نتایج جستجو برای: behcets syndrome diagnosis

تعداد نتایج: 1029070  

Journal: :Case Reports in Gastroenterology 2020

p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; text-align: justify; font: 12.0px 'Times New Roman'} span.s1 {text-decoration: underline} span.s2 {font: 11.0px Helvetica} Introduction: Polycystic ovary syndrome (PCOS) in adults is diagnosed based on clinical, biochemical, and radiological criteria, although in adolescents, some of these criteria may overlap with the normal process of puberty, which ...

Journal: :archives of pediatric infectious diseases 0
mojtaba kamali aghdam department of pediatrics, zanjan university of medical sciences, zanjan, ir iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی زنجان (zanjan university of medical sciences) kambiz eftekhari department of pediatrics, zanjan university of medical sciences, zanjan, ir iran; pediatric ward, ayatollah mousavi hospital, zanjan, ir iran. tel: +98-24141310001, fax: +98-2414131340سازمان اصلی تایید شده: دانشگاه علوم پزشکی زنجان (zanjan university of medical sciences)

toxic shock syndrome in children following infection with influenza is a very rare syndrome. if it is not diagnosed quickly, it may cause significant morbidity and mortality. for diagnosis of toxic shock syndrome, clinical and laboratory criteria are used. our patient is a 3.5-year old boy who admitted to the hospital with high fever, weakness, toxicity, hypotension and skin rash due to influen...

GR ZAMANI, M GHOFRANI,

MELAS syndrome is a mitochondrial disorder with progressive nature, because adequate treatment is not available. Diagnosis of this mitochondrial disorder depends initially on clinical suspicion, which is strengthened by additional metabolic evidence of impaired oxidative metabolism such as high serum or C.S.F. lactate levels and confirmed by demonstration of mitochondrial abnormalities-in ...

AR Alihosseini MM Kooshyar

Proteus syndrome is a rare congenital disorder comprised of subcutaneous and internal hamartomas, miscellaneous skin and vascular nevi, skeletal and nervous system and eye malformations, with characteristic manifestations including hemihypertrophy, local gigantism, macrodactyly and cerebriform thickness of soles and palms. A 23 year-old man with diagnosis of proteus syndrome had sever ane...

Journal: :The Journal of Laryngology & Otology 2016

Journal: :Journal of Medical Genetics 1992

Journal: :CHRISMED Journal of Health and Research 2015

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