. Sample size consisted of 72 patients presenting with chronic dysphonia, selected using the non-probability consecutive sampling technique Inclusion crit

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37

Rifqi, Kafin, and Dicky Hermawan. "Neglected Congenital Rubella Syndrome in 10-Year-Old Boy." Vision Science and Eye Health Journal 1, no. 2 (2022): 54–57. http://dx.doi.org/10.20473/vsehj.v1i2.2022.54-57.

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Introduction: Cataract, congenital heart defect, and hearing impairment are the three most common manifestations of congenital rubella syndrome (CRS) that lead to developmental delay in the children. CRS usually present during the infant period of three months old as the median age number. Ironically, we found a 10-year-old boy who was diagnosed with CRS and there was no significant plan to improve his condition anymore because of his neglected by family. The purpose of this case report is to alert primary health workers and also ophthalmologists to do our best to prevent blindness due to cata

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38

Fando, Roman. "Russian women at the beginning of human genetics." History of science and technology 10, no. 1(16) (2020): 110–26. http://dx.doi.org/10.32703/2415-7422-2020-10-1(16)-110-126.

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This paper reviews the studies on human genetics, carried out by Russian women in the 1920s and 1930s. Its main objective is to determine the contribution of women scientists to the development of different fields of human genetics. Particular attention is given to reconstructing women geneticists’ research work, reviewing the content of their publications, and analysing the theoretical and methodological approaches they employed to tackle different scientific problems. The biographies of the pioneers in Russian “anthropogenetics” (knowledge of human heredity), R. I. Serebrovskaya, G. V. Sobol

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39

Cahyadini, Amelia, Abi Ma’ruf Radjab, and Chyntia Pinky. "MUTASI: BENTUK SANKSI DI BIDANG KEPEGAWAIAN?" Veritas et Justitia 6, no. 1 (2020): 49–67. http://dx.doi.org/10.25123/vej.3425.

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In the civil servant management system, developed on the basis of merit system, any official can be at any time be transferred, promoted or demoted. In practice this option may and have often been misused as tool in office politics to remove troublesome civil servant. From the civil servant’s perspective, the options open are either comply or decline the standing order and face the consequence of disciplinary sanction. This article shall discuss, using a legal/juridical normative method, legal aspects of this management tool. The aim is to propose a guidance for civil servants on how to deal w

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40

Cavalcante, Isabella Ayres Alfonso, Maria Clara Machado Breves, Sheila Rejane Niskier, Barbara Soares da Silva, Clara Maria Rocha Cipriano, and Maria Sylvia de Souza Vitalle. "Problematic use of TikTok and mutism in an adolescent with Down syndrome: Case report and Literature Review." International Journal of Multidisciplinary Research and Growth Evaluation 5, no. 5 (2024): 722–25. http://dx.doi.org/10.54660/.ijmrge.2024.5.5.722-725.

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Problematic use of social media by adolescents, including TikTok, generates several negative consequences in the short and in the long term. This article reports the case of an adolescent who makes excessive and problematic use of social media, especially TikTok, and the development of aggressive behavior, mutism silence, and tics-like movements. During adolescence, social media is important for the development of cognitive and socio-emotional skills. However, problematic use has negative repercussions in several areas, including a higher incidence of depression, anxiety, impulsivity, psycholo

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Fredy, H. Martínez S., Robayo Betancourt Faiber, and Arbulú Mario. "A gesture recognition system for the Colombian sign language based on convolutional neural networks." Bulletin of Electrical Engineering and Informatics 9, no. 5 (2020): 2082–89. https://doi.org/10.11591/eei.v9i5.2440.

