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M M Reilly

Showing results (21-30 of 61) with videos related to

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Brain : a Journal of Neurology|May 4, 2001
Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelinH Houlden, R H King, N W Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Treatment of chronic inflammatory demyelinating polyradiculoneuropathy with methotrexateD Fialho, Y-C Chan, D C Allen, et al.
Neurology|October 4, 2008
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2H Houlden, M Laura, F Wavrant-De Vrièze, et al.
Neurology|September 25, 1998
Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathyV Planté-Bordeneuve, T Lalu, M Misrahi, et al.
Clinical Genetics|July 7, 2012
Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patientsG Koutsis, A Pandraud, G Karadima, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2005
Syncope associated with pain as the presenting feature of neck malignancy: failure of cardiac pacemaker to prevent attacks in two casesP F Worth, J C Stevens, F Lasri, et al.
Neurology|September 27, 2006
CSF neurofilament levels: a potential prognostic marker in Guillain-Barré syndromeA Petzold, N Hinds, N M F Murray, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2002
Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA?P Garrard, J Blake, V Stinton, et al.
NMR in Biomedicine|July 29, 2011
Correcting radiofrequency inhomogeneity effects in skeletal muscle magnetisation transfer mapsC D J Sinclair, J M Morrow, M G Hanna, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 20, 2002
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseM-J Lee, I Nelson, H Houlden, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Brain : a Journal of Neurology|May 4, 2001
Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelinH Houlden, R H King, N W Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Treatment of chronic inflammatory demyelinating polyradiculoneuropathy with methotrexateD Fialho, Y-C Chan, D C Allen, et al.
Neurology|October 4, 2008
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2H Houlden, M Laura, F Wavrant-De Vrièze, et al.
Neurology|September 25, 1998
Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathyV Planté-Bordeneuve, T Lalu, M Misrahi, et al.
Clinical Genetics|July 7, 2012
Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot-Marie-Tooth type 1 patientsG Koutsis, A Pandraud, G Karadima, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2005
Syncope associated with pain as the presenting feature of neck malignancy: failure of cardiac pacemaker to prevent attacks in two casesP F Worth, J C Stevens, F Lasri, et al.
Neurology|September 27, 2006
CSF neurofilament levels: a potential prognostic marker in Guillain-Barré syndromeA Petzold, N Hinds, N M F Murray, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2002
Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA?P Garrard, J Blake, V Stinton, et al.
NMR in Biomedicine|July 29, 2011
Correcting radiofrequency inhomogeneity effects in skeletal muscle magnetisation transfer mapsC D J Sinclair, J M Morrow, M G Hanna, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 20, 2002
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseM-J Lee, I Nelson, H Houlden, et al.
Pageof 7