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D Hilton-Jones

Showing results (51-60 of 58) with videos related to

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European Journal of Neurology|July 13, 2006
Guidelines for the treatment of autoimmune neuromuscular transmission disordersG O Skeie, S Apostolski, A Evoli, et al.
Neuromuscular Disorders : NMD|May 1, 1995
Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Neuropediatrics|August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxityE Mercuri, A Lampe, V Straub, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UKS Figueroa-Bonaparte, J Hudson, R Barresi, et al.
Neurology|May 4, 2012
Myasthenia gravis and neuromyelitis optica spectrum disorder: a multicenter study of 16 patientsM I Leite, E Coutinho, M Lana-Peixoto, et al.
Neurology|October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variationN P Davies, P Imbrici, D Fialho, et al.
Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
European Journal of Neurology|July 13, 2006
Guidelines for the treatment of autoimmune neuromuscular transmission disordersG O Skeie, S Apostolski, A Evoli, et al.
Neuromuscular Disorders : NMD|May 1, 1995
Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.
European Journal of Neurology|May 1, 2013
EFNS review on the role of muscle biopsy in the investigation of myalgiaT Kyriakides, C Angelini, J Schaefer, et al.
Neuropediatrics|August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxityE Mercuri, A Lampe, V Straub, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UKS Figueroa-Bonaparte, J Hudson, R Barresi, et al.
Neurology|May 4, 2012
Myasthenia gravis and neuromyelitis optica spectrum disorder: a multicenter study of 16 patientsM I Leite, E Coutinho, M Lana-Peixoto, et al.
Neurology|October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variationN P Davies, P Imbrici, D Fialho, et al.
Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.
Pageof 6