(Q34432868)

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The PEHO syndrome

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 August 2017

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Europe PubMed Central

The PEHO syndrome (English)

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Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

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inferred from title

author name string

Riikonen R

1

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Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

1 November 2001

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Europe PubMed Central

PubMed publication ID

2 August 2017

Brain and Development

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Europe PubMed Central

PubMed publication ID

2 August 2017

23

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Europe PubMed Central

PubMed publication ID

2 August 2017

7

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Europe PubMed Central

PubMed publication ID

2 August 2017

765-769

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Diagnostic criteria and genetics of the PEHO syndrome

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in two Japanese siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

PEHO or PEHO-like syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Cerebellar hypoplasia in Werdnig-Hoffmann disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Cell death during development of the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Transient IGF-I gene expression during the maturation of functionally related central projection neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

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Survival of Purkinje Cells in Cerebellar Cultures is Increased by Insulin-like Growth Factor I.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Insulin-like growth factor-I modulation of cerebellar cell populations is developmentally stage-dependent and mediated by specific intracellular pathways.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

The insulin-like growth factor I system in cerebellar degeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Insulin-like growth factor I restores motor coordination in a rat model of cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Topical application of insulin like growth factor-1 reduces edema and upregulation of neuronal nitric oxide synthase following trauma to the rat spinal cord

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Low insulin-like growth factor (IGF-1) in the cerebrospinal fluid of children with progressive encephalopathy, hypsarrhythmia, and optic atrophy (PEHO) syndrome and cerebellar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Markedly elevated nitrate/nitrite levels in the cerebrospinal fluid of children with progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900283-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0387-7604(01)00283-2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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