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Mohamed Al-Hamed

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Cystic Fibrosis Transmembrane Conductance Regulator

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Hussein Raef; Minjing Zou; Nada N Abu-Dheim; Mohammed H Al-Ghamdi; Mohamed Al-Hamed; Hindi Al-Hindi; Roua A Al-Rijjal; Essa Baitei; Namik Kaya; Brian F Meyer; Dorota Monies; Yufei Shi
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.
Saeed Bohlega; G Van Goethem; Abdulaziz Al-Semari; A Löfgren; Mohamed Al-Hamed; Christine Van Broeckhoven; Marios Kambouris
Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failure.
Ghazi Alsbeih; Najla Al-Harbi; Muneera Al-Buhairi; K Al-Hadyan; Mohamed Al-Hamed
Association between TP53 codon 72 single-nucleotide polymorphism and radiation sensitivity of human fibroblasts.

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All Publications

2011: Hussein Raef; Minjing Zou; Nada N Abu-Dheim; Mohammed H Al-Ghamdi; Mohamed Al-Hamed; Hindi Al-Hindi; Roua A Al-Rijjal; Essa Baitei; Namik Kaya; Brian F Meyer; Dorota Monies; Yufei Shi
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.
Clinical endocrinology 2011;75(6):791-800.
2009: Saeed Bohlega; G Van Goethem; Abdulaziz Al-Semari; A Löfgren; Mohamed Al-Hamed; Christine Van Broeckhoven; Marios Kambouris
Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failure.
Neuromuscular disorders : NMD 2009;19(12):845-8.
2007: Ghazi Alsbeih; Najla Al-Harbi; Muneera Al-Buhairi; K Al-Hadyan; Mohamed Al-Hamed
Association between TP53 codon 72 single-nucleotide polymorphism and radiation sensitivity of human fibroblasts.
Radiation research 2007;167(5):535-40.
2006: Pamela Carroll; Hamad Al-Mojalli; ABBAS ALABBAD; Ibrahim Al-Hassoun; Mohamed Al-Hamed; Rana Al-Amr; BUTT ABDUL; Brian F Meyer
Novel mutations underlying nephrogenic diabetes insipidus in Arab families.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(7):443-7.
2006: Osama Alsmadi; Fadi Alkayal; Mohamed Al-Hamed; Brian F Meyer
Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study.
BMC medical genetics 2006;7():43.
2004: A Abdul Wahab; G al Thani; ST Dawod; Marios Kambouris; Mohamed Al-Hamed
Rare CFTR mutation 1525-1G>A in a Pakistani patient.
Journal of tropical pediatrics 2004;50(2):120-2.
2002: A Abdul Wahab; Ibrahim A Janahi; S Hebi; Mohamed Al-Hamed; Marios Kambouris
Cystic fibrosis in a child from Syria.
Annals of tropical paediatrics 2002;22(1):53-5.
2001: Atiqa Abdul-Wahab; G al Thani; ST Dawod; Marios Kambouris; Mohamed Al-Hamed
Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V).
Journal of tropical pediatrics 2001;47(2):110-2.
2000: Marios Kambouris; Hanaa H Banjar; I Moggari; H Nazer; Mohamed Al-Hamed; Brian F Meyer
Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations.
European journal of pediatrics 2000;159(5):303-9.
1999: Emtethal Al-Jishi; Brian F Meyer; Mohamed S Rashed; Mazen Al-Essa; Mohamed Al-Hamed; Nadia A Sakati; Sami A Sanjad; Pinar T Ozand; Marios Kambouris
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.
Clinical genetics 1999;55(6):444-9.