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journalStr:"Movement disorders : official journal of the Movement Disorder Society"
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PubPharm (4)
1
GBA-Related Parkinson's Disease : Dissection of Genotype-Phenotype Correlates in a Large Italian Cohort
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2020
von
Petrucci, S.
|
Ginevrino, M.
|
Trezzi, I.
| +64
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2
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2011
von
Criscuolo, C.
|
De Rosa, A.
|
Guacci, A.
| +8
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3
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2006
von
Criscuolo, C.
|
Volpe, G.
|
De Rosa, A.
| +8
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4
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2005
von
Criscuolo, C.
|
Saccà, F.
|
De Michele, G.
| +7
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1
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Zeitschrift: Movement disorders : official journal of the Movement Disorder Society
Medienart
4
Aufsätze
2
E-Artikel
2
E-Ressourcen
2
Gedruckte Aufsätze
Zeitschriftentitel
Movement disorders : official journal of the Mo...
Thema
4
Journal Article
4
Research Support, Non-U.S. Gov't
2
Case Reports
2
EC 2.7.11.1
1
Amino Acids
1
EC 2.7.-
1
EC 3.2.1.45
1
GBA
1
Glucosylceramidase
1
Heat-Shock Proteins
1
LRRK2 protein, human
1
Leucine-Rich Repeat Serine-Threonine Protein Ki...
1
PTEN-induced putative kinase
1
Parkinson's disease
1
Protein Kinases
1
Protein Serine-Threonine Kinases
1
SACS protein, human
1
dementia
1
genotype-phenotype correlates
1
impulsive-compulsive behavior
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