نتایج جستجو برای: klinefelters syndrome

تعداد نتایج: 621914  

Journal: :iranian journal of child neurology 0
seyed hassan tonekaboni 1. professor of pediatric neurology, pediatric neurology research center, shahid beheshi university of medical science, tehran, iran 2. professor of pediatric neurology, school of medicine, hahid beheshi university of medical science, tehran, iran ahmad ebrahimi phd of medical genetic, parseh medical genetics center, tehran, iran mohammadkazem bakhshandeh bali pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran massoud houshmand phd of medical clinical genetic, national institute of genetic engineering and biotechnology, tehran, iran mehdi moghaddasi neurologist, department of neurology, rasool-e-akram hospital, tehran university of medical sciences, tehran, iran mohammad mahdi taghdiri associate professor of pediatric neurology, shahid beheshti university of medical science, tehran, iran

how to cite this article: tonekaboni sh, ebrahimi a, bakhshandeh bali mk, houshmand m, moghaddasi m, taghdiri mm, nasehi mm. sodium channel gene mutations in children with gefs + and dravet syndrome: a cross sectional study. iran j child neurol. 2013 winter; 7 (1):25-29.   objective dravet syndrome or severe myoclonic epilepsy of infancy (smei) is a baleful epileptic encephalopathy that begins ...

Journal: :journal of pediatrics review 0
javad ghaffari antimicrobial nosocomial research center, mazandaran university of medical sciences, sari, iran hamid ahanchian allergy research center, mashhad university of medical sciences, mashhad, iran fariborz zandieh faculty of medicine, tehran university of medical sciences, tehran, iran

hyper ige syndrome (hies) is a rare primary immunodeficiency disease. most of hies cases are sporadic. hies type ad is caused by mutation in signal transducer and activator of transcription-3 (stat-3). a number of mosaicism hies has been reported that is associated with intermediate phenotype. autosomal recessive hies (ar-hies) is due to mutation in dock-8 or cytokine sis 8 and tyk2 or tyrosine...

Journal: :journal of research in medical sciences 0
behnaz khani assistant professor, department of obstetrics and gynecology, school of medicine, isfahan university of medical sciences, isfahan, iran ferdous mehrabian associate professor, obstetrics and gynecology department, school of medicine, isfahan university of medical science, isfahan, iran elaheh khalesi department of obstetrics and gynecology, school of medicine, isfahan university of medical sciences, isfahan, iran azadeh eshraghi school of pharmacy, isfahan university of medical sciences, isfahan, iran

background: phytoestrogens are a group of plants derived compounds with weekly estrogen effect that appear to have protective effects on metabolic and hormonal abnormalities of women with polycystic ovary syndrome (pcos). so the aim of this study was to investigate the effect of soy phytoestrogens on reproductive hormones and lipid profiles in pcos women. methods: in this quasi-randomized trial...

Journal: :journal of research in medical sciences 0
mehrzad salmasi laya amini shaghayegh haghjooy javanmard mohammad saadatnia

background: the correlation of metabolic syndrome and migraine headache was evaluated in some previous studies. however there is no study that compared the prevalence of metabolic syndrome in the patients with and without migraine. control of coincidental factors such as metabolic syndrome reduces therapeutic resistance in migrainous patients. the aim of this study was to compare prevalence of ...

ژورنال: رویش روانشناسی 2019

This study examined the relationship of academic stress and social anxiety in students and its role in predicting the imposter syndrome. Its design is Correlation research and the sample consisted of 160 male and female students who were selected by cluster sampling. They respond to academic stress (LASRS), social anxiety (SPIN) and imposter syndrome (CIPS) questionnaire.  Data analysis was...

Journal: :hepatitis monthly 0
dondu uskudar cansu division of rheumatology, department of internal medicine, eskisehir osmangazi university, eskisehir, turkey; department of rheumatology, school of medicine, eskisehir osmangazi university eskisehir, turkey. tel: +90-2222392979-2931, fax: +90-2222393772 tuncer temel division of gastroenterology, department of internal medicine, eskisehir osmangazi university, eskisehir, turkey adem erturk division of rheumatology, department of internal medicine, eskisehir osmangazi university, eskisehir, turkey timucin kasifoglu division of rheumatology, department of internal medicine, eskisehir osmangazi university, eskisehir, turkey berat acu department of radiology, eskisehir osmangazi university, eskisehir, turkey cengiz korkmaz division of rheumatology, department of internal medicine, eskisehir osmangazi university, eskisehir, turkey

conclusions in our study, portal venous thrombosis was detected in the patient who died during the acute period only. a study including large numbers of budd-chiari-syndrome patients with behcet’s disease and portal venous thrombosis would be helpful to determine the prognostic significance of portal venous thrombosis in budd-chiari-syndrome patients with behcet’s disease. in addition, patients...

Journal: :مجله دانشکده پرستاری و مامایی ارومیه 0
سعید حسین پور s hosseinpoor فتح الله غلامی بروجنی f gholamiborujeni یوسف محمدیان y mohammadian

modeling of relationship between ventilation rate of buildings and sick building syndrome symptoms hosseinpoor s , gholamiborujeni f *, mohammadian y received: 22 aug, 2013 accepted: 23 oct , 2013 abstract background & aims: indoor air pollution with microbilal, chemical and physical pollutants lead to sick building syndrome (sbs). suitable ventilation of buildings, is one of the best methods t...

Journal: :iranian journal of medical sciences 0
r. vakili m. horri

turner syndrome is a sex-chromosome disorder occurring in one out of 2500 female births and characterized by growth retardation, gonadal dysgenesis and cardiovascular anomalies. the 45, xo karyotype is the most frequent type of this disease. herein, we report on a 6-year-old girl with turner syndrome and 45, xo karyotype presenting with short stature. she had dextrocardia and hiatal hernia. to ...

Journal: :مجله بین المللی کودکان و نوجوانان 0
hasan otukesh iran university of medical sciences rozita hoseini iran university of medical sciences parnian kheirkhah rahimabad iran university of medical sciences mitra mehrazma iran university of medical sciences

background: nephrotic syndrome and type 1 diabetes mellitus are two common chronic conditions in children. co-existence of these conditions is an extremely rare finding. case presentation: this report presents a 6-year-old boy who was diagnosed with nephrotic syndrome five years ago and type 1 diabetes mellitus in infancy. renal biopsy showed membranous glomerulonephritis, which is a rare histo...

Journal: :medical journal of islamic republic of iran 0
mojtaba tabarestani from tile department of clinical pathology, imam reza hospital, mashhad university of medical sciences, mashhad, islamic republic of iran.

hemophagocytic syndrome is a non-malignant process that is characterized clinically by fever, hepatomegaly, splenomegaly, pancytopenia in peripheral blood, and reactive histiocytes in the bone marrow. bacterial infectious diseases like typhoid fever and brucellosis and viral infections including cmv, herpes viruses, and epstein-barr virus are diagnosed as the cause of this syndrome. in this pap...

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