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Artículos de revistas sobre el tema "Clinical description"

Autor: Grafiati
Publicado: 9 de noviembre de 2024
Última modificación: 31 de julio de 2025

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1

Spiegel, David. "Clinical Description Introduction." American Journal of Psychiatry 151, no. 6 (1994): 90–96. http://dx.doi.org/10.1176/appi.ajp.151.6.90.

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2

CHIZH, ROMAN S., and ALBINA R. KHAKIMOVA. "LUMBOSACRAL PLEXOPATHY: CLINICAL CASE DESCRIPTION." Bulletin of Contemporary Clinical Medicine 11, no. 5 (2018): 143–48. http://dx.doi.org/10.20969/vskm.2018.11(5).143-148.

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Pachman, Lauren M. "Clinical description and epidemiology data." Clinical Immunology Newsletter 18, no. 10 (1998): 105–18. http://dx.doi.org/10.1016/s0197-1859(00)89058-5.

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4

Scharer, L. "Clinical Description of Nail Clubbing." JAMA: The Journal of the American Medical Association 286, no. 16 (2001): 1972–73. http://dx.doi.org/10.1001/jama.286.16.1972.

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5

Sitsko, N. V., G. S. Taub, G. V. Tsegelnik, et al. "WEGENER'S DISEASE: CLINICAL CASE DESCRIPTION." Journal of the Grodno State Medical University 23, no. 1 (2025): 60–64. https://doi.org/10.25298/2221-8785-2025-23-1-60-64.

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Wegener's disease is a systemic autoimmune disease associated with anti-neutrophil cytoplasmic antibodies, characterized by systemic granulomatous necrotizing vasculitis with the most common involvement of the upper and lower respiratory tract, kidneys, organs of vision and hearing and central nervous system. The onset of the disease, as a rule, manifests itself with nonspecific clinical symptoms, which complicates its diagnosis and delays specific treatment.
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6

Ohanyan, R. B., I. V. Roganova, D. Yu Konstantinov, and E. S. Kindalova. "Brain lymphoma: clinical case description." Bulletin of the Medical Institute "REAVIZ" (REHABILITATION, DOCTOR AND HEALTH) 14, no. 5 (2024): 101–7. https://doi.org/10.20340/vmi-rvz.2024.5.case.4.

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Relevance. Differential diagnosis between the brain infectious lesions and the central nervous system (СNS) oncological diseases is an urgent task in infectology.The aim of the study is to present and analyze a primary diffuse large-cell B-cell lymphoma of the central nervous system clinical case.Materials and methods. The work was carried out on the basis of the clinic and the Department of Infectious Diseases with Epidemiology of SamSMU. A clinical case of primary diffuse large-cell B-cell lymphoma of the central nervous system is presented. The patient's brain CT and MRI, cerebrospinal flui
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7

Crout, J. Richard. "A description of clinical pharmacology and the clinical pharmacologist." Clinical Pharmacology and Therapeutics 39, no. 4 (1986): 439. http://dx.doi.org/10.1038/clpt.1986.73.

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8

Parakhina, T. V., and U. I. Pryimych. "Weber-Christian Disease (Clinical Case Description)." PAIN. JOINTS. SPINE, no. 3.23 (January 5, 2017): 74–78. http://dx.doi.org/10.22141/2224-1507.3.23.2016.85011.

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9

Smirnova, L. A. Smirnova, and O. V. Simonova Simonova. "PARANEOPLASTIC DERMATOMYOSITIS: DESCRIPTION OF CLINICAL CASE." Pharmateca s2_2018 (May 3, 2018): 72–74. http://dx.doi.org/10.18565/pharmateca.2018.s2.72-74.

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10

Hamer, P. W., R. H. Holloway, R. Heddle, P. G. Devitt, and S. K. Thompson. "Type III achalasia—a clinical description." Diseases of the Esophagus 30, no. 8 (2017): 1–6. http://dx.doi.org/10.1093/dote/dox051.

