Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology-Reference-Cited by-同舟云学术

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Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology

Published:2005-02-16 Issue:4 Volume:109 Page:433-442
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Aronica E.,van Kempen A. A. M. W.,van der Heide M.,Poll-The B. T.,van Slooten H. J.,Troost D.,Rozemuller-Kwakkel J. M.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-004-0975-3.pdf

Reference51 articles.

1. Antoun H, Villeneuve N, Gelot A, Panisset S, Adamsbaum C (1999) Cerebellar atrophy: an important feature of carbohydrate deficient glycoprotein syndrome type 1. Pediatr Radiol 29:194–198

2. Aronica E, Leenstra S, Jansen GH, Veelen CW van, Yankaya B, Troost D (2001) Expression of brain-derived neurotrophic factor and tyrosine kinase B receptor proteins in glioneuronal tumors from patients with intractable epilepsy: colocalization with N-methyl-d-aspartic acid receptor. Acta Neuropathol 101:383–392

3. Aronica E, Gorter JA, Jansen GH, Veelen CW van, Rijen PC van, Ramkema M, Troost D (2003) Expression and cell distribution of group I and group II metabotropic glutamate receptor subtypes in taylor-type focal cortical dysplasia. Epilepsia 44:785–795

4. Barth PG (1993) Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset. Brain Dev 15:411–422

5. Barth PG, Wanders RJ, Ruitenbeek W, Roe C, Scholte HR, Harten H van der, Moorsel J van, Duran M, Dingemans KP (1998) Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families. Neuromuscul Disord 8:296–304

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