(Q41634403)

5 October 2017

title

Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins (English)

1 reference

5 October 2017

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

1 reference

Pelizaeus-Merzbacher disease

21 March 2024

main subject

congenital disorder

0 references

1 reference

W. O. Renier

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

F. J. Gabreëls

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

T. W. Hustinx

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

H. H. Jaspar

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

J. A. Geelen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

U. J. Van Haelst

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

E. J. Lommen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

B. G. Ter Haar

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7234326

21 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7234326

21 March 2024

publication date

1 January 1981

1 reference

full work available at URL

5 October 2017

http://link.springer.com/content/pdf/10.1007/BF00691328.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00691328/fulltext.html

21 March 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF00691328

21 March 2024

1 reference

21 March 2024

published in

Acta Neuropathologica

1 reference

5 October 2017

volume

54

1 reference

5 October 2017

issue

1

1 reference

5 October 2017

page(s)

11-17

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00691328

5 October 2017

exact match

0 references

cites work

[The mouse mutant "Jimpy". Animal model of leukodystrophy]

1 reference

12 December 2020

Pelizaeus-Merzbacher disease

1 reference

12 December 2020

Histochemical, ultrastructural and biochemical studies of a case with leukodystrophy due to congenital deficiency of myelin

1 reference

12 December 2020

Outcome in congenital stridor (laryngomalacia).

1 reference

12 December 2020

CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

1 reference

12 December 2020

Changes of the ratio between myelin thickness and axon diameter in the human developing sural nerve

1 reference

12 December 2020

Stridor in the first year of life. The clinical evaluation of the persistent or intermittent noisy breather

1 reference

12 December 2020

Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?

1 reference

12 December 2020

Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings

1 reference

12 December 2020

Congenital failure of myelinization: Pelizaeus-Merzbacher disease?

1 reference

12 December 2020

THE ASSESSMENT OF STRIDOR IN INFANTS AND YOUNG CHILDREN.

1 reference

12 December 2020

The infant with stridor; a follow-up survey of 80 cases

1 reference

12 December 2020

INTELLECTUAL IMPAIRMENT IN CONGENITAL LARYNGEAL STRIDOR

1 reference

12 December 2020

Changes in glial cells during human telencephalic myelinogenesis

1 reference

12 December 2020

Pelizacus-Merzbacher disease. Transitional form between classical and co-natal (Seitelberger) type.

1 reference

12 December 2020

[Combination of two old methods of histological study of the central nervous system]

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

Pelizaeusmerzbacher disease "infantile acute type"; report of a family

1 reference

12 December 2020

Familial laryngeal abductor paralysis and psychomotor retardation

1 reference

12 December 2020

Congenital retarded myelinization in a new-born child with infantile spasms

1 reference

12 December 2020

Concentration and fatty acid composition of cerebrosides and sulfatides in mature and immature human brain.

1 reference

12 December 2020

Pelizaeus-Metzbacher disease: clinical diagnosis

1 reference

12 December 2020

[Merzbacher-Pelizaeus disease; clinico-anatomic studies of its position among the diffuse scleroses]

1 reference

12 December 2020

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

1 reference

12 December 2020

Quantitative cytoarchitectonics of the human cerebral cortex

1 reference

12 December 2020

Dysmyelination Revisited

1 reference

12 December 2020

PELIZAEUS-MERZBACHER DISEASE. A STUDY IN NOSOLOGY

1 reference

12 December 2020

Fortschritte der Medizin

9

45

2623

C Meier

1977

1 reference

21 March 2024

Identifiers

DOI

10.1007/BF00691328

1 reference

5 October 2017

1 reference