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Mohamed Shaheed

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Jeroen van Reeuwijk; Prabhjit K Grewal; Mustafa A Salih; Daniel Beltrán-Valero de Bernabé; Jenny M McLaughlan; Caroline B Michielse; Ralf Herrmann; Jane E Hewitt; Alice Steinbrecher; Mohamed Z Seidahmed; Mohamed M Shaheed; Abdullah M Abomelha; Han G Brunner; Hans van Bokhoven; Thomas Voit
Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.
Mohamed Z Seidahmed; Mohamed M Shaheed; Omar B Abdulbasit; Hessa Al Dohami; Mirghani Babiker; Mohammed A Abdullah; Abdullah M Abomelha
A case of methotrexate embryopathy with holoprosencephaly, expanding the phenotype.
Mohamed Z Seidahmed; E A Alyamani; Mohamed S Rashed; Amal A A Saadallah; OB Abdelbasit; Mohamed M Shaheed; A Rasheed; F A Hamid; M A Sabry
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.

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2007: Jeroen van Reeuwijk; Prabhjit K Grewal; Mustafa A Salih; Daniel Beltrán-Valero de Bernabé; Jenny M McLaughlan; Caroline B Michielse; Ralf Herrmann; Jane E Hewitt; Alice Steinbrecher; Mohamed Z Seidahmed; Mohamed M Shaheed; Abdullah M Abomelha; Han G Brunner; Hans van Bokhoven; Thomas Voit
Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.
Human genetics 2007;121(6):685-90.
2006: Mohamed Z Seidahmed; Mohamed M Shaheed; Omar B Abdulbasit; Hessa Al Dohami; Mirghani Babiker; Mohammed A Abdullah; Abdullah M Abomelha
A case of methotrexate embryopathy with holoprosencephaly, expanding the phenotype.
Birth defects research. Part A, Clinical and molecular teratology 2006;76(2):138-42.
2005: Mohamed Z Seidahmed; E A Alyamani; Mohamed S Rashed; Amal A A Saadallah; OB Abdelbasit; Mohamed M Shaheed; A Rasheed; F A Hamid; M A Sabry
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
American journal of medical genetics. Part A 2005;136(2):205-9.
2004: A M Miqdad; OB Abdelbasit; Mohamed M Shaheed; Mohamed Z Seidahmed; Abdullah M Abomelha; O P Arcala
Intravenous immunoglobulin G (IVIG) therapy for significant hyperbilirubinemia in ABO hemolytic disease of the newborn.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2004;16(3):163-6.
2000: OB Abdelbasit; Mohamed M Shaheed; M S Al-Omari; Abdullah M Abomelha; M O Babiker
Gastric perforation. An unusual cause of ascites in a newborn baby.
Saudi medical journal 2000;21(11):1085-7.
1999: Mohamed Z Seidahmed; D E Rooney; Mustafa A Salih; O B Basit; Mohamed M Shaheed; Mohammed A Abdullah; Abdullah M Abomelha
Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome.
American journal of medical genetics 1999;85(2):185-8.