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1
Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I
Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I
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Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I

K. C. Bueno S. P Gouvêa; C. M Lourenço; Wilson Marques Júnior; Meeting of The Peripheral Nerve Society (2011 Potomac)

Journal of The Peripheral Nervous System Hoboken v. 16, suppl. 3, p. S14-S15, 2011

Hoboken 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2220858 Estantes Deslizantes ) e outros locais(Acessar)

2
Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS) Andermann syndrome
Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS) Andermann syndrome
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Increasing the differential diagnosis of the inherited demyelinating neuropathies with non-uniform nerve conduction(NCS) Andermann syndrome

Wilson Marques Júnior C. M Lourenço; V. D Marques; M. V Gonçalves; Cláudia Ferreira da Rosa Sobreira; Amilton Antunes Barreira; Meeting of The Peripheral Nerve Society (2009 Würzburg)

Journal of The Peripheral Nervous System Malden v. 14, suppl. 2, p. 97-98, 2009

Malden 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1772643 ) e outros locais(Acessar)

3
Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort
Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort
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Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort

A. M Rocha P. J Tomaselli; S. P Gouvea; F. B Figueiredo; C. M Lourenço; Wilson Marques Júnior; Meeting of Peripheral Nerve Society (2017 Barcelona)

Journal of the Peripheral Nervous System Hoboken v. 22, p. 367-368, 2017

Hoboken 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2921669 Estantes Deslizantes )(Acessar)

4
A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities
A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities
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A patient with ataxia with oculomotor apraxia type 1 and slow conduction velocities

P. J Tomaselli C. M Lourenço; V. P Cintra; Amilton Antunes Barreira; Wilson Marques Júnior; Meeting of Peripheral Nerve Society (2017 Barcelona)

Journal of the Peripheral Nervous System Hoboken v. 22, p. 397, 2017

Hoboken 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2921676 Estantes Deslizantes )(Acessar)

5
Identification of five novel mutations in brazilian families with X-linked CMT
Identification of five novel mutations in brazilian families with X-linked CMT
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Identification of five novel mutations in brazilian families with X-linked CMT

P. J Tomaselli S. P Gouvea; K. F. S Nyshyama; N Nicolau Junior; C. M Lourenço; Wilson Marques Júnior; Meeting of Peripheral Nerve Society (2017 Barcelona)

Journal of the Peripheral Nervous System Hoboken v. 22, p. 396, 2017

Hoboken 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2921670 Estantes Deslizantes )(Acessar)

6
Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction andermann syndrome
Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction andermann syndrome
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Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction andermann syndrome

Charles M. Lourenço Nicolas Dupré; Jean-Baptiste Rivière; Guy A Rouleau; Vanessa D Marques; Adriana B Genari; Antônio Carlos dos Santos; Amilton Antunes Barreira; Wilson Marques Júnior

Journal of the Peripheral Nervous System Hoboken v. 17, n. 1, p. 123-127, 2012

Hoboken 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2399588 Estantes Deslizantes )(Acessar)

7
Does pregnancy change the natural history of CMT1A neuropathy?
Does pregnancy change the natural history of CMT1A neuropathy?
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Does pregnancy change the natural history of CMT1A neuropathy?

R. de Cassia Carvalho J. S Algemiro; V. D Marques; P. J Tomaselli; P. T Onofre; C. M Lourenço; Wilson Marques Júnior; Meeting of the Peripheral Nerve Society (2013 Saint-Malo)

Journal of the Peripheral Nervous System Hoboken v. 18, suppl., p. S29-S30, 2013

Hoboken 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2438731 Estantes Deslizantes )(Acessar)

8
GDPA1 mutations in brazilian patients with CMT2, CMT2-AR and CMT4
GDPA1 mutations in brazilian patients with CMT2, CMT2-AR and CMT4
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GDPA1 mutations in brazilian patients with CMT2, CMT2-AR and CMT4

F. Barbosa Figueiredo Wilson Araújo da Silva Júnior; C. M Lourenço; S. P Gouvêa; Wilson Marques Júnior; International Charcot-Marie-Tooth and Related Neuropathy Consortium (CMTR) Meeting (6. 2016 Hoboken)

Journal of the Peripheral Nervous System Hoboken v. 21, n. 3, p. 238, 2016

Hoboken 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2855659 Estantes Deslizantes )(Acessar)

9
High glucose level as a modifier factor in CMT1A patients
High glucose level as a modifier factor in CMT1A patients
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High glucose level as a modifier factor in CMT1A patients

Juliana B. Secchin Rita C. C Leal; Charles M Lourenço; Vanessa Daccach Marques; Patricia T. L Nogueira; Andre C. J Santos; Pedro J Tomaselli; Wilson Marques Júnior

Journal of the Peripheral Nervous System Hoboken v. 25, n. 2, p. 132-137, 2020

Hoboken 2020

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3134568 Acervo Digital )(Acessar)

10
High glucose level as a modifier factor in CMT1A patients
High glucose level as a modifier factor in CMT1A patients
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Artigo 		Adicionar ao Meu Espaço

High glucose level as a modifier factor in CMT1A patients

Secchin, Juliana B. ; Leal, Rita C. C. ; Lourenço, Charles M. ; Marques, V. D. ; Nogueira, Patricia T. L. ; Santos, Andre C. J. ; Tomaselli, Pedro J. ; Marques, Wilson

Journal of the peripheral nervous system, 2020-06, Vol.25 (2), p.132-137 [Periódico revisado por pares]

Malden, USA: Wiley Periodicals, Inc

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