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11

Westen, Drew, and Joel Weinberger. "When clinical description becomes statistical prediction." American Psychologist 59, no. 7 (2004): 595–613. http://dx.doi.org/10.1037/0003-066x.59.7.595.

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12

Shafik, Ahmed. "Deflation reflex: Description and clinical significance." Anatomical Record 249, no. 3 (1997): 405–8. http://dx.doi.org/10.1002/(sici)1097-0185(199711)249:3<405::aid-ar12>3.0.co;2-s.

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13

Bulatov, Al'bert R., Igor' V. Litvinenko, Nikolay V. Tsygan, et al. "Nodopathy: clinic, diagnosis, treatment. Clinical description." Russian Military Medical Academy Reports 42, no. 4 (2023): 427–35. http://dx.doi.org/10.17816/rmmar611154.

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AIM: Evaluation of the significance and possibilities of laboratory-instrumental diagnostic methods in establishing the diagnosis and selection of targeted therapy in patients with nodopathies.&#x0D; MATERIALS AND METHODS: System analysis of data from foreign and domestic literature with the presentation of a clinical case.&#x0D; RESULTS: Polyneuropathies are classified as demyelinating or axonal based on electrophysiological studies. However, in 2015, in addition to axonal and demyelinating neuropathies, it was proposed to distinguish a separate pathophysiological group — nodopathies. The pat
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14

Mościcka, Paulina, Justyna B. Cwajda, Arkadiusz Jawień, and Maria T. Szewczyk. "Crush wounds as an interdisciplinary problem: a description of two clinical cases." Surgical and Vascular Nursing 18, no. 4 (2024): 157–64. https://doi.org/10.5114/pchia.2024.146910.

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15

Takarangi, Melanie K. T., Jacinta M. Oulton, and Deryn Strange. "Explaining Memory Amplification: Is It All About the Test Format?" Clinical Psychological Science 6, no. 3 (2017): 394–406. http://dx.doi.org/10.1177/2167702617744326.

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Trauma-exposed people commonly exhibit a “memory amplification” effect, endorsing exposure to more traumatic events over time. Studies reporting this phenomenon have typically relied on checklists, where participants read event descriptions and indicate (yes/no) their exposure. We examined whether that approach is vulnerable to response biases and memory errors. In two experiments, participants viewed negative photos and completed an Old-New recognition test. In Experiment 1, participants completed either a photo recognition test or description test—composed of written descriptions of negative
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16

Galvão, Márcio Antônio Moreira, Cláudio Mafra, Chequer Buffe Chamone, Simone Berger Calic, Jorge E. Zavala-Velazquez, and David Hughes Walker. "Clinical and laboratorial evidence of Rickettsia felis infections in Latin America." Revista da Sociedade Brasileira de Medicina Tropical 37, no. 3 (2004): 238–40. http://dx.doi.org/10.1590/s0037-86822004000300009.

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After the discovery and initial characterization of Rickettsia felis in 1992 by Azad and cols, and the subsequent first description of a human case of infection in 1994, there have been two communications of human rickettsiosis cases caused by Rickettsia felis in Latin America. The first one was published in 2000 by Zavala-Velazquez and cols in Mexico. In 2001 Raoult and cols described the occurrence of two human cases of Rickettsia felis rickettsiosis in Brazil. In the present discussion these two articles were compared and after the description of the principal signs and symptoms, it was con
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17

Friedenberg, RM, JB Lightfoote, SP Wang, and MF Smolin. "Digital tomography: description and preliminary clinical experience." American Journal of Roentgenology 144, no. 3 (1985): 639–43. http://dx.doi.org/10.2214/ajr.144.3.639.

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18

Piccolo, Vincenzo, Teresa Russo, Lilian Mathias Delorenze, and Giuseppe Argenziano. "Perinevic dermatosis neglecta: clinical and dermoscopic description." Anais Brasileiros de Dermatologia 94, no. 3 (2019): 361–62. http://dx.doi.org/10.1590/abd1806-4841.20197980.

