About: Ingeborg Krägeloh-Mann

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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
description	forskare (sv) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) জার্মান গবেষক (bn) հետազոտող (hy) ഗവേഷകന്‍ (ml) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) ikertzaile alemaniarra (eu) chercheuse allemande (fr) investigadora alemana (es) investigadora alemana (ast) investigadora alemanya (ca) investigadora alemá (gl) investigadora alemã (pt) Wissenschaftlerin, Präsidentin der Deutschen Gesellschaft für Kinder- und Jugendmedizin (de)
rdfs:label	Ingeborg Krägeloh-Mann (ca) Ingeborg Krägeloh-Mann (de) Ingeborg Krägeloh-Mann (en) Ingeborg Krägeloh-Mann (es) Ingeborg Krägeloh-Mann (nl) Ingeborg Krägeloh-Mann (sl) Ingeborg Krägeloh-Mann (ast)
skos:prefLabel	Ingeborg Krägeloh-Mann (ca) Ingeborg Krägeloh-Mann (de) Ingeborg Krägeloh-Mann (en) Ingeborg Krägeloh-Mann (es) Ingeborg Krägeloh-Mann (nl) Ingeborg Krägeloh-Mann (sl) Ingeborg Krägeloh-Mann (ast)
name	Ingeborg Krägeloh-Mann (ca) Ingeborg Krägeloh-Mann (de) Ingeborg Krägeloh-Mann (en) Ingeborg Krägeloh-Mann (es) Ingeborg Krägeloh-Mann (nl) Ingeborg Krägeloh-Mann (sl) Ingeborg Krägeloh-Mann (ast)
given name	wds:Q21261811-67CDC001-316A-4249-9D42-47810EBCF2D5
given name	Ingeborg
instance of	wds:Q21261811-265CD0E3-2B19-41A5-91DC-F8E33A455785
instance of	Homo sapiens
Loop ID	wds:Q21261811-7d29a5b3-42a3-1060-454c-a486837f0310
Loop ID	19723
occupation	wds:Q21261811-9B717AD9-3245-4E58-8715-947B33A42072
NSK ID	wds:Q21261811-3c2919e7-44a8-1823-b7de-1c8116a2ceb8
languages spoken, written or signed	wds:Q21261811-4B1445AF-999A-4876-B4D4-8561754C64E7
sex or gender	wds:Q21261811-41354F48-BC8B-4FA8-8E1E-8D0B167D7121
VIAF ID	wds:Q21261811-1683335D-E1A0-44D1-942A-3AB51B0AB64E
GND ID	wds:Q21261811-8b863580-401d-f66d-1199-918d4e8e617d
country of citizenship	wds:Q21261811-eb148f85-450c-793d-83a7-6d7c9a19faa4
WorldCat Identities ID (superseded)	wds:Q21261811-8647BC59-8348-4F84-BA45-BF18A3F07ACD
VIAF ID	http://viaf.org/viaf/305782629
GND ID	https://d-nb.info/gnd/1109928335
occupation	researcher
NSK ID	000598992
languages spoken, written or signed	German
sex or gender	female organism
VIAF ID	305782629
GND ID	1109928335
country of citizenship	Germany
WorldCat Identities ID (superseded)	viaf-305782629
ORCID iD	wds:Q21261811-FBADC73B-90DA-4733-8525-72310A2BE1DE
ORCID iD	https://orcid.org/0000-0003-4599-1373
ORCID iD	0000-0003-4599-1373
AcademiaNet ID	wds:Q21261811-FF66573D-0CB4-46B7-9FCE-03225FECA902
AcademiaNet ID	1173794
is owl:sameAs of	Ingeborg Krägeloh-Mann
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q21261811
is author of	Perception and production of biological movement in patients with early periventricular brain lesions Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Biological motion processing in adolescents with early periventricular brain damage. Perception and understanding of others' actions and brain connectivity. tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia Reorganization in congenital hemiparesis acquired at different gestational ages Misleading functional magnetic resonance imaging mapping of the cortical hand representation in a 4-year-old boy with an arteriovenous malformation of the central region Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy The natural course of gross motor deterioration in metachromatic leukodystrophy Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course. Two types of ipsilateral reorganization in congenital hemiparesis: a TMS and fMRI study The role of magnetic resonance imaging in elucidating the pathogenesis of cerebral palsy: a systematic review European consensus table 2006 on botulinum toxin for children with cerebral palsy Brain representation of active and passive hand movements in children. Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant. Cerebral palsy update Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate Global and local development of gray and white matter volume in normal children and adolescents

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