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Cancer Letters
|
February 13, 2001
Antioxidants enhance the susceptibility of colon carcinoma cells to 5-fluorouracil by augmenting the induction of the bax protein
D Adeyemo, F Imtiaz, S Toffa, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria
M Al-Sayed, S Alahmed, O Alsmadi, et al.
Journal of Inherited Metabolic Disease
|
May 9, 2000
Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1
F Imtiaz, V Worthington, M Champion, et al.
Journal of Medical Genetics
|
October 4, 2007
The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population
F Imtiaz, E Savilahti, A Sarnesto, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2014
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings
O Khalifa, F Imtiaz, K Ramzan, et al.
Archives of Disease in Childhood
|
September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose
C J Hendriksz, P McClean, M J Henderson, et al.
Human Mutation
|
November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)
G Matthijs, E Schollen, C Bjursell, et al.
Human Mutation
|
September 12, 2000
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)
E Schollen, L Dorland, T J de Koning, et al.
Clinical Genetics
|
June 24, 2011
Smith-Lemli-Opitz syndrome among Arabs
M Al-Owain, F Imtiaz, T Shuaib, et al.
European Journal of Neurology
|
September 12, 2019
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination
V Chelban, M Alsagob, K Kloth, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Cancer Letters
|
February 13, 2001
Antioxidants enhance the susceptibility of colon carcinoma cells to 5-fluorouracil by augmenting the induction of the bax protein
D Adeyemo, F Imtiaz, S Toffa, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria
M Al-Sayed, S Alahmed, O Alsmadi, et al.
Journal of Inherited Metabolic Disease
|
May 9, 2000
Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1
F Imtiaz, V Worthington, M Champion, et al.
Journal of Medical Genetics
|
October 4, 2007
The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population
F Imtiaz, E Savilahti, A Sarnesto, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2014
Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings
O Khalifa, F Imtiaz, K Ramzan, et al.
Archives of Disease in Childhood
|
September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose
C J Hendriksz, P McClean, M J Henderson, et al.
Human Mutation
|
November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)
G Matthijs, E Schollen, C Bjursell, et al.
Human Mutation
|
September 12, 2000
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)
E Schollen, L Dorland, T J de Koning, et al.
Clinical Genetics
|
June 24, 2011
Smith-Lemli-Opitz syndrome among Arabs
M Al-Owain, F Imtiaz, T Shuaib, et al.
European Journal of Neurology
|
September 12, 2019
Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination
V Chelban, M Alsagob, K Kloth, et al.
Page
of 1