نتایج جستجو برای: citrullinemia

تعداد نتایج: 234  

2013
Isabelle Marie Pierre-Yves Hatron Patrick Cherin Eric Hachulla Elisabeth Diot Olivier Vittecoq Jean-François Menard Fabienne Jouen Stéphane Dominique

INTRODUCTION The aims of this present study were firstly to assess the outcome, including functional course, in anti-Jo1 positive patients with antisynthetase syndrome (ASS), and secondly to determine predictive parameters of poor outcome in these patients. METHODS The medical records of 86 consecutive anti-Jo1 patients with ASS were reviewed in 4 academic centers. RESULTS 13 patients (15.1...

2006
R. Lima

We st udy t he evolution of a coupled map la t t ice in two dimensions with st rong coupling. We show t he tenden cy of such system to ass ume (quas i) homogeneous space configur a t ions evolving in time. We describe the mechanism of t his phenomen on. Coupled Map Lat ti ces (CM Ls), which were int roduced rather recently [1, 2], now serve as one of the most useful and powerful instruments for...

Journal: :The Turkish journal of pediatrics 2017
Berna Şeker-Yılmaz Deniz Kör Gökhan Tümgör Serdar Ceylaner Neslihan Önenli-Mungan

Şeker-Yılmaz B, Kör D, Tümgör G, Ceylaner S, Önenli-Mungan N. p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency. Turk J Pediatr 2017; 59: 311-314. Citrin deficiency is an autosomal recessive metabolic disorder, which is caused by pathogenic mutations in the SLC25A13 gene on chromosome 7q21.3, as the causative gene that encodes the liver type aspartate/glutama...

2007
IAN J. HOPKINS JOHN F. CONNELLY

Accumulation of ammonia in body tissues most commonly occurs in hepatic failure. However, it may also result from a specific deficiency of an enzyme of the urea cycle (Fig., 1). Severe hyperammonaemia has been reported with deficiencies of carbamyl phosphate synthetase (Freeman et al., 1964) and ornithine transcarbamylase (Russell et al., 1962; Levin and Russell, 1967). Some increase in blood a...

2016
Neng-Li Wang Yu-Lan Lu Ping Zhang Mei-Hong Zhang Jing-Yu Gong Yi Lu Xin-Bao Xie Yi-Ling Qiu Yan-Yan Yan Bing-bing Wu Jian-She Wang

BACKGROUND AND AIMS Large indels are commonly identified in patients but are not detectable by routine Sanger sequencing and panel sequencing. We specially designed a multi-gene panel that could simultaneously test known large indels in addition to ordinary variants, and reported the diagnostic yield in patients with intrahepatic cholestasis. METHODS The panel contains 61 genes associated wit...

Journal: :AJNR. American journal of neuroradiology 2008
T Niwa N Aida A Shishikura K Fujita T Inoue

BACKGROUND AND PURPOSE MR susceptibility-weighted imaging (SWI) is a highly sensitive technique for detection of hemorrhage, but its utility in the evaluation of children with laminar necrosis is not yet known. We assessed whether cortical laminar necrosis in pediatric patients contains hemorrhage on SWI. MATERIALS AND METHODS "Cortical laminar necrosis" was defined as a hyperintense cortical...

2012
Ines Lakhal-Naouar Armando Jardim Rona Strasser Shen Luo Yukiko Kozakai Hira L. Nakhasi Robert C. Duncan

BACKGROUND Gene expression analysis in Leishmania donovani (Ld) identified an orthologue of the urea cycle enzyme, argininosuccinate synthase (LdASS), that was more abundantly expressed in amastigotes than in promastigotes. In order to characterize in detail this newly identified protein in Leishmania, we determined its enzymatic activity, subcellular localization in the parasite and affect on ...

2017
Ivan Ivanovski Miloš Ješić Ana Ivanovski Livia Garavelli Petar Ivanovski

The underlying pathophysiology of liver dysfunction in urea cycle disorders (UCDs) is still largely elusive. There is some evidence that the accumulation of urea cycle (UC) intermediates are toxic for hepatocyte mitochondria. It is possible that liver injury is directly caused by the toxicity of ammonia. The rarity of UCDs, the lack of checking of iron level in these patients, superficial knowl...

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