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Sign languages (or signed languages) are languages that use visual techniques, primarily with the hands, to transmit information and enable communication with deaf-mutes people. This language is traditionally only learned by people with this limitation, which is why communication between deaf and non-deaf people is difficult. To solve this problem we propose an autonomous model based on convolutional networks to translate the Colombian Sign Language (CSL) into normal Spanish text. The scheme uses characteristic images of each static sign of the language within a base of 24000 images (1000 imag

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42

Badrujaman, Adang. "Development of Android-Based Speech Recognition Application Using Learning Vector Quantization Method in Optimizing Deaf Communication." IJEEIT : International Journal of Electrical Engineering and Information Technology 5, no. 2 (2022): 41–49. http://dx.doi.org/10.29138/ijeeit.v5i2.1889.

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Tunarungu merupakan keadaan seseorang yang memiliki kelainan pada fungsi pendengarannya. Kondisi ini bisa berlangsung hanya sementara maupun permanen. Ada dua jenis gangguan pendengaran yang membuat seseorang menjadi penyandang tunarungu, pertama tunarungu yang bersifat bawaan (sudah ada sejak lahir), kedua tunarungu yang terjadi setelah dilahirkan. Tunarungu yang bersifat bawaan kemungkinan besar disebabkan oleh suatu mutasi genetik, keturunan dari orang tua, maupun terpapar penyakit ketika masih di dalam kandungan. Sedangkan tunarungu yang sifatnya terjadi setelah lahir biasanya disebabkan o

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43

Hund, Hilda-K., Brigitte Keller, and Franz Lingens. "Phenylalanine and Tyrosine Biosynthesis in Sporeforming Members of the Order Actinomycetales." Zeitschrift für Naturforschung C 42, no. 4 (1987): 387–93. http://dx.doi.org/10.1515/znc-1987-0410.

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Abstract The enzymes of the terminal steps of phenylalanine and tyrosine biosynthesis, chorismate mutase, prephenate dehydratase, arogenate dehydratase, prephenate dehydrogenase and aroge nate dehydrogenase were studied in 13 sporeforming members of the order Actinomycetales. In these organisms tyrosine is synthesized exclusively via arogenate, phenylalanine, however, via phenylpyruvate. The regulation pattern of the corresponding enzymes was determined: No feed back inhibition of arogenate dehydrogenase by L-phenylalanine and ʟ-tyrosine was observed. Chorismate mutase was found to be inhibi

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44

Jemimah, S., and S. R. Bheeter. "Removal of Procion Blue by Using Marsilea mutica Dead Biomass: Adsorption Kinetics and Equilibrium Studies." Asian Journal of Chemistry 29, no. 6 (2017): 1258–64. http://dx.doi.org/10.14233/ajchem.2017.20450.

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45

Xu, Sheng, Rungtiwa Phookamsak, Hong-Bo Jiang, et al. "First Report of Occultibambusa jonesii on Para Grass (Brachiaria mutica) in Yunnan, China." Chiang Mai Journal of Science 49, no. 3 (2022): 581–97. http://dx.doi.org/10.12982/cmjs.2022.048.

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During a survey of ascomycetes in Yunnan in the dry season (April 2021), an ascomycete was found on para grass [Brachiaria mutica (Forssk.) Stapf] submerged in a freshwater stream in Mengla County, Xishuangbanna Dai Autonomous Prefecture, Yunnan Province, China. Multi-locus phylogenetic analyses of combined ITS, LSU, SSU, tef1-α and rpb2 gene regions demonstrated that the novel strain (KUMCC 21-0469) shared the same branch length with Occultibambusa jonesii [GZCC 16-0117, ex-type strain] (98% ML, 1.00 PP) and grouped with O. aquatica with signifi cant support (91% ML, 1.00 PP). Morphological c

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46

Wu, Na, Asha J. Dissanayake, Hong-Zhi Du, and Jian-Kui Liu. "Morpho-Phylogenetic Evidence Reveals Novel Species and New Records of Botryosphaeriaceae in China and Thailand." Journal of Fungi 9, no. 11 (2023): 1051. http://dx.doi.org/10.3390/jof9111051.

