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journalStr:"Movement disorders : official journal of the Movement Disorder Society"
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PubPharm (15)
1
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2024
von
Ojo, O.
|
Bandres-Ciga, S.
|
Makarious, M.
| +110
UpdateOf: medRxiv. 2023 Nov 09;:. - PMID 38076854
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2
SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2024
von
Rudaks, L.
|
Yeow, D.
|
Kumar, K.
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3
Dystonia Linked to EIF4A2 Haploinsufficiency : A Disorder of Protein Translation Dysfunction
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2023
von
Harrer, P.
|
Škorvánek, M.
|
Kittke, V.
| +25
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4
Underrepresented Populations in Parkinson's Genetics Research : Current Landscape and Future Directions
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Schumacher-Schuh, A.
|
Bieger, A.
|
Okunoye, O.
| +119
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5
Harnessing Transcriptomics to Decipher Dystonia Pathogenesis
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Fellner, A.
|
Kumar, K.
CommentOn: Am J Hum Genet. 2021 Nov 4;108(11):2145-2158. - PMID 34672987
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6
Nomenclature of Genetic Movement Disorders : Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Lange, L.
|
Gonzalez-Latapi, P.
|
Rajalingam, R.
| +15
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7
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb Involvement
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Zech, M.
|
Kumar, K.
|
Reining, S.
| +26
CommentIn: Mov Disord. 2022 May;37(5):1113-1115. - PMID 35587627
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8
New gene implicated in early-onset generalized dystonia : Lysine-specific methyltransferase 2B (KMT2B)
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2017
von
Siow, S.
|
Kumar, K.
CommentOn: Am J Hum Genet. 2016 Dec 1;99(6):1377-1387. - PMID 27839873
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9
Mutations in TUBB4A and spastic paraplegia
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2015
von
Kumar, K.
|
Vulinovic, F.
|
Lohmann, K.
| +4
CommentOn: Mov Disord. 2015 May;30(6):854-8. - PMID 25772097
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10
ADCY5 identified as a novel cause of benign hereditary chorea
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2015
von
Raj Kumar, K.
|
Fung, V.
CommentOn: Neurology. 2015 Jul 7;85(1):80-8. - PMID 26085604
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Zeitschrift: Movement disorders : official journal of the Movement Disorder Society
Medienart
15
Aufsätze
15
E-Artikel
15
E-Ressourcen
Zeitschriftentitel
Movement disorders : official journal of the Mo...
Thema
11
Journal Article
9
Research Support, Non-U.S. Gov't
7
Comment
4
Review
4
genetics
2
EC 3.2.1.45
2
Editorial
2
Glucosylceramidase
2
Letter
2
Parkinson's disease
2
loss-of-function variants
1
149223-81-4
1
94ZLA3W45F
1
ADCY5
1
AOPEP
1
AOPEP protein, human
1
Adenylyl Cyclases
1
Aminopeptidases
1
Anti-Dyskinesia Agents
1
Arginine
Alle anzeigen ...
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Erscheinungszeitraum
7
2020-
8
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
15
Englisch
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