about
Cystinosis: a reviewImmunomodulatory Effects of Chitotriosidase EnzymeCystinosis (ctns) zebrafish mutant shows pronephric glomerular and tubular dysfunction.Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic Cystinosis.Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis.Nephropathic cystinosis: an update.Cystinosin deficiency causes podocyte damage and loss associated with increased cell motility.Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report.Lysosomal Storage Disorders in Egyptian Children.Pituitary adenylate cyclase-activating polypeptide (PACAP) in zebrafish models of nephrotic syndrome.Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.Blood spot versus plasma chitotriosidase: a systematic clinical comparison.Ca(2+) signalling in human proximal tubular epithelial cells deficient for cystinosin.Association of chitotriosidase enzyme activity and genotype with the risk of nephropathy in type 2 diabetes.Altered mTOR signalling in nephropathic cystinosis.A Human Proximal Tubular Epithelial Cell Model to Explore a Knowledge Gap on Neonatal Drug Disposition.Plasma chitotriosidase and carotid intima-media thickness in children with sickle cell disease.Effect of Storage Conditions on Stability of Ophthalmological Compounded Cysteamine Eye Drops.Connective tissue growth factor (CTGF) from basics to clinics.Genetic Renal Diseases: The Emerging Role of Zebrafish ModelsAllogeneic HSCT transfers wild-type cystinosin to nonhematological epithelial cells in cystinosis: First human reportMolecular Basis of Cystinosis: Geographic Distribution, Functional Consequences of Mutations in the CTNS Gene, and Potential for RepairClinical, biomarker and genetic spectrum of Niemann-Pick type C in Egypt: The detection of nine novel NPC1 mutationsEnhanced Intrinsic Skin Aging in Nephropathic Cystinosis Assessed by High-Definition Optical Coherence TomographyChitotriosidase as a Novel Biomarker for Therapeutic Monitoring of Nephropathic CystinosisAPOL1 Risk Genotypes Are Associated With Early Kidney Damage in Children in Sub-Saharan AfricaCell-Based Phenotypic Drug Screening Identifies Luteolin as Candidate Therapeutic for Nephropathic CystinosisNovel biomarkers for lysosomal storage disorders: metabolomic and proteomic approaches
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mohamed A Elmonem
@nl
Mohamed A Elmonem
@sl
Mohamed A. Elmonem
@en
Mohamed A. Elmonem
@es
type
label
Mohamed A Elmonem
@nl
Mohamed A Elmonem
@sl
Mohamed A. Elmonem
@en
Mohamed A. Elmonem
@es
prefLabel
Mohamed A Elmonem
@nl
Mohamed A Elmonem
@sl
Mohamed A. Elmonem
@en
Mohamed A. Elmonem
@es
P1053
G-2939-2017
P106
P1153
55921282400
P21
P31
P3829
P496
0000-0002-3154-1948