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Species in the Botryosphaeriaceae are common plant pathogens, endophytes, and saprobes found on a variety of mainly woody hosts. Botryosphaeriaceae is a high-profile fungal family whose genera have been subjected to continuous revisions in recent years. Surveys conducted during 2019 and 2020 on several decaying woody hosts (from dead arial twigs, branches, stems, bark, and seed pods) in China and Thailand revealed a high diversity of Botryosphaeriaceae fungi. Identification of 16 Botryosphaeriaceae isolates was carried out based on both morphological characteristics and phylogenetic analyses o

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Moyo, P., L. Mostert, M. Bester, and F. Halleen. "Trunk Disease Fungi Associated With Diospyros kaki in South Africa." Plant Disease 100, no. 12 (2016): 2383–93. http://dx.doi.org/10.1094/pdis-02-16-0245-re.

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Persimmon trees with dieback symptoms and cankers were observed in three production areas in Western Cape Province in South Africa. Isolations were made from diseased branches, cankers, and pruning wounds as well as fungal fruiting bodies on dead branches and old pruning wounds. Several trunk disease pathogens were identified based on morphological characteristics and by molecular methods, including Diaporthe eres, D. infecunda, Eutypella citricola, E. microtheca, Phaeoacremonium parasiticum, P. scolyti, P. australiense, P. minimum, Fomitiporia capensis, Fomitiporia sp., Fomitiporella sp., and

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Kowalski, Tadeusz, and Agata Łukomska. "The studies on ash dying (Fraxinus excelsior L.) in the Włoszczowa Forest Unit stands." Acta Agrobotanica 58, no. 2 (2012): 429–40. http://dx.doi.org/10.5586/aa.2005.068.

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The studies were carried out in the Włoszczowa Forest Unit, in 9 ash stands differing in respect of age, origin (natural, artificial), site and in the nursery on 3 quarters differing due to a silvicultural method (transplanted and not transplanted) and seedlings age. In each stand an analysis of disease symptoms was carried out on 100 trees (2 - 20 years old stands) or 50 trees (21 - 80 years old stands) growing side by side in central part of the stand, while in the nursery in each block 200 seedlings were analyzed (4 sectors with 50 seedlings each). From the infected seedlings and trees 120

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Korza, George, Michelle Goulet, Angela DeMarco, James Wicander, and Peter Setlow. "Role of Bacillus subtilis Spore Core Water Content and pH in the Accumulation and Utilization of Spores’ Large 3-Phosphoglyceric Acid Depot, and the Crucial Role of This Depot in Generating ATP Early during Spore Germination." Microorganisms 11, no. 1 (2023): 195. http://dx.doi.org/10.3390/microorganisms11010195.

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The development of Bacillus spore cores involves the accumulation of 3-phosphoglycerate (3PGA) during sporulation, following core acidification to ~6.4, and before decreases in core water content occur due to Ca-dipicolinc acid (CaDPA) uptake. This core acidification inhibits phosphoglycerate mutase (PGM) at pH 6.4, allowing 3PGA accumulation, although PGM is active at pH 7.4. Spores’ 3PGA is stable for months at 4 °C and weeks at 37 °C. However, in wild-type spore germination, increases in core pH to 7.5–8 and in core water content upon CaDPA release and cortex peptidoglycan hydrolysis allow

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Reissig, Gabriela Niemeyer, Thiago Francisco de Carvalho Oliveira, Guilherme Cassão Marques Bragança, Rosane da Silva Rodrigues, and Frabrizio Da Fonseca Barbosa. "Fermented vegetables and fruits as vitamin B12 sources: An overview." International Food Research Journal 30, no. 5 (2023): 1093–104. http://dx.doi.org/10.47836/ifrj.30.5.02.

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There is a trend towards the consumption of plant foods, especially from the public that aims to reduce meat consumption. Plant-based food diets may have low source of vitamin B12 as plants do not produce them. A possible alternative to mitigate this is the consumption of fermented vegetables and fruits. Therefore, we aimed to provide an overview of the work being done with fermented vegetables and fruits, and show evidence that it is possible to obtain the necessary daily amount of vitamin B12 for human health and maintenance. Vitamin B12, also known as cobalamin, acts as a cofactor for the e

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