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P. Evrard

Université catholique de Louvain

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Featured researches published by P. Evrard.

Archive | 1972

An Unusual Case of GM2-Gangliosidosis with Deficiency of Hexosaminidase A and B

F. Van Hoof; P. Evrard; Hg. Hers

In this report, we briefly describe a patient with GM2-gangliosidosis having a deficiency in both isoenzymes of N-acetyl-β-hexosaminidase and displaying several clinical, ultrastructural and enzymatic particularities.

Prenatal Diagnosis | 1988

Prenatal diagnosis of Hunter syndrome using fetal plasma.

W. Lissens; M. Van Lierde; J. Decaluwe; W. Foulon; P. Evrard; F. Van Hoof; M. Freund; I. Liebaers

Neuroscience Research Supplements | 1987

Fascicular organization of the radial glial fibers in developing murine neocortex: An immunohistochemical study combined with 3H thymidine autoradiography

J.-F. Gadisseux; P. Evrard; Jean-Paul Misson; Verne S. Caviness

Acta paediatrica Belgica | 1990

Histogenèse du cortex cérébral et migration neuronale

Jean-Paul Misson; Takao Takahashi; C. Austin; Jean-François Gadisseux; P. Evrard; Verne S. Caviness

La vida humana, origen y desarrollo: reflexiones bioéticas de científicos y moralistas, 1989, ISBN 84-85281-86-1, págs. 127-152 | 1989

Las malformaciones del sistema nervioso central

P. Evrard; Jean François Gadisseux; Gilles Lyon

Neuroscience | 1988

Identification of radial glial growth cones

Jean-Paul Misson; P. Evrard; J.-F. Gadisseux; Verne S. Caviness

Neuroscience | 1988

Glial organization in the developing reeler neocortex

J.-F. Gadisseux; P. Evrard; Jean-Paul Misson; Verne S. Caviness

Journal de génétique humaine | 1988

Syndrome de Hunter: premier diagnostic prénatal sur sang foetal

M. Freund; S. Gosseye; M. Van Lierde; W. Lissens; J. Decaluwe; W. Foulon; P. Evrard; F. Van Hoof; I. Liebaers; P. De St-Georges; H. Kadhim; R De Meyer

American Journal of Pathology | 1986

Multiple peroxysomal deficiency syndromes: a comparative and multidisciplinary study in Zellweger and Neonatal Adrenoleukodystrophy patients

Joseph Vamecq; Jp. Draye; François Van Hoof; Jean-Paul Misson; P. Evrard; G. Verellen; J. Van Eldere; H. Eyssen; R. B. H. Schutgens; R. J. A. Wanders; Frank Roels; S. L. Gloldfischer

Archive | 1985

Maladie de Zellweger et adrenoleukodystrophie néonatale: une même maladie ou deux affections distinctes?

Jean-Paul Misson; P. Evrard; G. Verellen; D. Claus; J.-M. Guerit; J. Van Eldere; H. Eyssen; R. B. H. Schutgens; F. Van Hoof; J. Vamecq

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Jean-Paul Misson

University of Liège

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F. Van Hoof

Catholic University of Leuven

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Verne S. Caviness

Harvard University

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H. Eyssen

Katholieke Universiteit Leuven

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J. Van Eldere

Katholieke Universiteit Leuven

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R. B. H. Schutgens

University of Amsterdam

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M. Freund

Université catholique de Louvain

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M. Van Lierde

Université catholique de Louvain

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Frank Roels

Ghent University

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François Van Hoof

Université catholique de Louvain

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