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

por Rakha, Shaimaa, Mohy-Eldeen, Rehab, Al-Haggar, Mohammad, El-Bayoumi, Mohammed Attia
Publicado 2022

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

por al-azzawy, Mohammed F., Al-Haggar, Mohammad, ElSaid, Afaf M., El-khawaga, Omali Y.
Publicado 2023

Fanconi Bickel Syndrome: Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families

por Al-Haggar, Mohammad, Sakamoto, Osamu, Shaltout, Ali, El-Hawary, Amany, Wahba, Yahya, Abdel-Hadi, Dina
Publicado 2011

Vitamin E and N-Acetylcysteine as Antioxidant Adjuvant Therapy in Children with Acute Lymphoblastic Leukemia

por Al-Tonbary, Youssef, Al-Haggar, Mohammad, EL-Ashry, Rasha, EL-Dakroory, Sahar, Azzam, Hanan, Fouda, Ashraf
Publicado 2009

Disruptive behavior in Down syndrome children: a cross-sectional comparative study

por Yahia, Sohier, El-Hadidy, Mohamed, El-Gilany, Abdel-Hady, Amdel-Hady, Dina, Wahba, Yahya, Al-Haggar, Mohammad
Publicado 2014

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

por Al-Haggar, Mohammad S., Yahia, Sohier, Abdel-Hady, Dina, Al-Saied, Afaf, Al-Kenawy, Rasha, Abo-El-Kasem, Rabab
Publicado 2014

Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature

por Al-Haggar, Mohammad, Ahmad, Nermin, Yahia, Sohier, Shams, Amany, Hasaneen, Bothina, Hassan Hassan, Rasha, Wahba, Yahya, Salem, Nanees Abdel-Badie, Abdel-Hady, Dina
Publicado 2013