(Q71272053)

English

Familial juvenile glio-neural dystrophy. Acutely beginning progressive encephalopathy with right-side occipitol-parietal focal symptoms and status epilepticus

scientific article published on 01 January 1969

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

Famili�re juvenile glio-neurale Dystrophie (German)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

10.1007/BF00341587

https://api.crossref.org/works/10.1007/BF00341587

8 May 2023

Familial juvenile glio-neural dystrophy. Acutely beginning progressive encephalopathy with right-side occipitol-parietal focal symptoms and status epilepticus (English)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5364610

8 May 2023

status epilepticus

1 reference

based on heuristic

inferred from title

author name string

H. Klein

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5364610

8 May 2023

J. Dichgans

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5364610

8 May 2023

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5364610

8 May 2023

publication date

1 January 1969

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00341587.pdf

Portable Document Format

1 reference

10.1007/BF00341587

https://api.crossref.org/works/10.1007/BF00341587

8 May 2023

http://link.springer.com/article/10.1007/BF00341587/fulltext.html

1 reference

10.1007/BF00341587

https://api.crossref.org/works/10.1007/BF00341587

8 May 2023

http://link.springer.com/content/pdf/10.1007/BF00341587

1 reference

10.1007/BF00341587

https://api.crossref.org/works/10.1007/BF00341587

8 May 2023

Archiv fur Psychiatrie und Nervenkrankheiten

212

4

400–22

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5364610

8 May 2023

212

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

400-422

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

Subacute spongiform encephalopathy--a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy).

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diffuse cerebral degeneration in infancy (Alpers' disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presenile glial dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Poliodysplasia cerebri

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute familial infantile heredodegenerative disorder of the central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial degeneration of the cerebral gray matter in childhood with convulsions, myoclonus, spasticity, cerebellar ataxia, choreoathetosis, dementia, and death in status epilepticus; differentiation of infantile and juvenile types

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progessive cerebral degeneration of infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE SYNDROME OF PROGRESSIVE CEREBRAL POLIODYSTROPHY.

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Illusions of comparative interpretation and emotion; production by epileptic discharge and by electrical stimulation in the temporal cortex.

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PROGRESSIVE POLIODYSTROPHY. THE DEGENERATIONS OF CEREBRAL GRAY MATTER

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive degeneration of the cerebral cortex in infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive subcortical gliosis, a rare form of presenile dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On general histopathology of degenerative processes of the nervous system]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etiology and pathogenesis of laminar cortical necrosis; its significance in evaluation of uniform cortical atrophies of early life

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Edematous disease of the central nervous system in early childhood]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Poliodystrophia cerebri progressiva, report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/5364610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DIFFUSE PROGRESSIVE DEGENERATION OF THE GRAY MATTER OF THE CEREBRUM

1

1 reference

10.1007/BF00341587

https://api.crossref.org/works/10.1007/BF00341587

8 May 2023

Identifiers

10.1007/BF00341587

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5364610%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

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