Hazem S. Awad
Dubai, DU, United Arab Emirates
Last Updated: 09/26/2026
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Found 14 publications
RETICULOCYTE SUBPOPULATION ANALYSIS AND ITS CORRELATION WITH IRON DEFICIENCY ANEMIA: A RETROSPECTIVE STUDY IN A PREDOMINANTLY FEMALE POPULATION.
Journal: Georgian medical news
Published: May 02, 2026
Isolated Kidney Transplant in Primary Hyperoxaluria-1 Enabled by Small Interfering RNA (siRNA) Therapy. Is It Time for Change? Case Report and Review of the Literature.
Journal: Pediatric transplantation
Published: September 11, 2025
Early-Start Versus Late-Start Icodextrin for Children Receiving Chronic Peritoneal Dialysis: Findings from the International Pediatric Peritoneal Dialysis Network.
Journal: Clinical journal of the American Society of Nephrology : CJASN
Published: April 13, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 08, 2024
Prospective Study of Modifiable Risk Factors of Arterial Hypertension and Left Ventricular Hypertrophy in Pediatric Patients on Hemodialysis.
Journal: Kidney international reports
Published: February 17, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions.
Journal: Genes & diseases
Published: March 14, 2023
Relapsing and refractory peritoneal dialysis peritonitis caused by Corynebacterium amycolatum.
Journal: Pediatric nephrology (Berlin, Germany)
Published: September 16, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Journal: European urology open science
Published: August 10, 2022
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.
Journal: American journal of medical genetics. Part A
Published: October 27, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 08, 2021
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Journal: American journal of medical genetics. Part A
Published: April 30, 2021
Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome.
Journal: Kidney international reports
Published: September 05, 2020
Last Updated: 09/26/2026