Mohammad Al-Haggar
Mohammad Al-Haggar
Professor of Pediatrics, Chief of Genetics Unit, Mansoura University, Egypt
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Endothelin-1 and leptin as markers of intrauterine growth restriction
MAS Nezar, AMA El-Baky, OAS Soliman, HAS Abdel-Hady, AM Hammad, ...
The Indian Journal of Pediatrics 76 (5), 485-488, 2009
Vitamin e and N-acetylcysteine as antioxidant adjuvant therapy in children with acute lymphoblastic leukemia
Y Al-Tonbary, M Al-Haggar, R El-Ashry, S El-Dakroory, H Azzam, A Fouda
Advances in Hematology 2009, 2009
Biofeedback and cognitive behavioral therapy for Egyptian adolescents suffering from chronic fatigue syndrome
MS Al-Haggar, ZA Al-Naggar, MA Abdel-Salam
Journal of pediatric neurology 4 (03), 161-169, 2006
A novel homozygous p. Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome
M Al-Haggar, A Madej-Pilarczyk, L Kozlowski, JM Bujnicki, S Yahia, ...
European journal of human genetics 20 (11), 1134-1140, 2012
Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats
HIH El-Sayyad, MMS Al-Haggar, HA El-Ghawet, IHM Bakr
Nutrition 30 (3), 326-336, 2014
Sirenomelia (symelia apus) with Potter's syndrome in connection with gestational diabetes mellitus: a case report and literature review
M Al-Haggar, S Yahia, D Abdel-Hadi, F Grill, A Al Kaissi
African health sciences 10 (4), 2010
Impact of long-term oral iron supplementation in breast-fed infants
N Abdelrazik, M Al-Haggar, H Al-Marsafawy, H Abdel-Hadi, R Al-Baz, ...
The Indian Journal of Pediatrics 74 (8), 739-745, 2007
Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations
M Al-Haggar
World journal of nephrology 2 (4), 94, 2013
Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia
A Settin, M Al Haggar, T Al Dosoky, R Al Baz, NM Abdelrazik, M Fouda, ...
The Indian Journal of Pediatrics 74 (3), 255-263, 2007
Screening for G6PD Mediterranean mutation among Egyptian neonates with high or prolonged jaundice
A Settin, M Al-Haggar, R Al-Baz, H Yousof, N Osman
Haema 9 (1), 83-90, 2006
Bioinformatics in high throughput sequencing: application in evolving genetic diseases
MM Al-Haggar, BA Khair-Allaha, MM Islam, ASA Mohamed
J Data Mining Genomics Proteomics 4 (131), 2153-0602.1000131, 2013
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family
M Al-Haggar, A Bakr, T Tajima, K Fujieda, A Hammad, O Soliman, ...
Clinical and experimental nephrology 13 (4), 288-294, 2009
p. R672C mutation of MYH3 gene in an Egyptian infant presented with Freeman-Sheldon syndrome
M Al-Haggar, S Yahia, K Damjanovich, N Ahmad, I Hamada, ...
The Indian Journal of Pediatrics 78 (1), 103-105, 2011
Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia: cases from Mansoura, Egypt
A Settin, M Al Haggar, T Al Dosok, R Al Baz, N Abdelrazik, M Fouda, ...
Hematology 11 (5-6), 341-349, 2006
Disruptive behavior in Down syndrome children: a cross-sectional comparative study
S Yahia, M El-Hadidy, AH El-Gilany, D Amdel-Hady, Y Wahba, ...
Annals of Saudi medicine 34 (6), 517-521, 2014
Fanconi Bickel syndrome: novel mutations in GLUT 2 gene causing a distinguished form of renal tubular acidosis in two unrelated Egyptian families
M Al-Haggar, O Sakamoto, A Shaltout, A El-Hawary, Y Wahba, ...
Case Reports in Nephrology 2011, 2011
Single nucleotide polymorphism of IL4C-590T and IL4RA 175V and immunological parameters in Egyptian asthmatics with different clinical phenotypes
M Zedan, A Bakr, B Shouman, H Zaghloul, M Al-Haggar, M Zedan, ...
J Allergy Ther 5 (189), 2, 2014
Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome
M Al‐Haggar, N Salem, Y Wahba, N Ahmad, L Jonard, D Abdel‐Hady, ...
Pediatric Diabetes 16 (4), 305-316, 2015
Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children’Hospital, Mansoura, Egypt
MS Al-Haggar, S Yahia, D Abdel-Hady, A Al-Saied, R Al-Kenawy, ...
Indian Journal of Human Genetics 20 (1), 43, 2014
Sporadic fibrodysplasia ossificans progressiva in an Egyptian infant with c. 617G> A mutation in ACVR1 gene: a case report and review of literature
M Al-Haggar, N Ahmad, S Yahia, A Shams, B Hasaneen, ...
Case Reports in Genetics 2013, 2013
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