(Q51246913)

English

Infantile neuroaxonal dystrophy. (Seitelberger's disease). Report of an autopsy case.

scientific article published in October 1965

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

Infantile neuroaxonal dystrophy. (Seitelberger's disease). Report of an autopsy case. (English)

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

1 reference

based on heuristic

inferred from title

author name string

Y Takei

1

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

publication date

1 October 1965

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

Acta Neuropathologica

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

5

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

1

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

1-15

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

https://scigraph.springernature.com/pub.10.1007/bf00689158

0 references

Infantile neuroaxonal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Late infantile form of Hallervorden-Spatz disease. II. Histochemical findings; discussion on nosology]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seitelberger's spastic amaurotic axonal idiocy. Report of a case in a 9-year-old boy with comment on visceral manifestations

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INFANTILE NEURO-AXONAL DEGENERATION (SEITELBERGER'S DISEASE). ANATOMICAL STUDY OF A CASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CONTRIBUTION TO LATE INFANTILE HALLERVORDEN-SPATZ DISEASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Late infantile form of the Hallervorden-Spatz disease. I. Clinical and anatomical findings]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degenerative encephalopathy of childhood (cortical degeneration, cerebellar atrophy, cholesterinosis of basal ganglia).

1 reference

https://pubmed.ncbi.nlm.nih.gov/5886195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00689158

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

1 reference

Europe PubMed Central

2 April 2018

http://europepmc.org/abstract/MED/5886195

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q51246913&oldid=1385797762"