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19

Suryono, Suryono, and Nasronudin Nasronudin. "Clinical Description and Diagnosis of HIV/AIDS." Indonesian Journal of Tropical and Infectious Disease 5, no. 1 (2015): 23. http://dx.doi.org/10.20473/ijtid.v5i1.212.

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20

Buchinskaya, Natalia V., Eugenia A. Isupova, and Mikhail M. Kostik. "Homocystinuria: Literature Review and Clinical Case Description." Current Pediatrics 18, no. 3 (2019): 187–95. http://dx.doi.org/10.15690/vsp.v18i3.2036.

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Homocystinuria is rare autosomal-recessive monogenic disorder associated with disturbance of methionine metabolism due to liver enzyme cystathionine--synthetase (CBS) deficit. That in turn causes elevated concentration of homocystein and its metabolites in blood and urine. The main clinical manifestations of homocystinuria are: myopia, ectopia lentis, psychomotor retardation, learning difficulties, mental retardation, mental illnesses, behaviour problems, paroxysms, extrapyramidal symptoms, skeletal anomalies (body height), long limbs — dolichostenomelia and arachnodactylia (Marfan Phenotype),
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21

Comstock Barker, Paige, and Jennifer S. Scherer. "Illness Trajectories: Description and Clinical Use #326." Journal of Palliative Medicine 20, no. 4 (2017): 426–27. http://dx.doi.org/10.1089/jpm.2016.0554.

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22

Grandjean, Michael. "New Abdominal Acupuncture: Description With Clinical Examples." Medical Acupuncture 22, no. 3 (2010): 197–201. http://dx.doi.org/10.1089/acu.2009.0733.

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23

KISELEVA, T. A., D. R. ISLAMOVA, and K. R. BAGAUTDINOVA. "Insulinoma: literature review and clinical case description." Practical medicine 22, no. 4 (2024): 36–40. http://dx.doi.org/10.32000/2072-1757-2024-4-36-40.

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Insulinoma is a neuroendocrine tumor arising from β-cells of the islets of Langerhans, causing hypoglycemic attacks due to endogenous hyperinsulinism. The worldwide prevalence is approximately 1 case per 250,000–1,000,000 population, the incidence is 1–4 cases per million population per year. In most cases, the formation of insulinoma is sporadic (90%), less often it can be detected as part of the multiple endocrine neoplasia syndrome type 1 (10%). This review discusses the pathogenetic mechanisms of hypoglycemic syndrome, criteria for differential diagnosis, modern laboratory and imaging meth
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24

Belysheva, Tatiana S., Ekaterina E. Zelenova, Nataliya A. Semenova, et al. "Proteus Syndrome: Description of Two Clinical Cases." Current Pediatrics 23, no. 5 (2024): 343–49. http://dx.doi.org/10.15690/vsp.v23i5.2797.

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Background. Proteus syndrome is extremely rare congenital multisystem disease with high variability in clinical manifestations. Its prevalence is unknown, there are less than 200 cases in the world literature. The syndrome is a classic example of somatic mosaicism, and all target drugs for its management are based on it. Clinical case description. This article describes two clinical cases with somatic variants of the nucleotide sequence in the AKT1 gene, mosaic form, revealed by the NGS method. Target drug (mTOR-inhibitors group) was assigned in one case. Conclusion. The description of the phe
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25

GRISSO, THOMAS, and JUDITH QUINLAN. "Juvenile Court Clinical Services: A National Description." Juvenile and Family Court Journal 56, no. 4 (2005): 9–20. http://dx.doi.org/10.1111/j.1755-6988.2005.tb00175.x.

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26

Lopez, F., D. Muñoz, A. Mendoza, et al. "Electric sleep status: clinical and electroencephalographic description." Journal of the Neurological Sciences 357 (October 2015): e444. http://dx.doi.org/10.1016/j.jns.2015.09.088.

