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H H Seydewitz

Showing results (11-20 of 21) with videos related to

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The Journal of Pediatrics|November 1, 1996
Primary treatment of propionic acidemia complicated by acute thiamine deficiencyD Matern, H H Seydewitz, W Lehnert, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|April 14, 2000
Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patientsM Mall, A Wissner, H H Seydewitz, et al.
Pediatric Pulmonology|May 7, 1999
Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotypeS Beck, J Kühr, V V Schütz, et al.
The European Respiratory Journal|November 26, 1999
Upper airway inflammation in children exposed to ambient ozone and potential signs of adaptationM V Kopp, C Ulmer, G Ihorst, et al.
British Journal of Pharmacology|August 22, 2000
Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytesM Mall, A Wissner, H H Seydewitz, et al.
The American Journal of Physiology|December 9, 1998
Cholinergic ion secretion in human colon requires coactivation by cAMPM Mall, M Bleich, M Schürlein, et al.
American Journal of Respiratory Cell and Molecular Biology|September 6, 2000
Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epitheliaM Mall, A Wissner, R Schreiber, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 16, 1999
Circadian variation of urinary eosinophil protein X in asthmatic and healthy childrenK Storm van's Gravesande, J Mattes, T Grüntjens, et al.
Pediatric Research|August 29, 2000
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotypeB W Weston, J L Lin, J Muenzer, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Pediatrics|November 1, 1996
Primary treatment of propionic acidemia complicated by acute thiamine deficiencyD Matern, H H Seydewitz, W Lehnert, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|April 14, 2000
Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patientsM Mall, A Wissner, H H Seydewitz, et al.
Pediatric Pulmonology|May 7, 1999
Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotypeS Beck, J Kühr, V V Schütz, et al.
The European Respiratory Journal|November 26, 1999
Upper airway inflammation in children exposed to ambient ozone and potential signs of adaptationM V Kopp, C Ulmer, G Ihorst, et al.
British Journal of Pharmacology|August 22, 2000
Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytesM Mall, A Wissner, H H Seydewitz, et al.
The American Journal of Physiology|December 9, 1998
Cholinergic ion secretion in human colon requires coactivation by cAMPM Mall, M Bleich, M Schürlein, et al.
American Journal of Respiratory Cell and Molecular Biology|September 6, 2000
Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epitheliaM Mall, A Wissner, R Schreiber, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 16, 1999
Circadian variation of urinary eosinophil protein X in asthmatic and healthy childrenK Storm van's Gravesande, J Mattes, T Grüntjens, et al.
Pediatric Research|August 29, 2000
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotypeB W Weston, J L Lin, J Muenzer, et al.
Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.
Pageof 3