نتایج جستجو برای: early onset

تعداد نتایج: 826058  

A. Peirovifar G.A. Maamuri H. Boskabadi J.T. Afshari M.M. Gharehbaghi, M.T. Shakeri

Background: The purpose of this study was to determine the relationship between early onset sepsis and increased levels of C-reactive protein (CRP) and interleukin-6 (IL-6) in cord plasma. Methods: A prospective study was conducted in 141 premature infants delivered with gestational ages of 26-35 weeks. IL-6 and CPR were measured by enzyme-linked immunoassay in the cord plasma of the neonates. ...

سید محمد میلانی, ,

Background: To identify the clinical manifestations and mortality rate among neonates with early- and late-onset sepsis.Methods: We retrospectively reviewed the hospital records in Children’s Hospital Medical Center, Tehran University of Medical Sciences of 104 neonates (50 females and 54 males) diagnosed with septicemia and treated from September 1994 to August 1995. Diagnosis of septicemia wa...

Background The X-linked cyclin-dependent kinase like 5 (CDKL5/STK9) gene has been shown to be responsible for a severe encephalopathy condition characterized by early onset of epilepsy and severe developmental delay. CDKL5 mutations have been shown to be more frequent among female patients. Results Here we report a 6- month male patient, second child of a healthy non consanguineous in the Irani...

Journal: :genetics in the 3rd millennium 0
شهره زارع کاریزی shohreh i zare kariz akbari medical genetics laboratory, tehran, iran1- آزمایشگاه ژنتیک پزشکی دکتر اکبری، تهران، ایران محمد تقی اکبری mohammad taghi akbari akbari medical genetics laboratory, tehran, iran. department of medical genetics, tarbiat modares university, tehran, iran1- آزمایشگاه ژنتیک پزشکی دکتر اکبری، تهران، ایران.بخش ژنتیک پزشکی، دانشگاه تربیت مدرس، تهران، ایران غلامرضا شهیدی gholamreza shahidi iran university ofدانشگاه علوم پزشکی ایران، تهران، ایران زهرا بهمنی zahra bahmani akbari medical genetics laboratory, tehran, iran1- آزمایشگاه ژنتیک پزشکی دکتر اکبری، تهران، ایران

early-onset, generalized primary torsion dystonia (ptd) is an autosomal dominant disorder, characterized by involuntary movements and abnormal postures. the majority of cases are caused by a 3-bp deletion (gag deletion at position 946) in the dyt1 gene on chromosome 9q34 that allows for specific genetic testing. forty eight patients with early onset primary torsion dystonia were screened for th...

Objective: Temporal Lobe Epilepsy (TLE) can contribute to various emotional symptoms by damaging the temporal lobe. This study aimed at investigating emotion processing in patients with early- and late-onset TLE compared to a healthy group. Methods: In this causal-comparative study, 60 patients with diagnosed TLE were compared to 60 healthy controls to identify emotion processing styles. The d...

Journal: :veterinary research forum 2014
maede moosavi abdolah mirzaei mohsen ghavami amin tamadon

the aim of the present study was to compare the occurrence and duration of clinical mastitis in different seasons, stages of lactation period and parities in a holstein dairy farm in iran. a retrospective epidemiological survey from april 2005 to march 2008 was conducted on 884 clinical mastitis cases of 7437 lactations. data of each case including calendar-date of mastitis onset, days in milk ...

Journal: :Neurologic Clinics 2017

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