(Q48354875)

English

Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).

scientific article published in January 1993

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

1 reference

based on heuristic

inferred from title

author name string

M Haltia

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

M Somer

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

publication date

1 January 1993

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

85

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

241-247

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

https://scigraph.springernature.com/pub.10.1007/bf00227717

0 references

Hereditary disease of the cerebellar parenchyma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar hypoplasia in Werdnig-Hoffmann disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathological aspects of infantile spasms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

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Cerebellar hypoplasia associated with systemic degeneration in early life

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early familial cerebellar degeneration; report of 3 cases in one family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

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/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onset

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cerebellar atrophy of the granular type]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the relationship between human and experimental granule cell type cerebellar degeneration.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

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A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary degeneration of the granular layer of the cerebellum (Norman type). A Golgi study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concordant primary atrophy of the cerebellar granules in monozygotic twins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

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inferred from PubMed ID database lookup

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar Hypoplasia in Werdnig-Hoffmann Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

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/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential roles of multiple adhesion molecules in cell migration: granule cell migration in cerebellum

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary atrophy of the granular layer of the cerebellum as described by R. M. Norman. Study of 2 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8460530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00227717

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/8460530

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