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1
Childhood degos disease with prominent neurological symptoms report of a clinicopathological case
Childhood degos disease with prominent neurological symptoms report of a clinicopathological case
Material Type:
Artigo 		Adicionar ao Meu Espaço

Childhood degos disease with prominent neurological symptoms report of a clinicopathological case

Sérgio Rosemberg M B S Lopes; Mírian Nacagami Sotto; M S Graudenz

v.3 , p.42-6, jan. 1988 Journal of Child Neurology

1988

Localização: FM - Fac. Medicina    (BCSEP 1988 020 )(Acessar)

2
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system report of five atypical cases
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system report of five atypical cases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system report of five atypical cases

Umbertina Conti Reed Suely Kazue Nagahashi Marie; Mariz Vainzof; L. F Gobbo; J. E. P Gurgel; M. S Carvalho; M. B. D Resende; A. A Espindola; Mayana Zatz; Aron Judka Diament

Journal of Child Neurology v. 15, n. 3, p. 172-8, 2000

2000

Localização: FM - Fac. Medicina    (BCSEP 2000 315 )(Acessar)

3
Rasmussen encephalitis associated with segmental vitiligo of the scalp clinicopathologic report
Rasmussen encephalitis associated with segmental vitiligo of the scalp clinicopathologic report
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Rasmussen encephalitis associated with segmental vitiligo of the scalp clinicopathologic report

Elza Márcia T. Yacubian Sérgio Rosemberg; Theodomiro L Garrido Neto; Suely Kazue Nagahashi Marie; Rosa M. F Valério; Carmen Lisa Jorge

Journal of Child Neurology v. 16, n. 05, p. 374-377, May, 2001

Hamilton 2001

Localização: FM - Fac. Medicina    (BCSEP 2001 262 )(Acessar)

4
Calpainopathy focus on a pediatric population
Calpainopathy focus on a pediatric population
Material Type:
Artigo 		Adicionar ao Meu Espaço

Calpainopathy focus on a pediatric population

H. Kolski A. B Edmonton; J Vajsar; F de Paula; Mayana Zatz

Journal of Child Neurology v. 18, n. 3, p. 212, mar.2003

Hamilton 2003

Item não circula. Consulte sua biblioteca.(Acessar)

5
Rod distribution and muscle fiber type modification in the progression of nemaline myopathy
Rod distribution and muscle fiber type modification in the progression of nemaline myopathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Rod distribution and muscle fiber type modification in the progression of nemaline myopathy

J. Gurgel-Giannetti E Zanoteli; L. C Werneck; Umbertina Conti Reed; A. H Beggs; Suely Kazue Nagahashi Marie; M. A. T Fireman; A. S. B Oliveira; Mayana Zatz; Mariz Vainzof

Journal of Child Neurology v. 18, n. 3, p. 235-240, 2003

Saint Lois 2003

Localização: FM - Fac. Medicina    (BCSEP 2003 258 )(Acessar)

6
Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil
Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil

Roberto Rozenberg Fernando Kok; Maira Graeff Burin; M. C. Sá Miranda; C Vasques; A. M. M Henriques-Souza; R Gugliani; Mariz Vainzof; Lygia da Veiga Pereira

Journal of Child Neurology v. 21, n. 6, p. 540-544, 2006

Littleton 2006

Item não circula. Consulte sua biblioteca.(Acessar)

7
Consensus statement on standard of care for congenital myopathies
Consensus statement on standard of care for congenital myopathies
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Consensus statement on standard of care for congenital myopathies

Ching H Wang James J Dowling; Kathryn North; Mary K Schroth; Thomas Sejersen; Frederic Shapiro; Jonathan Bellini; Hali Weiss; Marc Guillet; Kimberly Amburgey; Susan Apkon; Enrico Bertini; Carsten Bonnemann; Nigel Clarke; Anne M Connolly; Brigitte Estournet-Mathiaud; Dominic Fitzgerald; Julaine M Florence; Richard Gee; Juliana Gurgel Giannetti; Allan M Glanzman; Brittany Hofmeister; Heinz Jungbluth; Anastassios C Koumbourlis; Nigel G Laing; Marion Main; Leslie A Morrison; Craig Munns; Kristy Rose; Pamela M Schuler; Caroline Sewry; Kari Storhaug; Mariz Vainzof; Nanci Yuan

Journal of Child Neurology Thousand Oaks, CA v. 37, n. 3, p. 363-382, 2012

Thousand Oaks, CA 2012

Item não circula. Consulte sua biblioteca.(Acessar)

8
Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population
Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population
Material Type:
Artigo 		Adicionar ao Meu Espaço

Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population

Edward Araujo Júnior Wellington de Paula Martins; Luciano Marcondes Machado Nardozza; Claudio Rodrigues Pires; Sebastião Marques Zanforlin Filho

Journal of Child Neurology Thousand Oaks v. 30, n. 2, p. 250-253, 2015

Thousand Oaks 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2716480 Estantes Deslizantes )(Acessar)

9
Calpainopathy focus on a pediatric population
Calpainopathy focus on a pediatric population
Material Type:
Artigo 		Adicionar ao Meu Espaço

Calpainopathy focus on a pediatric population

H. Kolski A. B Edmonton; J Vajsar; F de Paula; Mayana Zatz

Journal of Child Neurology v. 18, n. 3, p. 212, mar.2003

Hamilton 2003

Item não circula. Consulte sua biblioteca.(Acessar)

10
Childhood degos disease with prominent neurological symptoms report of a clinicopathological case
Childhood degos disease with prominent neurological symptoms report of a clinicopathological case
Material Type:
Artigo 		Adicionar ao Meu Espaço

Childhood degos disease with prominent neurological symptoms report of a clinicopathological case

Sérgio Rosemberg M B S Lopes; Mírian Nacagami Sotto; M S Graudenz

v.3 , p.42-6, jan. 1988 Journal of Child Neurology

1988

Localização: FM - Fac. Medicina    (BCSEP 1988 020 )(Acessar)

Resultados de 1 a 10 de 13  para Produção Intelectual da USP

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Deste Autor:

  1. Vainzof, M
  2. Marie, S
  3. Zatz, M
  4. Rosemberg, S
  5. Gurgel-Giannetti, J

Neste Assunto:

  1. Neurologia
  2. Mutação Genética
  3. Distrofia Muscular
  4. Doenças Metabólicas
  5. Sinais E Sintomas

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

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