Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
Shaheen, R, Al-Dirbashi, OY, Al-Hassnan, ZN, Al-Owain, M, Makhsheed, N, Basheeri, F, Seidahmed, MZ, Salih, MAM, Faqih, E, Zaidan, H, Al-Sayed, M, Rahbeeni, Z, Al-Sheddi, T, Hashem, M, Kurdi, W, Shimozawa, N, Alkuraya, FS
Published in Clinical genetics (01.01.2011)
Published in Clinical genetics (01.01.2011)
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Journal Article
Identification and functional consequences of a novel MRE11 mutation affecting 10 Saudi Arabian patients with the ataxia telangiectasia-like disorder
Fernet, Marie, Gribaa, Moez, Salih, Mustafa A.M., Seidahmed, Mohamed Zein, Hall, Janet, Koenig, Michel
Published in Human molecular genetics (15.01.2005)
Published in Human molecular genetics (15.01.2005)
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Journal Article
Intravenous immunoglobulin G (IVIG) therapy for significant hyperbilirubinemia in ABO hemolytic disease of the newborn
Miqdad, AM, Abdelbasit, OB, Shaheed, MM, Seidahmed, MZ, Abomelha, AM, Arcala, OP
Published in The journal of maternal-fetal & neonatal medicine (01.09.2004)
Published in The journal of maternal-fetal & neonatal medicine (01.09.2004)
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Journal Article
Brain stem and cerebellar findings in Joubert syndrome
Alorainy, Ibrahim A, Sabir, Sohail, Seidahmed, Mohammed Z, Farooqu, Hamid A, Salih, Mustafa A
Published in Journal of computer assisted tomography (01.01.2006)
Published in Journal of computer assisted tomography (01.01.2006)
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Journal Article
A case of methotrexate embryopathy with holoprosencephaly, expanding the phenotype
Seidahmed, Mohammed Zain, Shaheed, Meeralebbae M, Abdulbasit, Omar B, Al Dohami, Hessa, Babiker, Mirghani, Abdullah, Mohammed A, Abomelha, Abdullah M
Published in Birth defects research. A Clinical and molecular teratology (01.02.2006)
Published in Birth defects research. A Clinical and molecular teratology (01.02.2006)
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Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry
Rashed, Mohamed S., Saadallah, Amal A. A., Rahbeeni, Zuhair, Eyaid, Wafaa, Seidahmed, Mohamed Z., Al-Shahwan, Saad, Salih, Mustafa A. M., Osman, Mohammad E., Al-Amoudi, Mohamed, Al-Ahaidib, Lujane, Jacob, Minnie
Published in Biomedical chromatography (01.04.2005)
Published in Biomedical chromatography (01.04.2005)
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Journal Article
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency
Seidahmed, M.Z., Alyamani, E.A., Rashed, M.S., Saadallah, A.A., Abdelbasit, O.B., Shaheed, M.M., Rasheed, A., Hamid, F.A., Sabry, M.A.
Published in American journal of medical genetics. Part A (15.07.2005)
Published in American journal of medical genetics. Part A (15.07.2005)
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Journal Article
A case of reversible cardiomyopathy & left ventricular noncompaction
Amira, Oshi, Abdelbasit, MZ, Seidahmed, K, Hussein, A, Miqdad, M, Samadi, S, Alyousef, W, Manie, M, Abdullah
Published in Journal of integrative cardiology (2016)
Published in Journal of integrative cardiology (2016)
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Journal Article
Intravenous immunoglobulin G (IVIG) therapy for significant hyperbilirubinemia in ABO hemolytic disease of the newborn
Miqdad, A M, Abdelbasit, O B, Shaheed, M M, Seidahmed, M Z, Abomelha, A M, Arcala, O P
Published in The journal of maternal-fetal & neonatal medicine (01.09.2004)
Published in The journal of maternal-fetal & neonatal medicine (01.09.2004)
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Journal Article
Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome
Seidahmed, M Z, Rooney, D E, Salih, M A, Basit, O B, Shaheed, M M, Abdullah, M A, Abomelha, A
Published in American journal of medical genetics (16.07.1999)
Published in American journal of medical genetics (16.07.1999)
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