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B Wirth

Showing results (61-70 of 119) with videos related to

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Neuropediatrics|February 1, 1996
Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findingsS Rudnik-Schöneborn, R Forkert, E Hahnen, et al.
The American Journal of Physiology|April 13, 1999
Interactions between gastric volume and duodenal nutrients in the control of liquid gastric emptyingT H Moran, J B Wirth, G J Schwartz, et al.
International Journal of Sports Medicine|May 8, 2012
Whole body vibration added to endurance training in obese women - a pilot studyB Wilms, J Frick, B Ernst, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2000
Htra2-beta 1 stimulates an exonic splicing enhancer and can restore full-length SMN expression to survival motor neuron 2 (SMN2)Y Hofmann, C L Lorson, S Stamm, et al.
Journal of Back and Musculoskeletal Rehabilitation|March 23, 2016
Respiratory muscle endurance training reduces chronic neck pain: A pilot studyB Wirth, T Duarte Ferreira, M Mittelholzer, et al.
The Journal of Urology|January 1, 1996
Primary squamous cell carcinoma of the ureter and squamous adenocarcinoma of the renal pelvis: 2 case reportsI Papadopoulos, B Wirth, K Weichert-Jacobsen, et al.
Human Mutation|December 8, 2004
Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophyY Sun, M Grimmler, V Schwarzer, et al.
Diabetes Care|January 1, 1993
Prevalence and risk factors for diabetes and diabetes-related amputations in American Indians in southern ArizonaR B Wirth, A A Marfin, D W Grau, et al.
Journal of Medical Genetics|April 1, 1997
Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseasesS Spranger, S Rudnik-Schöneborn, M Spranger, et al.
Human Molecular Genetics|May 1, 1997
Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA)E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Pageof 12

Showing results (61-70 of 119) with videos related to

Sort By:
Pageof 12
Neuropediatrics|February 1, 1996
Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findingsS Rudnik-Schöneborn, R Forkert, E Hahnen, et al.
The American Journal of Physiology|April 13, 1999
Interactions between gastric volume and duodenal nutrients in the control of liquid gastric emptyingT H Moran, J B Wirth, G J Schwartz, et al.
International Journal of Sports Medicine|May 8, 2012
Whole body vibration added to endurance training in obese women - a pilot studyB Wilms, J Frick, B Ernst, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2000
Htra2-beta 1 stimulates an exonic splicing enhancer and can restore full-length SMN expression to survival motor neuron 2 (SMN2)Y Hofmann, C L Lorson, S Stamm, et al.
Journal of Back and Musculoskeletal Rehabilitation|March 23, 2016
Respiratory muscle endurance training reduces chronic neck pain: A pilot studyB Wirth, T Duarte Ferreira, M Mittelholzer, et al.
The Journal of Urology|January 1, 1996
Primary squamous cell carcinoma of the ureter and squamous adenocarcinoma of the renal pelvis: 2 case reportsI Papadopoulos, B Wirth, K Weichert-Jacobsen, et al.
Human Mutation|December 8, 2004
Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophyY Sun, M Grimmler, V Schwarzer, et al.
Diabetes Care|January 1, 1993
Prevalence and risk factors for diabetes and diabetes-related amputations in American Indians in southern ArizonaR B Wirth, A A Marfin, D W Grau, et al.
Journal of Medical Genetics|April 1, 1997
Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseasesS Spranger, S Rudnik-Schöneborn, M Spranger, et al.
Human Molecular Genetics|May 1, 1997
Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA)E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Pageof 12