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Genomics
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November 4, 1998
The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation
O Chiba-Falek, E Kerem, T Shoshani, et al.
Lancet (London, England)
|
November 26, 1994
Congenital bilateral absence of vas deferens in the absence of cystic fibrosis
A Augarten, Y Yahav, B S Kerem, et al.
Lancet (London, England)
|
July 3, 1993
Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation
A Augarten, B S Kerem, Y Yahav, et al.
American Journal of Human Genetics
|
January 1, 1997
The molecular basis of partial penetrance of splicing mutations in cystic fibrosis
N Rave-Harel, E Kerem, M Nissim-Rafinia, et al.
Pediatric Pulmonology
|
November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patients
A Barak, I D Wexler, O Efrati, et al.
Clinical and Experimental Medicine
|
January 28, 2005
Systemic inflammatory mediators and cystic fibrosis genotype
A Augarten, G Paret, I Avneri, et al.
Pediatrics
|
January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver disease
M Wilschanski, J Rivlin, S Cohen, et al.
Paediatric Anaesthesia
|
May 22, 2001
Soluble P-selectin and the postoperative course following cardiopulmonary bypass in children
D Lotan, T Prince, O Dagan, et al.
Pediatrics
|
April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype
E Kerem, M Nissim-Rafinia, Z Argaman, et al.
International Journal of Clinical & Laboratory Research
|
January 8, 1999
Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosis
A Augarten, D Katznelson, L Dubenbaum, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Genomics
|
November 4, 1998
The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation
O Chiba-Falek, E Kerem, T Shoshani, et al.
Lancet (London, England)
|
November 26, 1994
Congenital bilateral absence of vas deferens in the absence of cystic fibrosis
A Augarten, Y Yahav, B S Kerem, et al.
Lancet (London, England)
|
July 3, 1993
Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation
A Augarten, B S Kerem, Y Yahav, et al.
American Journal of Human Genetics
|
January 1, 1997
The molecular basis of partial penetrance of splicing mutations in cystic fibrosis
N Rave-Harel, E Kerem, M Nissim-Rafinia, et al.
Pediatric Pulmonology
|
November 9, 2004
Trampoline use as physiotherapy for cystic fibrosis patients
A Barak, I D Wexler, O Efrati, et al.
Clinical and Experimental Medicine
|
January 28, 2005
Systemic inflammatory mediators and cystic fibrosis genotype
A Augarten, G Paret, I Avneri, et al.
Pediatrics
|
January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver disease
M Wilschanski, J Rivlin, S Cohen, et al.
Paediatric Anaesthesia
|
May 22, 2001
Soluble P-selectin and the postoperative course following cardiopulmonary bypass in children
D Lotan, T Prince, O Dagan, et al.
Pediatrics
|
April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype
E Kerem, M Nissim-Rafinia, Z Argaman, et al.
International Journal of Clinical & Laboratory Research
|
January 8, 1999
Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosis
A Augarten, D Katznelson, L Dubenbaum, et al.
Page
of 5