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Parkinsonism & Related Disorders
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December 1, 2009
Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review
L Correia Guedes, J J Ferreira, M M Rosa, et al.
Acta Neurologica Scandinavica
|
July 1, 1995
Estimate of parkinsonism prevalence through drug prescription histories in the Province of Rome, Italy
F Menniti-Ippolito, S Spila-Alegiani, N Vanacore, et al.
Journal of Neurology
|
November 27, 2013
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
L Di Toro Mammarella, A Mignarri, C Battisti, et al.
Neurology
|
June 11, 2008
Re: LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
V Bonifati, Y-H Wu-Chou, D Schweiger, et al.
Neurology
|
January 12, 2007
Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease
S Goldwurm, M Zini, L Mariani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2003
Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [11C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2)
A Antonini, R M Moresco, C Gobbo, et al.
Neurology
|
November 26, 2003
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism
P Ibáñez, G De Michele, V Bonifati, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease
T Gasser, B Müller-Myhsok, A Supala, et al.
Acta Neurologica Scandinavica
|
May 1, 2001
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines
C Colosimo, N Vanacore, V Bonifati, 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.
Page
of 8
Search research articles
Search
Showing results (31-40 of 78) with videos related to
Sort By:
Page
of 8
Parkinsonism & Related Disorders
|
December 1, 2009
Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review
L Correia Guedes, J J Ferreira, M M Rosa, et al.
Acta Neurologica Scandinavica
|
July 1, 1995
Estimate of parkinsonism prevalence through drug prescription histories in the Province of Rome, Italy
F Menniti-Ippolito, S Spila-Alegiani, N Vanacore, et al.
Journal of Neurology
|
November 27, 2013
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
L Di Toro Mammarella, A Mignarri, C Battisti, et al.
Neurology
|
June 11, 2008
Re: LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
V Bonifati, Y-H Wu-Chou, D Schweiger, et al.
Neurology
|
January 12, 2007
Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease
S Goldwurm, M Zini, L Mariani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2003
Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [11C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2)
A Antonini, R M Moresco, C Gobbo, et al.
Neurology
|
November 26, 2003
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism
P Ibáñez, G De Michele, V Bonifati, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease
T Gasser, B Müller-Myhsok, A Supala, et al.
Acta Neurologica Scandinavica
|
May 1, 2001
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines
C Colosimo, N Vanacore, V Bonifati, 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.
Page
of 8