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27

Rajaraman, Revathi, Prajna Lalitha, Anita Raghavan, Manikandan Palanisamy, and Namperumalsamy Venkatesh Prajna. "Traumatic Lenticular Abscess: Clinical Description and Outcome." American Journal of Ophthalmology 144, no. 1 (2007): 144–46. http://dx.doi.org/10.1016/j.ajo.2007.02.040.

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28

Hupp, James R. "Digital tomography: Description and preliminary clinical experience." Journal of Oral and Maxillofacial Surgery 43, no. 10 (1985): 829. http://dx.doi.org/10.1016/0278-2391(85)90350-7.

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29

Shannon, Daniel C., David W. Carley Phd, and Dorothy H. Kelly. "Periodic breathing: Quantitative analysis and clinical description." Pediatric Pulmonology 4, no. 2 (1988): 98–102. http://dx.doi.org/10.1002/ppul.1950040207.

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30

Nikolaeva, D. S., A. N. Suinalieva, M. R. Shaidullina, L. S. Sozaeva, and M. A. Kareva. "Hippel-Lindau syndrome: description of clinical cases." Endocrine Surgery 17, no. 4 (2023): 71. http://dx.doi.org/10.14341/serg12893.

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31

R. Diaz Aguila, Hector. "Clinical Ultrasound. Essential tool for health care." Radiology Research and Diagnostic Imaging 2, no. 1 (2023): 01–05. http://dx.doi.org/10.58489/2836-5127/006.

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A brief description of the clinical iltrasound is presented; its definition; main indications; advantages as well as its weaknesses. The POCUS learning curve is pointed out for personnel without prior knowledge of it.
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32

Ingula, N. I. "Clinical management of patients with vertebral lumbosacral radiculopathy. Description clinical cases." East European Journal of Neurology, no. 3(3) (December 20, 2015): 49–53. http://dx.doi.org/10.33444/2411-5797.2015.3(3).49-53.

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Lumbosacral radiculopathy one of the most difficult choices vertebrogenic pain syndromes characterized especially intense and prolonged pain, usually accompanied by a sharp restriction of mobility, and is the most common cause of disability. Most of the destruction of roots of spinal nerves caused by vertebral reasons the presence of a herniated disc, degenerative changes in the intervertebral joints, narrow spinal canal. This article describes a clinical case of practice management of patients with chronic vertebral lumbosacral radiculopathy. The main causes of pain in the lower back, the mai
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33

Palma, J.-A., and F. Palma. "A probable cluster headache case from a textbook of 1726: Francisco Suárez de Rivera’s description." Cephalalgia 31, no. 11 (2011): 1232–35. http://dx.doi.org/10.1177/0333102411413161.

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Background: Few descriptions of cluster and cluster-like headache made before the 19th century have been reported. Case description: We present a previously unreported early description of a probable cluster headache case made by Francisco Suárez de Rivera (1686− c.1751), one of the main physicians of the Spanish Age of Enlightenment, writer of almost 40 textbooks about medicine, surgery, pharmacology, and therapeutics. Discussion: The depiction here reported of a woman with probable cluster headache is possibly one of the earliest known and, to our knowledge, the first in Hispanic literature.
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34

Stilidi, I. S., E. R. Charchyan, K. I. Zhordania, V. J. Bokhian, N. A. Kozlov, and J. G. Pajanidi. "Intracardiac intravenous leiomyomatosis: description of a clinical case." Clinical and Experimental Surgery. Petrovsky journal 9, no. 1 (2021): 70–76. http://dx.doi.org/10.33029/2308-1198-2021-9-1-70-76.

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35

Komarova, L. N., E. I. Berzina, S. A. Zvezda, et al. "Cold agglutinin disease. Description of the clinical case." Medical Science And Education Of Ural 21, no. 4 (2020): 62–64. http://dx.doi.org/10.36361/1814-8999-2020-21-4-62-64.

