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Diagnostic criteria and genetics of the PEHO syndrome
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
title
Diagnostic criteria and genetics of the PEHO syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
main subject
PEHO syndrome
1 reference
based on heuristic
inferred from title
author name string
Somer M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 November 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
volume
30
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
page(s)
932-936
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
cites work
Hereditary diseases in Finland; rare flora in rare soul
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
21 June 2018
Variation of growth in height and weight of children. II. After infancy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
21 June 2018
Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
21 June 2018
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
21 June 2018
Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
30 October 2018
PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy): neuroradiologic findings.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016602
retrieved
30 October 2018
Identifiers
DOI
10.1136/JMG.30.11.932
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
PMCID
1016602
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
PubMed ID
8301648
1 reference
stated in
Europe PubMed Central
PubMed ID
8301648
retrieved
28 July 2017
ResearchGate publication ID
14896947
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