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B Wirth

Showing results (51-60 of 119) with videos related to

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European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophyC L Lorson, E Hahnen, E J Androphy, et al.
The Journal of Urology|February 1, 1997
Panurothelial condyloma acuminatum with development of squamous cell carcinoma of the bladder and renal pelvisT Brüske, T Loch, O Thiemann, et al.
Prenatal Diagnosis|May 1, 1995
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 casesB Wirth, S Rudnik-Schöneborn, E Hahnen, et al.
Ground Water|December 8, 2018
Exploring Geological and Topographical Controls on Low Flows with Hydrogeological ModelsClaire Carlier, Stefanie B Wirth, Fabien Cochand, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degenerationS Rudnik-Schöneborn, B Wirth, D Röhrig, et al.
Manual Therapy|May 20, 2014
Respiratory dysfunction in patients with chronic neck pain - influence of thoracic spine and chest mobilityB Wirth, M Amstalden, M Perk, et al.
American Journal of Medical Genetics|May 15, 1994
Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implicationsS Rudnik-Schöneborn, D Röhrig, G Morgan, et al.
American Journal of Human Genetics|November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the diseaseE Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 11, 2011
Is a positive clinical outcome after exercise therapy for chronic non-specific low back pain contingent upon a corresponding improvement in the targeted aspect(s) of performance? A systematic reviewF Steiger, B Wirth, E D de Bruin, et al.
Pageof 12

Showing results (51-60 of 119) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophyC L Lorson, E Hahnen, E J Androphy, et al.
The Journal of Urology|February 1, 1997
Panurothelial condyloma acuminatum with development of squamous cell carcinoma of the bladder and renal pelvisT Brüske, T Loch, O Thiemann, et al.
Prenatal Diagnosis|May 1, 1995
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 casesB Wirth, S Rudnik-Schöneborn, E Hahnen, et al.
Ground Water|December 8, 2018
Exploring Geological and Topographical Controls on Low Flows with Hydrogeological ModelsClaire Carlier, Stefanie B Wirth, Fabien Cochand, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degenerationS Rudnik-Schöneborn, B Wirth, D Röhrig, et al.
Manual Therapy|May 20, 2014
Respiratory dysfunction in patients with chronic neck pain - influence of thoracic spine and chest mobilityB Wirth, M Amstalden, M Perk, et al.
American Journal of Medical Genetics|May 15, 1994
Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implicationsS Rudnik-Schöneborn, D Röhrig, G Morgan, et al.
American Journal of Human Genetics|November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the diseaseE Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 11, 2011
Is a positive clinical outcome after exercise therapy for chronic non-specific low back pain contingent upon a corresponding improvement in the targeted aspect(s) of performance? A systematic reviewF Steiger, B Wirth, E D de Bruin, et al.
Pageof 12