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The article presents a clinical case of admission, observation and treatment of a senior patient with a diagnosis: Primary (idiopathic) cold agglutinin disease. Coronary heart disease. Exertional angina pectoris. Functional class 1. One of the rather rare and non-standard diagnoses in the work of a clinical doctor on duty is presented. A spectrum of examinations of the blood from patients with this disease was presented. Cold agglutinin disease (CAD) is an autoimmune hemolytic anemia in which immunoglobulin M antibodies bind to red blood cells and fix complement, which leads to the development
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36

Cherednichenko, M. M., T. G. Zadorkina, N. V. Nekrasova, and E. M. Ovechkina. "Hereditary pigmentary dermatopathy (description of the clinical case)." Смоленский медицинский альманах, no. 2 (2022): 148–52. http://dx.doi.org/10.37903/sma.2022.2.30.

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37

Evseeva, A. L., S. V. Koshkin, V. V. Ryabova, and O. S. Kovrova. "Eixtragenital primary syphilis: a description of clinical cases." Vestnik dermatologii i venerologii 94, no. 5 (2019): 72–76. http://dx.doi.org/10.25208/0042-4609-2018-94-5-72-76.

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38

Dudnyk, V. M., V. G. Furman, O. V. Kutsak, and O. I. Izyumets. "Heritable amegacariocytic thrombocytopenia: description of a clinical case." Reports of Vinnytsia National Medical University 26, no. 1 (2022): 27–30. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(1)-04.

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Annotation. Features of the clinical course and differential diagnosis of hereditary thrombocytopenia, characterized by the development of pancytopenia in childhood, are described. It was found that the main manifestation of this pathology is hemorrhagic syndrome, accompanied by the presence of polymorphic, polychrome, asymmetric hemorrhagic rashes, frequent bleeding from the mucous membranes. The Mpl gene (1p34) was sequestered to confirm the diagnosis and establish the genomic mutation. Complex diagnosis of this disease requires a comprehensive and interdisciplinary approach involving a coor
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39

Dudnyk, V. M., V. G. Furman, O. V. Kutsak, and O. I. Izyumets. "Heritable amegacariocytic thrombocytopenia: description of a clinical case." Reports of Vinnytsia National Medical University 26, no. 1 (2022): 27–30. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(1)-04.

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Annotation. Features of the clinical course and differential diagnosis of hereditary thrombocytopenia, characterized by the development of pancytopenia in childhood, are described. It was found that the main manifestation of this pathology is hemorrhagic syndrome, accompanied by the presence of polymorphic, polychrome, asymmetric hemorrhagic rashes, frequent bleeding from the mucous membranes. The Mpl gene (1p34) was sequestered to confirm the diagnosis and establish the genomic mutation. Complex diagnosis of this disease requires a comprehensive and interdisciplinary approach involving a coor
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40

Kocabaş, Engin, Gülsüm Gençoğlan, Ferdi Öztürk, and Aylin Türel Ermertcan. "Halo angioma: A new clinical and dermoscopical description." European Journal of Dermatology 21, no. 4 (2011): 617–18. http://dx.doi.org/10.1684/ejd.2011.1328.

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41

АКЧУРИН, С. В., Г. П. ДЮЛЬГЕР, И. В. АКЧУРИНА, В. С. БЫЧКОВ, and Е. С. ЛАТЫНИНА. "RECOMMENDATIONS FOR THE DESCRIPTION OF VETERINARY CLINICAL CASES." VESTNIK RIAZANSKOGO GOSUDARSTVENNOGO AGROTEHNOLOGICHESKOGO UNIVERSITETA IM P A KOSTYCHEVA, no. 4(48) (December 29, 2020): 5–10. http://dx.doi.org/10.36508/rsatu.2020.48.4.001.

