About: Gabriele Siciliano

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

Italian neurologist

Attributes	Values
rdf:type	Item
description	연구원 (ko) গবেষক (bn) 研究者 (ja) wetenschapper (nl) дослідник (uk) 研究者 (zh) հետազոտող (hy) İtalyan bilim insanı (tr) Italian neurologist (en) neurólogo italiano (es) طبيب أعصاب إيطالي (ar) neurologo italiano (it)
rdfs:label	Gabriele Siciliano (en) Gabriele Siciliano (es) Gabriele Siciliano (it) Gabriele Siciliano (nl) Gabriele Siciliano (sl) Gabriele Siciliano (ast)
skos:prefLabel	Gabriele Siciliano (en) Gabriele Siciliano (es) Gabriele Siciliano (it) Gabriele Siciliano (nl) Gabriele Siciliano (sl) Gabriele Siciliano (ast)
name	Gabriele Siciliano (en) Gabriele Siciliano (es) Gabriele Siciliano (it) Gabriele Siciliano (nl) Gabriele Siciliano (sl) Gabriele Siciliano (ast)
given name	wds:Q42143936-977EC724-44BE-472E-9D89-C526B988F4E8
given name	Gabriele
instance of	wds:Q42143936-B73C6BFD-78ED-4EA3-9D6E-48BE432BC835
instance of	Homo sapiens
Loop ID	wds:Q42143936-E5D4698F-8CDF-4E2F-A8EF-80D5530E0F0F
Loop ID	209741
Semantic Scholar author ID	wds:Q42143936-2BDFBE31-A889-4C40-AB15-40CEE9FC8E19
Semantic Scholar author ID	2695319
occupation	wds:Q42143936-1D52CB09-2055-4F6F-B79E-C586DAB85BE3
employer	wds:Q42143936-2818F3ED-6CDD-49F8-B7AF-49BAAB88609B
languages spoken, written or signed	wds:Q42143936-7fcb1a87-4da4-b52f-8d6b-bfb9f22ad930
sex or gender	wds:Q42143936-D464292E-03B1-403B-946C-6651826B3F11
country of citizenship	wds:Q42143936-e09f5d4c-4bf7-bdec-e310-81c3b2de7313
educated at	wds:Q42143936-92d0e8f8-4f64-8218-23e2-3c4222c6040e
family name	wds:Q42143936-2086CECB-340A-4ED7-AC4C-FC072E934336
occupation	neurologist
employer	University of Pisa
languages spoken, written or signed	Italian
sex or gender	male
country of citizenship	Italy
educated at	University of Pisa
family name	Siciliano
ORCID iD	wds:Q42143936-82B17ABC-641D-40AA-9FF3-05E1D8F83746
ORCID iD	https://orcid.org/0000-0002-6142-2384
ORCID iD	0000-0002-6142-2384
IRIS UNIGE author ID	wds:Q42143936-57DB2464-D53F-41B5-B00D-1C4628B87A4E
IRIS UNIGE author ID	50664
ResearcherID	wds:Q42143936-77DBEAE2-F99B-4746-95CA-8020A8486E48
Publons author ID	wds:Q42143936-76705bf9-3178-449a-b87e-4095b2b95821
ResearcherID	K-7259-2016
Publons author ID	1200961
ARPI author ID	wds:Q42143936-8DD6B158-8689-4B5B-BC0C-A1592E3E8078
ARPI author ID	00072
Padua Research Archive author ID	wds:Q42143936-D400B609-89D9-4669-963B-50BDC6D4047F
Padua Research Archive author ID	32353
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42143936
is author of	APOE and Alzheimer disease: a major gene with semi-dominant inheritance Searching for the role and the most suitable biomarkers of oxidative stress in Alzheimer's disease and in other neurodegenerative diseases. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease Alzheimer's pathogenesis and its link to the mitochondrion Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy Human dental pulp stem cells protect mouse dopaminergic neurons against MPP+ or rotenone. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis Evaluation of cytogenetic and DNA damage in mitochondrial disease patients: effects of coenzyme Q10 therapy Oxcarbazepine is effective and safe in the treatment of neuropathic pain: pooled analysis of seven clinical studies Structural and functional evaluation of cortical motor areas in Amyotrophic Lateral Sclerosis. Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: Report of a family Novel sarcoglycan gene mutations in a large cohort of Italian patients. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study Mutations of FUS gene in sporadic amyotrophic lateral sclerosis Antimyoclonic effect of levetiracetam in MERRF syndrome Facioscapulohumeral Muscular Dystrophy Type 1A in Northwestern Tuscany: A Molecular Genetics-based Epidemiological and Genotype–Phenotype Study Causative and susceptibility genes for Alzheimer's disease: a review. Central nervous system involvement in Anderson-Fabry disease: a clinical and MRI retrospective study. Prognostic factors in mild dystrophinopathies Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathies Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeutics The hOGG1 Ser326Cys polymorphism is not associated with sporadic Parkinson's disease Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy. Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Oxidative DNA damage in peripheral leukocytes of mild cognitive impairment and AD patients Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosispatients Molecular diagnosis in LGMD2A: mutation analysis or protein testing? Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation Impaired oxidative metabolism and lipid peroxidation in exercising muscle from ALS patients A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

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