Hypothesis: Primary nephrotic syndrome is a common renal pediatric disorder. We investigated allelic frequencies and genotypes of Endothelin (EDN1) rs5370 polymorphism among children with primary NS. Methods: A case control study was conducted in Mansoura University Children’s Hospital, Egypt during the period from December 2015 to January 2018. We included 50 steroid sensitive NS (SSNS) and 50 steroid resistant NS (SRNS) in addition to 100 healthy controls. All patients were assessed clinically and investigated for serum albumin, cholesterol, creatinine and urea, and 24-h urinary protein. We investigated all groups for EDN1 rs5370 genotypes (GG, GT and TT) and alleles (G and T) using polymerase chain reaction amplification-refractory mut...
To investigate the role of the reninangiotensin system genes polymorphisms in develop and progressio...
Advances in genome science in the last 20 years have led to the discovery of over 50 single gene cau...
The aim of this study was to elucidate whether genetic screening test results of pediatric patients ...
Hypothesis: Primary nephrotic syndrome is a common renal pediatric disorder. We investigated alleli...
Hypothesis: Primary nephrotic syndrome is a common renal pediatric disorder. We investigated alleli...
AbstractAimsThis study aims to investigate the relationship between plasma endothelin-1 (ET-1) conce...
BackgroundThe presence of endothelial dysfunction (ED) constitutes an early risk factor for cardiova...
Objective: This study was conducted to determine the frequency of C3435T and G2677T/C single nucleot...
A decreased GFR in the range of mild renal insufficiency and an increased urinary albumin excretion ...
International audienceBackground Steroid-sensitive nephrotic syndrome (SSNS) is a childhood disease ...
Background: Steroid resistant nephrotic syndrome (SRNS) is a rare condition, accounting for 10–15% o...
BACKGROUND: Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of end-sta...
Context: Nephrotic syndrome is one of the commonest renal problem encountered in children. It is d...
BACKGROUND: WT1 is one of the genes commonly reported as mutated in children with steroid-resistant ...
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the presence ...
To investigate the role of the reninangiotensin system genes polymorphisms in develop and progressio...
Advances in genome science in the last 20 years have led to the discovery of over 50 single gene cau...
The aim of this study was to elucidate whether genetic screening test results of pediatric patients ...
Hypothesis: Primary nephrotic syndrome is a common renal pediatric disorder. We investigated alleli...
Hypothesis: Primary nephrotic syndrome is a common renal pediatric disorder. We investigated alleli...
AbstractAimsThis study aims to investigate the relationship between plasma endothelin-1 (ET-1) conce...
BackgroundThe presence of endothelial dysfunction (ED) constitutes an early risk factor for cardiova...
Objective: This study was conducted to determine the frequency of C3435T and G2677T/C single nucleot...
A decreased GFR in the range of mild renal insufficiency and an increased urinary albumin excretion ...
International audienceBackground Steroid-sensitive nephrotic syndrome (SSNS) is a childhood disease ...
Background: Steroid resistant nephrotic syndrome (SRNS) is a rare condition, accounting for 10–15% o...
BACKGROUND: Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of end-sta...
Context: Nephrotic syndrome is one of the commonest renal problem encountered in children. It is d...
BACKGROUND: WT1 is one of the genes commonly reported as mutated in children with steroid-resistant ...
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the presence ...
To investigate the role of the reninangiotensin system genes polymorphisms in develop and progressio...
Advances in genome science in the last 20 years have led to the discovery of over 50 single gene cau...
The aim of this study was to elucidate whether genetic screening test results of pediatric patients ...