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Hammans

Showing results (41-50 of 87) with videos related to

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Muscle & Nerve|February 26, 2004
MNGIE neuropathy: five cases mimicking chronic inflammatory demyelinating polyneuropathyRichard S Bedlack, Tuan Vu, Simon Hammans, et al.
Neuromuscular Disorders : NMD|June 29, 2010
Calpainopathy presenting as foot drop in a 41 year oldG Burke, C Hillier, J Cole, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2010
Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophySacha Ferdinandusse, Simon Barker, Katherine Lachlan, et al.
Neuromuscular Disorders : NMD|February 6, 2021
Desminopathy presenting as late onset bilateral facial weakness, with diagnosis supported by lower limb MRILiam S Carroll, Mark Walker, David Allen, et al.
Human Mutation|May 20, 2003
A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneityP Jagiello, C Hammans, S Wieczorek, et al.
Fetal Diagnosis and Therapy|May 1, 1997
On the complication risk of early amniocentesis versus standard amniocentesisB Eiben, W Hammans, S Hansen, et al.
Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.
Journal of Surgical Case Reports|July 27, 2018
Small bowel obstruction SBO after TAPP repair caused by a self-anchoring barbed suture device for peritoneal closure: case reportEugenio M Tagliaferri, Sheng L Wong Tavara, Jacky L Abad de Jesus, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.
Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.
Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:
Pageof 9
Muscle & Nerve|February 26, 2004
MNGIE neuropathy: five cases mimicking chronic inflammatory demyelinating polyneuropathyRichard S Bedlack, Tuan Vu, Simon Hammans, et al.
Neuromuscular Disorders : NMD|June 29, 2010
Calpainopathy presenting as foot drop in a 41 year oldG Burke, C Hillier, J Cole, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2010
Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophySacha Ferdinandusse, Simon Barker, Katherine Lachlan, et al.
Neuromuscular Disorders : NMD|February 6, 2021
Desminopathy presenting as late onset bilateral facial weakness, with diagnosis supported by lower limb MRILiam S Carroll, Mark Walker, David Allen, et al.
Human Mutation|May 20, 2003
A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneityP Jagiello, C Hammans, S Wieczorek, et al.
Fetal Diagnosis and Therapy|May 1, 1997
On the complication risk of early amniocentesis versus standard amniocentesisB Eiben, W Hammans, S Hansen, et al.
Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.
Journal of Surgical Case Reports|July 27, 2018
Small bowel obstruction SBO after TAPP repair caused by a self-anchoring barbed suture device for peritoneal closure: case reportEugenio M Tagliaferri, Sheng L Wong Tavara, Jacky L Abad de Jesus, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.
Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.
Pageof 9