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V Vedanarayanan

Showing results (21-30 of 29) with videos related to

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Muscle & Nerve|October 15, 1998
Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathyV V Vedanarayanan, S Smith, S H Subramony, et al.
Molecular Genetics and Metabolism|November 16, 2001
Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissuesF Tsien, B Sun, N E Hopkins, et al.
Journal of Neurosurgery|December 1, 1996
Expanding cyst of the septum pellucidum. Case reportJ A Lancon, D E Haines, F A Raila, et al.
Neurology|July 1, 1997
Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial diseaseR Fadic, J A Russell, V V Vedanarayanan, et al.
Neurology|February 28, 2002
Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotypeP C Scacheri, E M Gillanders, S H Subramony, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|September 8, 2012
Gastric dysmotility and low serum vitamin D levels in patients with gastroparesisA Kedar, Y Nikitina, O R Henry, et al.
Neurogastroenterology and Motility|December 6, 2017
Intravenous immunoglobulin in drug and device refractory patients with the symptoms of gastroparesis-an open-label studyM Ashat, A Lewis, H Liaquat, et al.
Neurology|December 13, 2000
A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathyP C Scacheri, E P Hoffman, J D Fratkin, et al.
Annals of Neurology|June 29, 2005
CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophyDiana M Escolar, Gunnar Buyse, Erik Henricson, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Muscle & Nerve|October 15, 1998
Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathyV V Vedanarayanan, S Smith, S H Subramony, et al.
Molecular Genetics and Metabolism|November 16, 2001
Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissuesF Tsien, B Sun, N E Hopkins, et al.
Journal of Neurosurgery|December 1, 1996
Expanding cyst of the septum pellucidum. Case reportJ A Lancon, D E Haines, F A Raila, et al.
Neurology|July 1, 1997
Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial diseaseR Fadic, J A Russell, V V Vedanarayanan, et al.
Neurology|February 28, 2002
Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotypeP C Scacheri, E M Gillanders, S H Subramony, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|September 8, 2012
Gastric dysmotility and low serum vitamin D levels in patients with gastroparesisA Kedar, Y Nikitina, O R Henry, et al.
Neurogastroenterology and Motility|December 6, 2017
Intravenous immunoglobulin in drug and device refractory patients with the symptoms of gastroparesis-an open-label studyM Ashat, A Lewis, H Liaquat, et al.
Neurology|December 13, 2000
A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathyP C Scacheri, E P Hoffman, J D Fratkin, et al.
Annals of Neurology|June 29, 2005
CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophyDiana M Escolar, Gunnar Buyse, Erik Henricson, et al.
Pageof 3