Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S W Bender

Showing results (41-50 of 53) with videos related to

Pageof 6
Sort By:
Praxis Und Klinik Der Pneumologie|March 1, 1984
[The effect of mechanical percussion on lung function in patients with mild cystic fibrosis]R Wönne, G Plaut, H G Posselt, et al.
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1990
HLA antigen frequencies in familial Crohn's disease (CD)P Kühnl, W Sibrowski, B O Böhm, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1972
Heterozygote testing in cystic fibrosis. Metachromasia in cultured white blood cellsM Geisler, S W Bender, C Mohrmann, et al.
European Journal of Pediatrics|November 1, 1985
A double-blind placebo controlled trial with oral ambroxol and N-acetylcysteine for mucolytic treatment in cystic fibrosisF Ratjen, R Wönne, H G Posselt, et al.
Gut|December 1, 1978
Gamma heavy chain disease simulating alpha chain diseaseS W Bender, F Danon, J L Preud'homme, et al.
European Journal of Pediatrics|October 1, 1994
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorderA C Sewell, S W Bender, S Wirth, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1983
Early diagnosis of intestinal non-Hodgkin lymphoma by endoscopyJ Hintze, H G Posselt, A Walther, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 1, 1984
Biochemical quantification of crypt hyperplastic villous atrophy by aldolase activity assayS W Bender, H G Posselt, M Stäps, et al.
European Journal of Pediatrics|April 3, 1979
Evaluation of long term tobramycin therapy in patients with cystic fibrosis and advanced pulmonary diseaseU Paporisz, H G Posselt, R Wönne, et al.
Padiatrie Und Padologie|January 1, 1987
Increased concentrations of HbAlab in hereditary fructose intolerance and galactosemiaH Böhles, J Schädle, W Endres, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Praxis Und Klinik Der Pneumologie|March 1, 1984
[The effect of mechanical percussion on lung function in patients with mild cystic fibrosis]R Wönne, G Plaut, H G Posselt, et al.
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1990
HLA antigen frequencies in familial Crohn's disease (CD)P Kühnl, W Sibrowski, B O Böhm, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1972
Heterozygote testing in cystic fibrosis. Metachromasia in cultured white blood cellsM Geisler, S W Bender, C Mohrmann, et al.
European Journal of Pediatrics|November 1, 1985
A double-blind placebo controlled trial with oral ambroxol and N-acetylcysteine for mucolytic treatment in cystic fibrosisF Ratjen, R Wönne, H G Posselt, et al.
Gut|December 1, 1978
Gamma heavy chain disease simulating alpha chain diseaseS W Bender, F Danon, J L Preud'homme, et al.
European Journal of Pediatrics|October 1, 1994
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorderA C Sewell, S W Bender, S Wirth, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1983
Early diagnosis of intestinal non-Hodgkin lymphoma by endoscopyJ Hintze, H G Posselt, A Walther, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 1, 1984
Biochemical quantification of crypt hyperplastic villous atrophy by aldolase activity assayS W Bender, H G Posselt, M Stäps, et al.
European Journal of Pediatrics|April 3, 1979
Evaluation of long term tobramycin therapy in patients with cystic fibrosis and advanced pulmonary diseaseU Paporisz, H G Posselt, R Wönne, et al.
Padiatrie Und Padologie|January 1, 1987
Increased concentrations of HbAlab in hereditary fructose intolerance and galactosemiaH Böhles, J Schädle, W Endres, et al.
Pageof 6