Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W Marques

Showing results (11-20 of 45) with videos related to

Pageof 5
Sort By:
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 23, 2003
Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplicationW Marques, M G Sweeney, N W Wood
Acta Neurologica Scandinavica|August 3, 2004
Dejerine-Sottas' neuropathy caused by the missense mutation PMP22 Ser72LeuW Marques, J M Pina Neto, A A Barreira
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: various factors of relevance for diagnosis]W Marques Júnior, A A Barreira, R F Herrera
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: profile of patients without established etiological diagnosis]W Marques Júnior, R F Herrera, A A Barreira
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 6, 2000
Limitations on the clinical utility of the ulnar dorsal cutaneous sensory nerve action potentialA L Dutra de Oliveira, A A Barreira, W Marques
Physical Review Letters|July 22, 2015
Rayleigh-Brillouin Scattering in Binary-Gas MixturesZ Gu, W Ubachs, W Marques, et al.
Epilepsia|February 10, 1999
Male monozygotic twins discordant for periventricular nodular heterotopia and epilepsyS M Sisodiya, W Marques, A Everitt, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Muscle hemangiomatosis presenting as a severe feature in a patient with the pten mutation: expanding the phenotype of vascular malformations in bannayan-riley-ruvalcaba syndromeY Soysal, T Acun, Cm Lourenço, et al.
Muscle & Nerve|March 1, 1994
Postsurgical idiopathic brachial neuritisR I Malamut, W Marques, J D England, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: syndromic, topographic, and etiological diagnoses]W Marques Júnior, R F Herrera, E S Trade, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 23, 2003
Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplicationW Marques, M G Sweeney, N W Wood
Acta Neurologica Scandinavica|August 3, 2004
Dejerine-Sottas' neuropathy caused by the missense mutation PMP22 Ser72LeuW Marques, J M Pina Neto, A A Barreira
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: various factors of relevance for diagnosis]W Marques Júnior, A A Barreira, R F Herrera
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: profile of patients without established etiological diagnosis]W Marques Júnior, R F Herrera, A A Barreira
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 6, 2000
Limitations on the clinical utility of the ulnar dorsal cutaneous sensory nerve action potentialA L Dutra de Oliveira, A A Barreira, W Marques
Physical Review Letters|July 22, 2015
Rayleigh-Brillouin Scattering in Binary-Gas MixturesZ Gu, W Ubachs, W Marques, et al.
Epilepsia|February 10, 1999
Male monozygotic twins discordant for periventricular nodular heterotopia and epilepsyS M Sisodiya, W Marques, A Everitt, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Muscle hemangiomatosis presenting as a severe feature in a patient with the pten mutation: expanding the phenotype of vascular malformations in bannayan-riley-ruvalcaba syndromeY Soysal, T Acun, Cm Lourenço, et al.
Muscle & Nerve|March 1, 1994
Postsurgical idiopathic brachial neuritisR I Malamut, W Marques, J D England, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1992
[Diagnosis of peripheral neuropathies: syndromic, topographic, and etiological diagnoses]W Marques Júnior, R F Herrera, E S Trade, et al.
Pageof 5