(Q37087350)

18 August 2017

Progressive cerebral poliodystrophy--Alpers' disease. Disorganized giant neuronal mitochondria on electron microscopy (English)

1 reference

18 August 2017

1 reference

1 reference

Sandbank U

1

1 reference

PMCID

494177

18 August 2017

Lerman P

series ordinal

2

1 reference

PMCID

494177

18 August 2017

language of work or name

English

0 references

publication date

1 December 1972

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

18 August 2017

1 reference

18 August 2017

35

1 reference

18 August 2017

6

1 reference

18 August 2017

749-755

1 reference

SOME BASIC PRINCIPLES OF "MOLECULAR PATHOLOGY". 3. ULTRACELLULAR ORGANELLES AS STRUCTURAL--METABOLIC AND PATHOGENETIC GRADIENTS

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Familial Progressive Poliodystrophy with Cirrhosis of the Liver

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Familial spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease). An ultrastructural study.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Giant neuronal mitochondria in a infant with microcephaly and seizure disorder

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Progressive degeneration of the cerebral cortex in infancy

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Spongy glio-neuronal dystrophy in infancy and childhood

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

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.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Electron microscopic changes in brain tissue of Syrian hamsters following acute hypoxia

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

PROGRESSIVE POLIODYSTROPHY. THE DEGENERATIONS OF CEREBRAL GRAY MATTER

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

THE SYNDROME OF PROGRESSIVE CEREBRAL POLIODYSTROPHY.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Progessive cerebral degeneration of infancy.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=494177

Fine structure of spongy degeneration of the central nervous system (van Bogaert and Bertrand type)

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4647849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A STUDY OF CHROMATOLYSIS IN DORSAL ROOT GANGLIA AT THE CELLULAR LEVEL

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4647849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial Myopathy With Abnormal Muscle Mitochondria

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4647849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.35.6.749

1 reference

18 August 2017

1 reference

18 August 2017

1 reference

PMCID

494177