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Works by Abdel-Hadi, Dina

Results: 3

1

A Novel Fibrillin–1 Mutation in an Egyptian Marfan Family: A Proband Showing Nephrotic Syndrome Due to Focal Segmental Glomerulosclerosis.

Published in:

Saudi Journal of Kidney Diseases & Transplantation, 2017, v. 28, n. 1, p. 141, doi. 10.4103/1319-2442.198166

By:

Al-Haggar, Mohammad;
Bakr, Ashraf;
Wahba, Yahya;
Coucke, Paul J.;
El-Hussini, Fatma;
Hafez, Mona;
Eid, Riham;
Eid, Abdel-Rahman;
Sarhan, Amr;
Shaltout, Ali;
Hammad, Ayman;
Yahia, Sohier;
El-Rifaie, Ahmad;
Abdel-Hadi, Dina

Publication type:

Article

2

Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.

Published in:

Clinical & Experimental Nephrology, 2012, v. 16, n. 4, p. 604, doi. 10.1007/s10157-012-0603-9

By:

Al-Haggar, Mohammad;
Sakamoto, Osamu;
Shaltout, Ali;
Al-Hawari, Amani;
Wahba, Yahya;
Abdel-Hadi, Dina

Publication type:

Article

3

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

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1134, doi. 10.1038/ejhg.2012.77

By:

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

Publication type:

Article