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1
Cysticercosis official report to main theme tropical neurology
Cysticercosis official report to main theme tropical neurology
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Cysticercosis official report to main theme tropical neurology

A Spina Franca World Congress of Neurology (14. 1989 New Delhi)

v.37, n.supl., p.120, 1989 Neurology India

1989

Localização: FM - Fac. Medicina    (BCSEP 1989 132 )(Acessar)

2
Self-Organizing Maps as a Complementary and Non-Invasive Technique for the Analysis of Brain Tumors
Self-Organizing Maps as a Complementary and Non-Invasive Technique for the Analysis of Brain Tumors
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Self-Organizing Maps as a Complementary and Non-Invasive Technique for the Analysis of Brain Tumors

Paulo Afonso Mei Cleyton de Carvalho Carneiro 1980-; Stephen James Fraser; Li Li Min; Fabiano Reis; Annual Meeting of the American Academy of Neurology (65. 2013 San Diego)

Wolters Kluwer Health Neurology v. 80 n. 7 Supplement

San Diego American Academy of Neurology 2013

Item não circula. Consulte sua biblioteca.(Acessar)

3
NEUROCAD a neurology computer-aided toolkit
NEUROCAD a neurology computer-aided toolkit
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

NEUROCAD a neurology computer-aided toolkit

L. F. Oliveira L Cavalcanti; M. C Oliveira; G. F Caetano; Paulo Mazzoncini de Azevedo-Marques; International Congress on Computer Assisted Radiology and Surgery (16. 2002 Paris)

Proceedings Paris : Springer, 2002

Paris Springer 2002

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1263946 ) e outros locais(Acessar)

4
A descriptive study of a Brazilian population with early onset chronic peripheral polyneuropathy
A descriptive study of a Brazilian population with early onset chronic peripheral polyneuropathy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A descriptive study of a Brazilian population with early onset chronic peripheral polyneuropathy

Wilson Marques Júnior Vinicius S Borghetti; Vanessa D Marques; Amilton Antunes Barreira; American Academy of Neurology Annual Meeting (59. 2007 Boston)

Neurology Minneapolis v. 68, suppl. 1, p. A68, 2007

Minneapolis 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (PCD 1611742 ) e outros locais(Acessar)

5
Familial neuromyelitis optica
Familial neuromyelitis optica
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Familial neuromyelitis optica

Marcelo Matiello Doralina G Brum; Amilton Antunes Barreira; Daniel Kingsbury; Brian Weinshenker; Annual Meeting of The American Academy of Neurology (60. 2008 Chicago)

Neurology Philadelphia v. 70, n. 11, suppl. 1, p. A266, res. P05.054, 2008

Philadelphia 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1669315 ) e outros locais(Acessar)

6
Nerve conduction studies in leprosy contactants
Nerve conduction studies in leprosy contactants
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Nerve conduction studies in leprosy contactants

Wilson Marques Júnior Vanessa Daccach Marques; Renata Bazan Furini; Norma Tiraboschi Foss; Annual Meeting of the American Academy of Neurology (61. 2009 Seattle)

Neurology Philadelphia v. 72, n. 11 suppl. 3, p. A219, res. P05.052, 2009

Philadelphia 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1775959 ) e outros locais(Acessar)

7
A de novo novel mutation in MFN2 associated with early onset, severe neuropathy and learning problems
A de novo novel mutation in MFN2 associated with early onset, severe neuropathy and learning problems
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A de novo novel mutation in MFN2 associated with early onset, severe neuropathy and learning problems

Wilson Marques Júnior Adriana Genari; Vinicius H. S Borghtti; Silmara P. G Lima; Antônio Carlos dos Santos; Amilton Antunes Barreira; Annual Meeting of The American Academy of Neurology (60. 2008 Chicago)

Neurology Philadelphia v. 70, n. 11, suppl. 1, p. A312, res. P06.053, 2008

Philadelphia 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1669348 ) e outros locais(Acessar)

8
Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy
Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Relevance of the A8344G and T8356C mtDNA mutation analyses in the approach of progressive myoclonic epilepsy

Antonio M. P Omuro Umbertina Conti Reed; Suely Kazue Nagahashi Marie; Mariz Vainzof; Mary S Carvalho; Monica Rusticci; Simone A Fernandes; American Academy of Neurology Annual Meeting (51. 1999 Canada)

Neurology Canada v. 52, n. 06, supl. 06, p. A51, res. P04.047, 1999

Canada 1999

Localização: FM - Fac. Medicina    (BCSEP 246 1999 ) e outros locais(Acessar)

9
Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy
Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Screening for mutation in the "alfa" 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in patients with malignant-hyperthemia and central core myopathy

Mariz Vainzof Monica S Rusticci; Suely Kazue Nagahashi Marie; Mayana Zatz; Ana Maria Crous Tsanaclis; Helga Cristina Almeida da Silva; American Academy of Neurology Annual Meeting (51. 1999 Canada)

Neurology Canada v. 52, n. 06, supl. 06, p. A331, res. P04.038, 1999

Canada 1999

Localização: FM - Fac. Medicina    (BCSEP 246 1999 ) e outros locais(Acessar)

10
A mild and unusual CMT compound phenotype due to the presence of two mutations in pmP22 gene 17p duplication and Ser72Leuc
A mild and unusual CMT compound phenotype due to the presence of two mutations in pmP22 gene 17p duplication and Ser72Leuc
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A mild and unusual CMT compound phenotype due to the presence of two mutations in pmP22 gene 17p duplication and Ser72Leuc

Wilson Marques Júnior Silmara S. P. G Lima; Vinicius H. S Borghtti; Keity C Bueno; Amilton Antunes Barreira; Annual Meeting of The American Academy of Neurology (60. 2008 Chicago)

Neurology Philadelphia v. 70, n. 11, suppl. 1, p. A313, res. P06.058, 2008

Philadelphia 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1669388 ) e outros locais(Acessar)

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Deste Autor:

  1. Teixeira, M
  2. World Congress of Neurology
  3. Nitrini, R
  4. Reed, U
  5. Barreira, A

Neste Assunto:

  1. Neurologia
  2. Fisiologia
  3. Epilepsia
  4. Acidente Vascular Cerebral
  5. Anatomia

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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