About: José Félix Martí Massó

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

researcher ORCID ID = 0000-0001-8428-4386

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) researcher ORCID ID = 0000-0001-8428-4386 (en)
rdfs:label	José Félix Martí Massó (en) José Félix Martí Massó (es) José Félix Martí Massó (nl) José Félix Martí Massó (ast)
skos:prefLabel	José Félix Martí Massó (en) José Félix Martí Massó (es) José Félix Martí Massó (nl) José Félix Martí Massó (ast)
name	José Félix Martí Massó (en) José Félix Martí Massó (es) José Félix Martí Massó (nl) José Félix Martí Massó (ast)
given name	wds:Q59546069-30BF262B-2C51-4ED3-BC64-E1B63A76794D
given name	José
instance of	wds:Q59546069-6F6A8508-B04B-4561-991B-77CB4CD0C1BB
instance of	Homo sapiens
ResearchGate profile ID	wds:Q59546069-F8862072-70A5-499B-9601-F1F91FC17336
Semantic Scholar author ID	wds:Q59546069-84A94D21-E4AA-4746-AD91-E5FA43147EF2
ResearchGate profile ID	Jose_Marti-Masso
Semantic Scholar author ID	117260179
Google Scholar author ID	wds:Q59546069-42D7DCE1-9D28-4350-B388-302FD5E9B18D
Google Scholar author ID	a-22k-AAAAAJ
skos:altLabel	J F Marti Masso (en) Jose Felix Marti Masso (en)
Portuguese National Library author ID	wds:Q59546069-BC52290C-994D-4963-992E-2C85B7EBD660
occupation	wds:Q59546069-22CCC7C0-BA7D-42D0-9889-F1E898F33CF9
employer	wds:Q59546069-86CFF458-0CAE-4E57-8398-F523C3CCA768 wds:Q59546069-B571B83B-D408-4394-B8C5-212D196B6163
sex or gender	wds:Q59546069-BF0962E2-BC3F-4B6E-ADBC-197BEABD1851
VIAF ID	wds:Q59546069-d79d5a66-e5cf-46c4-aee6-b51d964960cc
country of citizenship	wds:Q59546069-1E24EDFE-2B5F-4E12-A776-0CCD28053C91
date of birth	wds:Q59546069-258cef8c-41ad-7a92-50b7-4b7128eadfd2
educated at	wds:Q59546069-bb065bf5-40a6-5400-e9bb-b4d3fb99a5b2
National Library of Spain ID	wds:Q59546069-B1420F5A-F664-4CFD-8F7C-9D206A7107F2
VIAF ID	http://viaf.org/viaf/170662377
National Library of Spain ID	http://datos.bne.es/resource/XX871684
Portuguese National Library author ID	1463244
occupation	researcher
employer	University of the Basque Country Donostia Hospital
sex or gender	male
VIAF ID	170662377
country of citizenship	Spain
date of birth	1947-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Navarre
National Library of Spain ID	XX871684
ORCID iD	wds:Q59546069-95F004E6-0684-48D5-8300-150DADF7426D
ORCID iD	https://orcid.org/0000-0001-8428-4386
ORCID iD	0000-0001-8428-4386
ResearcherID	wds:Q59546069-E64246F0-93F5-4C5F-A625-EE83923DFC5B
Publons author ID	wds:Q59546069-BB74E2AE-CBD4-4DDE-9096-2B9DBAF79C14
ResearcherID	D-8619-2013
Publons author ID	600951
is owl:sameAs of	José Félix Martí Massó José Félix Martí Massó
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59546069 https://es.wikipedia.org/wiki/Jos%C3%A9_F%C3%A9lix_Mart%C3%AD_Mass%C3%B3
is author of	Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1. Anticipation in myotonic dystrophy: a parental-sex-related phenomenon LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene. Acute Dystonia Induced by Sulpiride Generalized chorea induced by nonketotic hyperglycemia Creation of an open-access, mutation-defined fibroblast resource for neurological disease research Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis. A report of 50 cases. Nocturnal akathisia in Parkinson's disease: treatment with clozapine. Frequency of myotonic dystrophy gene carriers in cataract patients. Early treatment of Parkinson's disease with cabergoline delays the onset of motor complications. Results of a double-blind levodopa controlled trial. The PKDS009 Study Group. Phenotypic variability in familial prion diseases due to the D178N mutation. Cabergoline in the treatment of early Parkinson's disease: results of the first year of treatment in a double-blind comparison of cabergoline and levodopa. The PKDS009 Collaborative Study Group. Prevalence of Parkinson's disease and other types of Parkinsonism. A door-to-door survey in Bidasoa, Spain Somatosensory evoked potentials: abnormalities with focal brain lesions remote from the primary sensorimotor area The effect of visual cues on the number and duration of freezing episodes in Parkinson's patients. "Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation. Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain). The validity of Hodkinson's Abbreviated Mental Test for dementia screening in Guipuzcoa, Spain Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings. Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers. Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers. LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity. Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis Neurogenetic disorders in the Basque population Antibodies to Borrelia burgdorferi in Guillain-Barré syndrome Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. Prevalence of essential tremor: a door-to-door survey in bidasoa, spain Clinical signs of brain death simulated by Guillain-Barré syndrome [Autoimmune hepatitis in a patient with multiple sclerosis under treatment with glatiramer acetate] Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

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