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M Wilschanski

Showing results (11-20 of 38) with videos related to

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Gastroenterology|December 1, 1996
Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expressionD R Mack, G G Forstner, M Wilschanski, et al.
Thorax|December 31, 2005
Cystic fibrosis: terminology and diagnostic algorithmsK De Boeck, M Wilschanski, C Castellani, et al.
The Journal of Pediatrics|November 1, 1995
Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutationsM Wilschanski, J Zielenski, D Markiewicz, et al.
European Journal of Clinical Investigation|June 14, 2005
WNK4 regulates airway Na+ transport: study of familial hyperkalaemia and hypertensionZ Farfel, H Mayan, Y Yaacov, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 5, 1999
Findings on routine abdominal ultrasonography in cystic fibrosis patientsM Wilschanski, D Fisher, I Hadas-Halperin, 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.
Lancet (London, England)|June 17, 1995
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermiaK Jarvi, J Zielenski, M Wilschanski, et al.
Human Molecular Genetics|July 1, 1997
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNAR Rozmahel, K Gyömörey, S Plyte, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 5, 2000
Neonatal sclerosing cholangitis associated with autoimmune phenomenaM Bar Meir, I Hadas-Halperin, D Fisher, et al.
JAMA|August 28, 1996
Diversity of reproductive tract abnormalities in men with cystic fibrosisM Wilschanski, M Corey, P Durie, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Gastroenterology|December 1, 1996
Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expressionD R Mack, G G Forstner, M Wilschanski, et al.
Thorax|December 31, 2005
Cystic fibrosis: terminology and diagnostic algorithmsK De Boeck, M Wilschanski, C Castellani, et al.
The Journal of Pediatrics|November 1, 1995
Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutationsM Wilschanski, J Zielenski, D Markiewicz, et al.
European Journal of Clinical Investigation|June 14, 2005
WNK4 regulates airway Na+ transport: study of familial hyperkalaemia and hypertensionZ Farfel, H Mayan, Y Yaacov, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 5, 1999
Findings on routine abdominal ultrasonography in cystic fibrosis patientsM Wilschanski, D Fisher, I Hadas-Halperin, 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.
Lancet (London, England)|June 17, 1995
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermiaK Jarvi, J Zielenski, M Wilschanski, et al.
Human Molecular Genetics|July 1, 1997
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNAR Rozmahel, K Gyömörey, S Plyte, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 5, 2000
Neonatal sclerosing cholangitis associated with autoimmune phenomenaM Bar Meir, I Hadas-Halperin, D Fisher, et al.
JAMA|August 28, 1996
Diversity of reproductive tract abnormalities in men with cystic fibrosisM Wilschanski, M Corey, P Durie, et al.
Pageof 4