About: Rudolf Korinthenberg

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
field of work	wds:Q47702475-0EF789F1-B60E-4986-997D-AD044A8CAFBA wds:Q47702475-79EA7960-3035-4D18-A35F-4DF002EE5647 wds:Q47702475-CFA4DA73-A478-4954-BFEF-1AA56137E1E9
field of work	pediatrics medicine pediatric neurology
description	ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) wetenschapper (nl) дослідник (uk) 研究者 (zh) հետազոտող (hy) hulumtues (sq) taighdeoir (ga) lékař, univerzitní profesor; pediatr, dětský neurolog (cs)
rdfs:label	Rudolf Korinthenberg (cs) Rudolf Korinthenberg (en) Rudolf Korinthenberg (es) Rudolf Korinthenberg (nl) Rudolf Korinthenberg (sl) Rudolf Korinthenberg (sq) Rudolf Korinthenberg (ast)
skos:prefLabel	Rudolf Korinthenberg (cs) Rudolf Korinthenberg (en) Rudolf Korinthenberg (es) Rudolf Korinthenberg (nl) Rudolf Korinthenberg (sl) Rudolf Korinthenberg (sq) Rudolf Korinthenberg (ast)
name	Rudolf Korinthenberg (cs) Rudolf Korinthenberg (en) Rudolf Korinthenberg (es) Rudolf Korinthenberg (nl) Rudolf Korinthenberg (sl) Rudolf Korinthenberg (sq) Rudolf Korinthenberg (ast)
Scopus author ID	wds:Q47702475-70BD3B94-2E59-4155-9DA5-E883123A4C0E
Scopus author ID	7006730671
given name	wds:Q47702475-06122B70-E5E8-4536-84B7-8238F5ED3500
given name	Rudolf
instance of	wds:Q47702475-C56367D5-4395-4E30-B510-D665F6AFF33D
NL CR AUT ID	wds:Q47702475-362AF673-64F4-49D3-9BD7-CB3A84ECA0BB
instance of	Homo sapiens
NL CR AUT ID	xx0262508
occupation	wds:Q47702475-7156FFF3-92EC-41F9-85C8-4D8D4193DE1E wds:Q47702475-974ad90b-b699-49d3-bb42-1750afb6745d wds:Q47702475-e98e1540-70f0-4a13-9c0c-5b7c570bdadd wds:Q47702475-ff78b40d-08b2-40d9-a3b2-94208618534f
employer	wds:Q47702475-128739C5-ED1B-4FDF-B908-755306E52112 wds:Q47702475-44A2DED5-058D-496E-A655-31B41400AE06 wds:Q47702475-A8194B2C-2CB7-4EC7-B17A-1A0DC4334AB3
languages spoken, written or signed	wds:Q47702475-922358E2-67A1-4AC3-A0DC-AA6B688085EE wds:Q47702475-B367DADC-D5BA-46A9-A143-626F33B532E0
place of birth	wds:Q47702475-200BC36D-6C06-46DB-A9BE-70267A334BBB
sex or gender	wds:Q47702475-716F4367-5C0E-4783-AEAC-B6517305E6C1
ISNI	wds:Q47702475-E3A78A60-CF54-48BD-8BC3-455D94A392C4
VIAF ID	wds:Q47702475-EF0EC47C-69BA-45B1-8232-F6A17F7B4A8F
GND ID	wds:Q47702475-A94B94A6-C5C0-4DD6-9AF4-9A3B977FD1B5
Library of Congress authority ID	wds:Q47702475-DA0564F5-8A54-49D5-B86A-F76E6D52A23A
IdRef ID	wds:Q47702475-711414FC-4706-4304-A3B5-D308AA4F8079
date of birth	wds:Q47702475-C9081CB8-685E-45D0-955C-DEFD1154827D wds:Q47702475-E8BCFD1E-A068-4DBA-8725-5B98C23AACEA
educated at	wds:Q47702475-F794F31D-7472-477B-AE58-B422AFD909C4
WorldCat Identities ID (superseded)	wds:Q47702475-AA1631AB-8322-4738-862B-1EC324EC2943
VIAF ID	http://viaf.org/viaf/49509440
GND ID	https://d-nb.info/gnd/139234039
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2008183349
IdRef ID	http://www.idref.fr/094175411/id
occupation	university teacher neurologist physician pediatrician
employer	University of Freiburg Mannheim University Hospital University Hospital Muenster
languages spoken, written or signed	English German
place of birth	Düsseldorf
sex or gender	male
ISNI	0000000038636347
VIAF ID	49509440
GND ID	139234039
Library of Congress authority ID	n2008183349
IdRef ID	094175411
date of birth	1949-04-13 00:00:00Z (xsd:dateTime)
educated at	University Medical Center Freiburg
WorldCat Identities ID (superseded)	lccn-n2008183349
ORCID iD	wds:Q47702475-A78548D8-E86F-433D-A906-5FEABD38B52E
ORCID iD	https://orcid.org/0000-0002-4638-3460
ORCID iD	0000-0002-4638-3460
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47702475
is author of	Clinical characteristics in focal cortical dysplasia: a retrospective evaluation in a series of 120 patients. Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations Focal cortical dysplasia: a genotype-phenotype analysis of polymorphisms and mutations in the TSC genes. ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

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