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Hearing Research
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April 7, 2025
Middle-aged CBA/CaJ mice exhibit auditory dysfunction in background noise
E Fabrizio-Stover, J Wu, H Lang, et al.
La Medicina Del Lavoro
|
November 1, 1995
[Relationship between exposure to environmental toxins and motor neuron disease: a case report]
N Vanacore, L Corsi, E Fabrizio, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 1, 1995
Familial Parkinson's disease: a clinical genetic analysis
V Bonifati, E Fabrizio, N Vanacore, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 19, 2001
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
V Bonifati, C B Lücking, E Fabrizio, et al.
Clinical Neuropharmacology
|
March 30, 2005
Levetiracetam in L-dopa-induced dyskinesia
G Meco, E Fabrizio, A Epifanio, et al.
Journal of Neurology
|
July 5, 2001
Frontal lobe dysfunction in essential tremor: a preliminary study
M Gasparini, V Bonifati, E Fabrizio, et al.
Nature Genetics
|
March 21, 1998
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Diseases of Aquatic Organisms
|
May 7, 2026
Detection of Anguillicoloides crassus (Nematoda) and a survey of endohelminths of American eels in Georgia, USA
Maggie A Young, Makala E Fabrizio, Vasyl V Tkach, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
V Bonifati, G De Michele, C B Lücking, et al.
Annals of Neurology
|
August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease
J Vaughan, A Durr, J Tassin, et al.
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Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Hearing Research
|
April 7, 2025
Middle-aged CBA/CaJ mice exhibit auditory dysfunction in background noise
E Fabrizio-Stover, J Wu, H Lang, et al.
La Medicina Del Lavoro
|
November 1, 1995
[Relationship between exposure to environmental toxins and motor neuron disease: a case report]
N Vanacore, L Corsi, E Fabrizio, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 1, 1995
Familial Parkinson's disease: a clinical genetic analysis
V Bonifati, E Fabrizio, N Vanacore, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 19, 2001
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
V Bonifati, C B Lücking, E Fabrizio, et al.
Clinical Neuropharmacology
|
March 30, 2005
Levetiracetam in L-dopa-induced dyskinesia
G Meco, E Fabrizio, A Epifanio, et al.
Journal of Neurology
|
July 5, 2001
Frontal lobe dysfunction in essential tremor: a preliminary study
M Gasparini, V Bonifati, E Fabrizio, et al.
Nature Genetics
|
March 21, 1998
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Diseases of Aquatic Organisms
|
May 7, 2026
Detection of Anguillicoloides crassus (Nematoda) and a survey of endohelminths of American eels in Georgia, USA
Maggie A Young, Makala E Fabrizio, Vasyl V Tkach, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
V Bonifati, G De Michele, C B Lücking, et al.
Annals of Neurology
|
August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease
J Vaughan, A Durr, J Tassin, et al.
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