Fanconi-Bickel syndrome as an example of marked allelic heterogeneity

Por Al-Haggar, Mohammad
Publicado em 2012

Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations

Por Al-Haggar, Mohammad
Publicado em 2013

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 em 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 em 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 no Ann Saudi Med (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 em 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 em 2013

A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome

Por Al-Haggar, Mohammad, Madej-Pilarczyk, Agnieszka, Kozlowski, Lukasz, Bujnicki, Janusz M, Yahia, Sohier, Abdel-Hadi, Dina, Shams, Amany, Ahmad, Nermin, Hamed, Sahar, Puzianowska-Kuznicka, Monika
Publicado em 2012