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British Medical Journal (Clinical Research Ed.)
|
July 30, 1983
Wilson's disease: a diagnostic dilemma
H Nazer, V F Larcher, R J Ede, et al.
Clinical Genetics
|
May 1, 1996
Severe dental aberrations in familial steroid dehydrogenase deficiency: a new association
S P Lyngstadaas, C J Crossner, H Nazer, et al.
The Canadian Journal of Hospital Pharmacy
|
June 12, 2025
An Innovative Approach to Interdisciplinary Training: A Pharmacy Resident's Day with a Critical Care Nurse
Lama H Nazer, Naheel Said, Wedad Awad, et al.
BMC Infectious Diseases
|
August 10, 2018
Fixed-dose combination associated with faster time to smear conversion compared to separate tablets of anti-tuberculosis drugs in patients with poorly controlled diabetes and pulmonary tuberculosis in Qatar
Mohammad H Al-Shaer, Hazem Elewa, Yosra Alkabab, et al.
Neuroradiology
|
January 1, 1993
Magnetic resonance imaging of the brain in Wilson's disease
H Nazer, J Brismar, M Z al-Kawi, et al.
Clinical Genetics
|
November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology
V A Coronado, J A Bonneville, H Nazer, et al.
European Journal of Pediatrics
|
January 1, 1989
Cystic fibrosis in Saudi Arabia
H Nazer, E Riff, N Sakati, et al.
Journal of Lipid Research
|
May 1, 1991
Bile acids and bile alcohols in a child with hepatic 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency: effects of chenodeoxycholic acid treatment
H Ichimiya, B Egestad, H Nazer, et al.
European Journal of Pediatrics
|
June 2, 2000
Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations
M Kambouris, H Banjar, I Moggari, et al.
The Journal of Clinical Investigation
|
November 9, 2000
The bile acid synthetic gene 3beta-hydroxy-Delta(5)-C(27)-steroid oxidoreductase is mutated in progressive intrahepatic cholestasis
M Schwarz, A C Wright, D L Davis, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 103) with videos related to
Sort By:
Page
of 11
British Medical Journal (Clinical Research Ed.)
|
July 30, 1983
Wilson's disease: a diagnostic dilemma
H Nazer, V F Larcher, R J Ede, et al.
Clinical Genetics
|
May 1, 1996
Severe dental aberrations in familial steroid dehydrogenase deficiency: a new association
S P Lyngstadaas, C J Crossner, H Nazer, et al.
The Canadian Journal of Hospital Pharmacy
|
June 12, 2025
An Innovative Approach to Interdisciplinary Training: A Pharmacy Resident's Day with a Critical Care Nurse
Lama H Nazer, Naheel Said, Wedad Awad, et al.
BMC Infectious Diseases
|
August 10, 2018
Fixed-dose combination associated with faster time to smear conversion compared to separate tablets of anti-tuberculosis drugs in patients with poorly controlled diabetes and pulmonary tuberculosis in Qatar
Mohammad H Al-Shaer, Hazem Elewa, Yosra Alkabab, et al.
Neuroradiology
|
January 1, 1993
Magnetic resonance imaging of the brain in Wilson's disease
H Nazer, J Brismar, M Z al-Kawi, et al.
Clinical Genetics
|
November 15, 2005
COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology
V A Coronado, J A Bonneville, H Nazer, et al.
European Journal of Pediatrics
|
January 1, 1989
Cystic fibrosis in Saudi Arabia
H Nazer, E Riff, N Sakati, et al.
Journal of Lipid Research
|
May 1, 1991
Bile acids and bile alcohols in a child with hepatic 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency: effects of chenodeoxycholic acid treatment
H Ichimiya, B Egestad, H Nazer, et al.
European Journal of Pediatrics
|
June 2, 2000
Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations
M Kambouris, H Banjar, I Moggari, et al.
The Journal of Clinical Investigation
|
November 9, 2000
The bile acid synthetic gene 3beta-hydroxy-Delta(5)-C(27)-steroid oxidoreductase is mutated in progressive intrahepatic cholestasis
M Schwarz, A C Wright, D L Davis, et al.
Page
of 11