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Surgical Neurology
|
June 29, 2007
Dorsal root ganglionectomy for the diagnosis of sensory neuropathies. Surgical technique and results
Benedicto Oscar Colli, Carlos Gilberto Carlotti, João Alberto Assirati, et al.
Neurogenetics
|
August 26, 2009
Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes
Silmara P Gouvea, Vinícius H S Borghetti, Keity C Bueno, et al.
Revista Latino-Americana De Enfermagem
|
January 18, 2012
Cultural adaptation and validation of the Neuropathy - and Foot Ulcer - Specific Quality of Life instrument (NeuroQol) for Brazilian Portuguese - Phase 1
Antonia Tayana da Franca Xavier, Milton Cesar Foss, Wilson Marques Junior, et al.
Journal of Neurology
|
June 19, 2009
Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington's disease
Guilherme Riccioppo Rodrigues, Carolina Pinto Souza, Roberto Satler Cetlin, et al.
Journal of Neurology
|
March 15, 2005
17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population
Wilson Marques, Marcos R Freitas, Osvaldo J M Nascimento, et al.
Arquivos De Neuro-Psiquiatria
|
December 23, 2008
Swallowing dysfunction in hereditary neuropathy with liability to pressure palsies
Paulo J Lorenzoni, Rosana H Scola, Juliana Cardoso, et al.
Cerebellum (London, England)
|
June 28, 2019
Frequency and Genetic Profile of Compound Heterozygous Friedreich's Ataxia Patients-the Brazilian Experience
Thiago Mazzo Peluzzo, Luciana Cardoso Bonadia, Amanda Donatti, et al.
Memorias Do Instituto Oswaldo Cruz
|
September 7, 2011
Early detection of leprosy by examination of household contacts, determination of serum anti-PGL-1 antibodies and consanguinity
Renata Bazan-Furini, Ana Carolina F Motta, João Carlos L Simão, et al.
Arquivos De Neuro-Psiquiatria
|
July 15, 2011
Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype
Guilherme Riccioppo Rodrigues, Ruth H Walker, Benedikt Bader, et al.
Journal of the Peripheral Nervous System : JPNS
|
May 24, 2019
New novel mutations in Brazilian families with X-linked Charcot-Marie-Tooth disease
Silmara P Gouvea, Pedro J Tomaselli, Luiza S Barretto, et al.
Page
of 20
Search research articles
Search
Showing results (71-80 of 197) with videos related to
Sort By:
Page
of 20
Surgical Neurology
|
June 29, 2007
Dorsal root ganglionectomy for the diagnosis of sensory neuropathies. Surgical technique and results
Benedicto Oscar Colli, Carlos Gilberto Carlotti, João Alberto Assirati, et al.
Neurogenetics
|
August 26, 2009
Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes
Silmara P Gouvea, Vinícius H S Borghetti, Keity C Bueno, et al.
Revista Latino-Americana De Enfermagem
|
January 18, 2012
Cultural adaptation and validation of the Neuropathy - and Foot Ulcer - Specific Quality of Life instrument (NeuroQol) for Brazilian Portuguese - Phase 1
Antonia Tayana da Franca Xavier, Milton Cesar Foss, Wilson Marques Junior, et al.
Journal of Neurology
|
June 19, 2009
Use of the frontal assessment battery in evaluating executive dysfunction in patients with Huntington's disease
Guilherme Riccioppo Rodrigues, Carolina Pinto Souza, Roberto Satler Cetlin, et al.
Journal of Neurology
|
March 15, 2005
17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population
Wilson Marques, Marcos R Freitas, Osvaldo J M Nascimento, et al.
Arquivos De Neuro-Psiquiatria
|
December 23, 2008
Swallowing dysfunction in hereditary neuropathy with liability to pressure palsies
Paulo J Lorenzoni, Rosana H Scola, Juliana Cardoso, et al.
Cerebellum (London, England)
|
June 28, 2019
Frequency and Genetic Profile of Compound Heterozygous Friedreich's Ataxia Patients-the Brazilian Experience
Thiago Mazzo Peluzzo, Luciana Cardoso Bonadia, Amanda Donatti, et al.
Memorias Do Instituto Oswaldo Cruz
|
September 7, 2011
Early detection of leprosy by examination of household contacts, determination of serum anti-PGL-1 antibodies and consanguinity
Renata Bazan-Furini, Ana Carolina F Motta, João Carlos L Simão, et al.
Arquivos De Neuro-Psiquiatria
|
July 15, 2011
Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype
Guilherme Riccioppo Rodrigues, Ruth H Walker, Benedikt Bader, et al.
Journal of the Peripheral Nervous System : JPNS
|
May 24, 2019
New novel mutations in Brazilian families with X-linked Charcot-Marie-Tooth disease
Silmara P Gouvea, Pedro J Tomaselli, Luiza S Barretto, et al.
Page
of 20