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J Rivlin

Showing results (11-20 of 28) with videos related to

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European Journal of Respiratory Diseases|October 1, 1985
Long-term follow up of children with the Wilson-Mikity syndromeJ Rivlin, K Pape, B J Reilly, et al.
The American Review of Respiratory Disease|March 1, 1984
Upper airway morphology in patients with idiopathic obstructive sleep apneaJ Rivlin, V Hoffstein, J Kalbfleisch, et al.
The Journal of Pediatrics|February 21, 1998
Severe Clostridium difficile-associated colitis in young patients with cystic fibrosisJ Rivlin, A Lerner, A Augarten, et al.
American Journal of Respiratory and Critical Care Medicine|March 11, 2000
A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutationsM Wilschanski, C Famini, H Blau, et al.
The Journal of Pediatrics|May 23, 2007
Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized associationA S Luder, H Mandel, M Khayat, et al.
Journal of Children'S Orthopaedics|August 13, 2016
Spica magnetic resonance imaging for determination of abduction angle: initial results and reproducibility assessmentM J Rivlin, J H Kan, E K Schallert, et al.
Human Genetics|September 1, 1990
The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and ArabsI Lerer, S Cohen, M Chemke, et al.
The Journal of Clinical Investigation|April 1, 1994
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cellsT Shoshani, E Kerem, A Szeinberg, et al.
Journal of Pediatric Orthopedics. Part B|February 27, 2019
Spica MRI predictors for epiphyseal osteonecrosis after closed reduction treatment of dysplasia of the hipLee S Haruno, J Herman Kan, Michael J Rivlin, et al.
Human Genetics|August 1, 1995
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in IsraelE Kerem, Y M Kalman, Y Yahav, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
European Journal of Respiratory Diseases|October 1, 1985
Long-term follow up of children with the Wilson-Mikity syndromeJ Rivlin, K Pape, B J Reilly, et al.
The American Review of Respiratory Disease|March 1, 1984
Upper airway morphology in patients with idiopathic obstructive sleep apneaJ Rivlin, V Hoffstein, J Kalbfleisch, et al.
The Journal of Pediatrics|February 21, 1998
Severe Clostridium difficile-associated colitis in young patients with cystic fibrosisJ Rivlin, A Lerner, A Augarten, et al.
American Journal of Respiratory and Critical Care Medicine|March 11, 2000
A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutationsM Wilschanski, C Famini, H Blau, et al.
The Journal of Pediatrics|May 23, 2007
Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized associationA S Luder, H Mandel, M Khayat, et al.
Journal of Children'S Orthopaedics|August 13, 2016
Spica magnetic resonance imaging for determination of abduction angle: initial results and reproducibility assessmentM J Rivlin, J H Kan, E K Schallert, et al.
Human Genetics|September 1, 1990
The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and ArabsI Lerer, S Cohen, M Chemke, et al.
The Journal of Clinical Investigation|April 1, 1994
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cellsT Shoshani, E Kerem, A Szeinberg, et al.
Journal of Pediatric Orthopedics. Part B|February 27, 2019
Spica MRI predictors for epiphyseal osteonecrosis after closed reduction treatment of dysplasia of the hipLee S Haruno, J Herman Kan, Michael J Rivlin, et al.
Human Genetics|August 1, 1995
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in IsraelE Kerem, Y M Kalman, Y Yahav, et al.
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