About: Albert C. Ludolph

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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:Q75573197-24B0BF1E-1C31-41E9-AA46-4382DA9E03DA
field of work	neurology
description	ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh)
rdfs:label	Albert C Ludolph (nl) Albert C. Ludolph (cs) Albert C. Ludolph (de) Albert C. Ludolph (en) Albert C. Ludolph (sk)
skos:prefLabel	Albert C Ludolph (nl) Albert C. Ludolph (cs) Albert C. Ludolph (de) Albert C. Ludolph (en) Albert C. Ludolph (sk)
name	Albert C Ludolph (nl) Albert C. Ludolph (cs) Albert C. Ludolph (de) Albert C. Ludolph (en) Albert C. Ludolph (sk)
given name	wds:Q75573197-A2C9040F-513C-41CE-9D51-533A3E68F026
given name	Albert
instance of	wds:Q75573197-87B47EF1-062A-4D0E-8D83-405A908CEFE1
NL CR AUT ID	wds:Q75573197-32F0A516-7677-4D58-9AD8-DFAE44709049
instance of	Homo sapiens
NL CR AUT ID	xx0051299
skos:altLabel	Albert C Ludolph (en) Albert Christian Ludolph (cs) Albert Ludolph (en)
occupation	wds:Q75573197-d4bf3d92-4a78-967f-ed2b-076f447b38b6
sex or gender	wds:Q75573197-7D6D67D7-155E-419F-9F68-6541E3771C8D
ISNI	wds:Q75573197-92FE9B41-FE1E-4D7F-B6A9-BC79E74250C2
VIAF ID	wds:Q75573197-D54C3CCD-B0EC-4B30-9C7F-16F1739E886E
Library of Congress authority ID	wds:Q75573197-7EEF0407-6885-47F5-B4BB-93D95F904365
Bibliothèque nationale de France ID	wds:Q75573197-23836453-85CE-4A43-89FA-D1A6FEBF4891
IdRef ID	wds:Q75573197-E4475575-6AA2-4305-89F4-5DE51B4BC945
date of birth	wds:Q75573197-69F07995-0CCC-40EA-8E0C-B0C961AC4AEA
PLWABN ID	wds:Q75573197-CAD800F2-09E6-49E9-BC48-4490F1AC9D77
National Library of Israel J9U ID	wds:Q75573197-732D68E0-6643-47A5-8570-73EB88DF478A
VIAF ID	http://viaf.org/viaf/311118040
Library of Congress authority ID	http://id.loc.gov/authorities/names/no97020804
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb14507567x#about
IdRef ID	http://www.idref.fr/061444669/id
occupation	researcher
sex or gender	male
ISNI	000000011757798X
VIAF ID	311118040
Library of Congress authority ID	no97020804
Bibliothèque nationale de France ID	14507567x
IdRef ID	061444669
date of birth	1932-01-01 00:00:00Z (xsd:dateTime)
PLWABN ID	9810613432705606
National Library of Israel J9U ID	987007424147005171
ORCID iD	wds:Q75573197-D14A6892-1716-4FB5-9D84-43A14D42341C
ORCID iD	https://orcid.org/0000-0002-5401-0904
ORCID iD	0000-0002-5401-0904
is owl:sameAs of	Albert C. Ludolph
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q75573197
is author of	Tubulin-binding cofactor B is a direct interaction partner of the dynactin subunit p150(Glued) Mechanisms, models and biomarkers in amyotrophic lateral sclerosis Neuroimaging of motor neuron diseases Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel-based morphometry of 3-D MRI. Depression and quality of life in patients with amyotrophic lateral sclerosis Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal aging The economic costs of progressive supranuclear palsy and multiple system atrophy in France, Germany and the United Kingdom Neuroimaging of multimodal sensory stimulation in amyotrophic lateral sclerosis Brain responses to emotional stimuli in patients with amyotrophic lateral sclerosis (ALS). Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers Amygdala size in amyotrophic lateral sclerosis without dementia: an in vivo study using MRI volumetry Late-onset motoneuron disease caused by a functionally modified AMPA receptor subunit Emotional responding in amyotrophic lateral sclerosis. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic? Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues Quality of life in fatal disease: the flawed judgement of the social environment. Longitudinal effects of noninvasive positive-pressure ventilation in patients with amyotrophic lateral sclerosis. Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis. Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization. Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD. Comparison of longitudinal metabolite relaxation times in different regions of the human brain at 1.5 and 3 Tesla Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect Micronutrients supplementation and nutritional status in cognitively impaired elderly persons: a two-month open label pilot study PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis Adipose Tissue Distribution Predicts Survival in Amyotrophic Lateral Sclerosis High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: A prospective interventional study No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort. Glatiramer acetate has no impact on disease progression in ALS at 40 mg/day: a double- blind, randomized, multicentre, placebo-controlled trial IgG antibodies against measles, rubella, and varicella zoster virus predict conversion to multiple sclerosis in clinically isolated syndrome Proteome analysis reveals candidate markers of disease progression in amyotrophic lateral sclerosis (ALS). A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosis Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD). Amyotrophic lateral sclerosis--a model of corticofugal axonal spread

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