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Lista de obras de ELVIRAVALERIA DEMARCO

A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension

artículo científico publicado en 1999

A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.

artículo científico publicado en 2004

Alpha-synuclein promoter haplotypes and dementia in Parkinson's Disease

artículo científico publicado en 2008

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy

article

Association study between the LINGO1 gene and Parkinson's disease in the Italian population.

artículo científico publicado en 2011

Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene.

artículo científico publicado en 2004

Clinical Impact of OCT Findings During PCI: The CLI-OPCI II Study.

artículo científico publicado en 2015

Clinical Impact of Suboptimal Stenting and Residual Intrastent Plaque/Thrombus Protrusion in Patients With Acute Coronary Syndrome: The CLI-OPCI ACS Substudy (Centro per la Lotta Contro L'Infarto-Optimization of Percutaneous Coronary Intervention in

artículo científico publicado en 2016

Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism

article

DJ-1is a Parkinson's disease susceptibility gene in southern Italy

article

Enkephalin binding systems in human plasma. II: Leu-enkephalin serum albumin interaction

Enkephalin-binding systems in human plasma

artículo científico publicado en 1983

Gene dosage influences the age at onset of SCA2 in a family from southern Italy

artículo científico publicado en 2007

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

artículo científico publicado en 2006

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.

artículo científico publicado en 2008

Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant

artículo científico publicado en 1991

Hb J-Wenchang-Wuming or alpha 11(A9)Lys-->Gln in an Italian woman

scientific article published on 01 September 1995

Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease

article

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

artículo científico publicado en 2009

Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.

artículo científico publicado en 2011

Myocardial (123)I-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD.

artículo científico publicado en 2009

NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy

article

Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease

artículo científico publicado en 2010

Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease.

artículo científico publicado en 2013

SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases

artículo científico publicado en 2007

Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study

article

Spinocerebellar Ataxia Type 7: Report of a New Italian Family

article

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

artículo científico publicado en 2003

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