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Проблема и цель. Проблемой в системе высшего ветеринарного образования является дефицит ветеринарных клинических кейсов на русском языке, находящихся в свободном доступе, что оказывает негативное влияние на процесс непрерывного повышения качества подготовки студентов ветеринарных специальностей и повышения квалификации практикующих врачей. Библиометрический анализ публикаций, проведенный по материалам библиотеки eLIBRARY, позволил установить, что доля работ, посвященных использованию кейсов в ветеринарии, в общем количестве публикаций на тему кейсов составляет всего 0,04 %. Целью настоящего ис
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42

PA, Leye, Malissin I, Mora P, Voicu S, Elgharbi F, and Megarbane B. "Refractory Myasthenia Gravis: Clinical Description and Literature Review." Scholars Journal of Applied Medical Sciences 08, no. 01 (2020): 171–73. http://dx.doi.org/10.36347/sjams.2020.v08i01.033.

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43

Ferral, Hector. "Hydrogel-Coated Coils: Product Description and Clinical Applications." Seminars in Interventional Radiology 32, no. 04 (2015): 343–48. http://dx.doi.org/10.1055/s-0035-1564809.

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44

Miller, Linda T., Cheryl A. Missiuna, Jennifer J. Macnab, Theresa Malloy-Miller, and Helene J. Polatajko. "Clinical Description of Children with Developmental Coordination Disorder." Canadian Journal of Occupational Therapy 68, no. 1 (2001): 5–15. http://dx.doi.org/10.1177/000841740106800101.

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45

Borsa, R., M. Governa, G. Aimé, D. Fraire, E. Baralis, and G. Fontana. "Penetrating bladder injuries: Description of a clinical case." Urologia Journal 62, no. 1_suppl (1995): 190–91. http://dx.doi.org/10.1177/039156039506201s51.

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— A penetrating bladder injury in a youth due to impalement through the scrotum was successfully operated. Perforation was at the bottom and on the dome and the absence of a clinical uro-peritoneal picture was due to the plugging of the latter rupture by the omentum. Retrograde urethrocystography was negative and only pelvic ultrasound characterised the diagnosis, leading to an immediate explorative surgical approach.
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46

Marszal, Elzbieta, Ewa Jamroz, Jacek Pilch, Ewa Kluczewska, Halina Jablecka-Deja, and Robert Krawczyk. "Agenesis of Corpus Callosum: Clinical Description and Etiology." Journal of Child Neurology 15, no. 6 (2000): 401–5. http://dx.doi.org/10.1177/088307380001500609.

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47

Lau, William, and David Pye. "A Clinical Description of Ocular Response Analyzer Measurements." Investigative Opthalmology & Visual Science 52, no. 6 (2011): 2911. http://dx.doi.org/10.1167/iovs.10-6763.

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48

Weidman, Hazel H. "Stylistic Aspects of Clinical Anthropology: A Mirrored Description." Medical Anthropology Newsletter 16, no. 3 (1985): 63–64. http://dx.doi.org/10.1525/maq.1985.16.3.02a00040.

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49

Weidman, Hazel H. "Stylistic Aspects of Clinical Anthropology: A Mirrored Description." Medical Anthropology Quarterly 16, no. 3 (1985): 63–64. http://dx.doi.org/10.1111/j.1937-6219.1985.tb00982.x.

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50

Panchuk, Yu P., M. Yu Yaroslavtsev, A. A. Polonnikova, et al. "Peripartal cardiomyopathy: literature review and clinical case description." Bulletin of the Medical Institute "REAVIZ" (REHABILITATION, DOCTOR AND HEALTH) 14, no. 3 (2024): 89–95. http://dx.doi.org/10.20340/vmi-rvz.2024.3.case.2.

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The cardiovascular system during pregnancy undergoes a number of compensatory and adaptive changes, such as an increase in heart rate, cardiac output and total peripheral resistance, which causes an increase in the load on the myocardium. Peripartum cardiomyopathy is a serious polyetiological complication of pregnancy and the postpartum period, as well as an important cause of disability and mortality for both mother and fetus. The non-specificity of complaints and the paucity of clinical symptoms in the early stages of the disease lead to delayed diagnosis and significantly increase the frequ
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