(Q41934154)

14 October 2017

title

Pelizaeus-Merzbacher disease. The Löwenberg-Hill type (English)

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14 October 2017

G W Bruyn

1

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14 October 2017

H R Weenink

2

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14 October 2017

G T Bots

3

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14 October 2017

J L Teepen

4

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14 October 2017

W J van Wolferen

5

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14 October 2017

publication date

1 January 1985

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14 October 2017

number of pages

13

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inferred from page(s)

published in

Acta Neuropathologica

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14 October 2017

volume

67

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14 October 2017

issue

3-4

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14 October 2017

page(s)

177-189

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Juvenile dystonic lipidosis: An unusual form of neurovisceral storage disease

14 October 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00687799

The adrenoleukomyeloneuropathy complex: expression in four generations

21 January 2018

1 reference

12 December 2020

Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease

1 reference

12 December 2020

Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome

1 reference

12 December 2020

Fine structure of the cerebellum of children with lipidoses.

1 reference

12 December 2020

Pelizaeus-Merzbacher disease

1 reference

12 December 2020

A case of juvenile lipidosis: electron microscopic, histochemical and biochemical studies

1 reference

12 December 2020

1 reference

12 December 2020

Genetic contribution to the problem of the late form of Pelizaeus-Merzbacher disease

1 reference

12 December 2020

Cerebral demyelination associated with polycythemia vera.

1 reference

12 December 2020

Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome

1 reference

12 December 2020

Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy

1 reference

12 December 2020

Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes

1 reference

12 December 2020

Adrenomyeloneuropathy--clinical and biochemical diagnosis

1 reference

12 December 2020

Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies.

1 reference

12 December 2020

Specific involvement of muscle, nerve, and skin in late infantile and juvenile amaurotic idiocy

1 reference

12 December 2020

Cytoplasmic inclusions in juvenile amaurotic idiocy

1 reference

12 December 2020

[A familial syndrome with diffuse degenerative sclerosis (Pelizaeus-Merzbacher type), tapetoretinal degeneration & dwarfism; preliminary report]

1 reference

12 December 2020

ON THE DEGREE OF VARIATION IN PELIZAEUS-MERZBACHER DISEASE. (WITH A CONTRIBUTION TO FAMILIAL MULTIPLE SCLEROSIS)

1 reference

12 December 2020

Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis

1 reference

12 December 2020

Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study

1 reference

12 December 2020

Connatal Pelizaeus-Merzbacher Disease with congenital stridor in two maternal cousins

1 reference

12 December 2020

MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM

1 reference

12 December 2020

Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome

1 reference

12 December 2020

Fine structure of the myenteric plexus in various lipidoses

1 reference

12 December 2020

Fingerprint body myopathy, a newly recognized congenital muscle disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00687799

1 reference

14 October 2017

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