(Q48396810)

English

Congenital Pick cell encephalopathy: a distinct disorder characterized by diffuse formation of Pick cells in the cerebral cortex.

scientific article published in January 1986

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

Congenital Pick cell encephalopathy: a distinct disorder characterized by diffuse formation of Pick cells in the cerebral cortex. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

author name string

G A de León

1

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

G Breningstall

2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

N Zaeri

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

publication date

1 January 1986

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

70

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

3-4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

235-242

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

https://scigraph.springernature.com/pub.10.1007/bf00686077

0 references

Morbus Alzheimer and morbus Pick; a genetic, clinical and patho-anatomical study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Globoid cells, glial nodules, and peculiar fibrillary changes in the cerebro-hepato-renal syndrome of zellweger

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anatomical lesions of the Pick's disease in pre-atrophic phase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic cerebellar hypoplasia: a specific form of infantile spinal atrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Separating Pena-Shokeir I syndrome from the "arthrogryposis basket"

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An ultrastructural study of Pick bodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Periventricular leukomalacia of infancy. A form of neonatal anoxic encephalopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classic and generalized variants of Pick's disease: A clinicopathological, ultrastructural, and immunocytochemical comparative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histological and ultrastructural features of dystrophic isocortical axons in infantile neuroaxonal dystrophy (Seitelberger's disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new case of Pick's disease. Anatomical and ultrastructural studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anterior horn cell disease associated with pontocerebellar hypoplasia in infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia: a pathologic analysis of one infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine structure of the Pick and Hirano bodies in a case of Pick's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pick's disease. A clinical and ultrastructural study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile Pick's disease: clinical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic degeneration of the telencephalic subependymal germinal layer in newborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3766124

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00686077

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/3766124

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=Q48396810&oldid=1383739166"