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American Journal of Medical Genetics
|
January 1, 1992
Alagille syndrome with de novo del(20) (p11.2)
A S Teebi, D S Murthy, E A Ismail, et al.
Analytical Biochemistry
|
April 9, 2020
Reversible associations between human plasma fibronectin and fibrinogen γγ' heterodimer observed by high pressure size exclusion chromatography and dynamic light scattering
Frank M Fabian, Ayman E A Ismail, Ou Wang, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 1, 1997
Genotypic/phenotypic heterogeneity of selective vitamin B12 malabsorption (Grasbeck-Imerslund syndrome) in two Bedouin families
E A Ismail, Q Al Saleh, M A Sabry, et al.
European Journal of Pediatrics
|
September 1, 1996
The association of cystic fibrosis with homocystinura in two Saudi siblings
E A Ismail, Q A al Saleh, M Zaki, et al.
Virchows Archiv : an International Journal of Pathology
|
January 1, 1994
Indian childhood cirrhosis--like liver disease in an Arab child. A brief report
I A Aljajeh, S Mughal, B al-Tahou, et al.
Andrology
|
June 29, 2019
Early administration of phosphodiesterase 5 inhibitors after induction of diabetes in a rat model may prevent erectile dysfunction
E A Ismail, S E Younis, I Y Ismail, et al.
Annals of Tropical Paediatrics
|
December 22, 1999
Persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis): a report from Kuwait
D G Ramadan, M H Badawi, M Zaki, et al.
Journal of Child Neurology
|
October 31, 1998
An epidemiologic, clinical, and therapeutic study of childhood Guillain-Barré syndrome in Kuwait: is it related to the oral polio vaccine?
E A Ismail, I S Shabani, M Badawi, et al.
Journal of Medical Genetics
|
October 10, 1997
Unusual traits associated with Robinow syndrome
M A Sabry, E A Ismail, R L al-Naggar, et al.
Human Mutation
|
October 23, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency
Y Indo, S Mardy, Y Miura, et al.
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of 3
Search research articles
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Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
January 1, 1992
Alagille syndrome with de novo del(20) (p11.2)
A S Teebi, D S Murthy, E A Ismail, et al.
Analytical Biochemistry
|
April 9, 2020
Reversible associations between human plasma fibronectin and fibrinogen γγ' heterodimer observed by high pressure size exclusion chromatography and dynamic light scattering
Frank M Fabian, Ayman E A Ismail, Ou Wang, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 1, 1997
Genotypic/phenotypic heterogeneity of selective vitamin B12 malabsorption (Grasbeck-Imerslund syndrome) in two Bedouin families
E A Ismail, Q Al Saleh, M A Sabry, et al.
European Journal of Pediatrics
|
September 1, 1996
The association of cystic fibrosis with homocystinura in two Saudi siblings
E A Ismail, Q A al Saleh, M Zaki, et al.
Virchows Archiv : an International Journal of Pathology
|
January 1, 1994
Indian childhood cirrhosis--like liver disease in an Arab child. A brief report
I A Aljajeh, S Mughal, B al-Tahou, et al.
Andrology
|
June 29, 2019
Early administration of phosphodiesterase 5 inhibitors after induction of diabetes in a rat model may prevent erectile dysfunction
E A Ismail, S E Younis, I Y Ismail, et al.
Annals of Tropical Paediatrics
|
December 22, 1999
Persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis): a report from Kuwait
D G Ramadan, M H Badawi, M Zaki, et al.
Journal of Child Neurology
|
October 31, 1998
An epidemiologic, clinical, and therapeutic study of childhood Guillain-Barré syndrome in Kuwait: is it related to the oral polio vaccine?
E A Ismail, I S Shabani, M Badawi, et al.
Journal of Medical Genetics
|
October 10, 1997
Unusual traits associated with Robinow syndrome
M A Sabry, E A Ismail, R L al-Naggar, et al.
Human Mutation
|
October 23, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency
Y Indo, S Mardy, Y Miura, et al.
Page
of 3