نتایج جستجو برای: schilder disease

تعداد نتایج: 1490288  

2015
Ana Carolina Coan Brunno M. Campos Felipe P.G Bergo Bruno Y. Kubota Clarissa L. Yasuda Marcia E. Morita Carlos A.M Guerreiro Fernando Cendes

Objective: Patients with mesial temporal lobe epilepsy (MTLE) may present unstable pattern of seizures. We aimed to evaluate the occurrence of relapse-remitting seizures in MTLE with (MTLE-HS) and without (MTLE-NL) hippocampal sclerosis. Method: We evaluated 172 patients with MTLE-HS (122) or MTLE-NL (50). Relapse-remitting pattern was defined as periods longer than two years of seizure-freedom...

Journal: :iranian journal of child neurology 0
mohammad ghofrani 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2.pediatric neurology center of excellence & pediatric neurology department sciences, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: ghofrani m. lysosomal storage disease (lsds). iran j child neurol. 2015 autumn;9:4(suppl.1): 1. pls see pdf.

Journal: :middle east journal of digestive diseases 0
kourosh masnadishirazi mohammad hossein somi yoosef bafandeh firooz saremi nooshin mylanchy parisa rezaeifar

background there are few reports from iran about the epidemiology and clinical features of inflammatory bowel disease (ibd). this study aims to determine the epide­miologic profile and clinical features of ibd in northwest iran referral centers. methods in a cross-sectional setting, we evaluated 200 patients with definitive diagno­ses of ibd who referred to tabriz educational hospitals during t...

Journal: :iranian red crescent medical journal 0
meltem erol department of pediatrics, bagcilar training and research hospital, istanbul, turkey; corresponding author: meltem erol, department of pediatrics, bagcilar training and research hospital, istanbul, turkey. tel: +90-5324578397, fax: +90-2124404242, e-mail: ozlem bostan gayret department of pediatrics, bagcilar training and research hospital, istanbul, turkey ozgul yigit department of pediatrics, bagcilar training and research hospital, istanbul, turkey kubra serefoglu cabuk department of ophtalmology, bagcilar training and research hospital, istanbul, turkey mehmet toksoz department of radiology, bagcilar training and research hospital, istanbul, turkey mahir tiras department of pediatrics, bagcilar training and research hospital, istanbul, turkey

conclusions in cases of unusual vascular lesions, metabolic diseases must be considered. in homocystinuria, early diagnosis and treatment are important. blood homocysteine levels can be returned to normal, and some complications can be prevented. introduction homocystinuria is a hereditary disease caused by a defect in the enzymes involved in metabolizing methionine. homocystinuria can influenc...

Journal: :مجله علوم اعصاب شفای خاتم 0
safieh ebrahimi department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran mohammad jalili-nik department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran hossein abde-ahad department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran mahdi hassanian department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran

thrombin is a multifunctional enzyme which has key roles in coagulation cascade and inflammatory events. the pro-inflammatory functions of thrombin occur by different mechanisms including increasing mast cell degranulation, up-regulating the expression of cell adhesion molecules (cams) and promoting the secretion of inflammatory chemokines and cytokines. dysregulated signaling functions of thro...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان فارس - دانشکده دندانپزشکی 1387

چکیده ندارد.

Journal: :Archives of disease in childhood 1971
C C Forsyth M Forbes J N Cumings

Forsyth, C. C., Forbes, M., and Cumings, J. N. (1971). Archives of Disease in Childhood, 46, 273. Adrenocortical atrophy and diffuse cerebral sclerosis. A boy, diagnosed as having Addison's disease due to idiopathic atrophy of the adrenal glands at the age of 7 years, developed the first evidence of what was originally thought to be 'Schilder's disease' at 8 years and 10 months. He died at 9 ye...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid behesti university of medical sciences, tehran, iran 2. department of pediatric neurology, pediatric neurology center of excellence, faculty of medicine, mofid children hospital, shahid behesti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p. pelizaeus-merzbacher- disease (pmd) and pelizaeus-merzbacher-like disease (pmld). iran j child neurol autumn 2014;8:4 (suppl.1):9-10.   pls see pdf.

2015
Rita Jacobs Patrick M Honore Herbert D Spapen

We read with great interest the paper by Schilder and colleagues on citrate anticoagulation versus systemic heparinisation (CASH) [1] and its related commentary [2], but would like to comment on two important metabolic issues. First, in-circuit ionized calcium was not monitored in the CASH trial. Keeping postfilter ionized calcium within tight limits, however, results in more optimal anticoagul...

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