(Q48822813)

English

Neuroaxonal dystrophy with neuromelanin deposition, neurofibrillary tangles, and neuronal loss. Light- and electron-microscopic changes in a 45-year-old woman with progressive psychomotor deterioration.

scientific article published in January 1983

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

Neuroaxonal dystrophy with neuromelanin deposition, neurofibrillary tangles, and neuronal loss. Light- and electron-microscopic changes in a 45-year-old woman with progressive psychomotor deterioration. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

neuroaxonal dystrophy

1 reference

based on heuristic

inferred from title

author name string

H A Hartmann

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

S K White

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

R L Levine

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

publication date

1 January 1983

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

number of pages

4

1 reference

based on heuristic

inferred from page(s)

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

61

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

3-4

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

169-172

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

https://scigraph.springernature.com/pub.10.1007/bf00691981

0 references

Neuroaxonal dystrophy in young adults: a clinicopathological study of two unrelated cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinico-pathological and histochemical studies of Hallervorden-Spatz disease with torsion dystonia with special reference to diagnostic criteria of the disease from the clinico-pathological viewpoint.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The striatonigral degenerations. Putaminal pigments and nosology

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous pallido-nigral accumulation of iron pigment and spheroid-like structures in macaque monkeys.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis-dementia complex, neuroaxonal dystrophy, and Hallervorden-Spatz disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The chemistry of the brain / Leslie L. Iversen. - (9.1979)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hallervorden-Spatz syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroaxonal dystrophy (Seitelberger's disease) with late onset, protracted course and myoclonic epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructure of Hirano bodies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts).

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxomal dystrophy or Seitelberger's disease. Clinical, histological and ultrastructural study of 2 observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis of pigment and spheroid formation in Hallervorden-Spatz syndrome and related disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectroscopic studies of substantia nigra pigment in human subjects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6650130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00691981

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/6650130

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=Q48822813&oldid=1765338234"