Mohammad S. Haggar-Al

El Gomhouria Street
Al Mansurah, DK 35516, Egypt

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 22 publications

Evaluation of FABP1 as a biomarker of diabetic kidney disease in children with type 1 diabetes.

Evaluation of FABP1 as a biomarker of diabetic kidney disease in children with type 1 diabetes.

Journal: European journal of pediatrics

Published: November 30, 2025

Clinical, phenotype and genotype correlations in primary ciliary dyskinesia suspected children in Egypt.

Clinical, phenotype and genotype correlations in primary ciliary dyskinesia suspected children in Egypt.

Journal: Frontiers in molecular biosciences

Published: June 05, 2025

Modified National Early Warning Score 2, warning system for predicting treatment outcomes in patients with emphysematous pyelonephritis.

Modified National Early Warning Score 2, warning system for predicting treatment outcomes in patients with emphysematous pyelonephritis.

Journal: World journal of nephrology

Published: April 02, 2025

Biallelic Variants in MNS1 Are Associated with Laterality Defects and Respiratory Involvement.

Biallelic Variants in MNS1 Are Associated with Laterality Defects and Respiratory Involvement.

Journal: Cells

Published: April 30, 2024

Clinical manifestations in Egyptian Pompe disease patients: Molecular variability and enzyme replacement therapy (ERT) outcomes.

Clinical manifestations in Egyptian Pompe disease patients: Molecular variability and enzyme replacement therapy (ERT) outcomes.

Journal: Italian journal of pediatrics

Published: March 07, 2024

Tricuspid mass-curious case of Li-Fraumeni syndrome: A letter to the editor.

Tricuspid mass-curious case of Li-Fraumeni syndrome: A letter to the editor.

Journal: World journal of clinical cases

Published: March 06, 2024

Retraction Note: Endothelin-1 and Leptin as Markers of Intrauterine Growth Restriction.

Retraction Note: Endothelin-1 and Leptin as Markers of Intrauterine Growth Restriction.

Journal: Indian journal of pediatrics

Published: February 29, 2024

Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children.

Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children.

Journal: Molecular biology reports

Published: January 03, 2023

Recurrence pattern of non-syndromic familial congenital heart diseases among a large cohort of families from Egypt.

Recurrence pattern of non-syndromic familial congenital heart diseases among a large cohort of families from Egypt.

Journal: BMC pediatrics

Published: April 21, 2022

Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma.

Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma.

Journal: Journal of pediatric genetics

Published: September 15, 2019

A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis.

A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis.

Journal: Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

Published: January 18, 2017

Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt.

Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt.

Journal: Indian journal of human genetics

Published: June 25, 2014

Showing 1-12 of 22

Last Updated: 09/26/2026