Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare
autosomal recessive tubular disorder caused by CLDN16 mutations. CLDN16 encodes the renal …

Rituximab has been used over the last decade as a rescue therapy for refractory cases of
nephrotic syndrome (NS). Here we report the use of rituximab in four children with idiopathic …

… Hammad O. Alshaya … & Alshaya, HO Familial hypomagnesemia with hypercalciuria
and nephrocalcinosis. Pediatr Nephrol 18, 506–510 (2003). https://doi.org/10.1007/s00467-003-1139…

Abstract Treatment of steroid-resistant nephrotic syndrome (SRNS) remains a challenge to
pediatric nephrologists. Recently, intravenous cyclophosphamide (IV-CPM) infusion was …

Objectives: To evaluate the effectiveness of levamisole in maintaining remission in children
with steroid-sensitive nephrotic syndrome (SSNS) who had a frequent relapsing or steroid-…

Mitochondria are essential for the homeostasis of every cell except red blood cells. 1 Therefore,
mitochondrial disorders cause a wide range of clinical presentations; however, organs …

Objective: The objective of this study is to evaluate the first aid (FA) knowledge, practice,
and attitude of medical and nursing students at Taibah University in Madinah. Methods: The …

Background Atherosclerotic cardiovascular disease (ASCVD), heart failure (HF), chronic
kidney disease (CKD), and obesity are associated with increased morbidity and mortality in …

Background Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC)
is a rare autosomal recessive tubular disorder that eventually progresses to renal failure, …

Aim. To analyze the distribution and characteristics of infraocclusion among Arabian children
in primary dentition and its associated dental anomalies. Methods. A radiographic analysis …