Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Filter bei nächster Suche beibehalten
publishDate:"[2010 TO 2019]"
topic_facet:"genetics"
format_facet:"Aufsätze"
journalStr:"Movement disorders : official journal of the Movement Disorder Society"
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?filter%5B%5D=publishDate%3A%22%5B2010+TO+2019%5D%22&filter%5B%5D=topic_facet%3A%22genetics%22&filter%5B%5D=format_facet%3A%22Aufs%C3%A4tze%22&filter%5B%5D=journalStr%3A%22Movement+disorders+%3A+official+journal+of+the+Movement+Disorder+Society%22&type=AllFields
/vufind/Search/Results?filter%5B%5D=publishDate%3A%22%5B2010+TO+2019%5D%22&filter%5B%5D=topic_facet%3A%22genetics%22&filter%5B%5D=format_facet%3A%22Aufs%C3%A4tze%22&filter%5B%5D=journalStr%3A%22Movement+disorders+%3A+official+journal+of+the+Movement+Disorder+Society%22&type=AllFields
Search /vufind/Search2/Results?filter%5B%5D=publishDate%3A%22%5B2010+TO+2019%5D%22&filter%5B%5D=topic_facet%3A%22genetics%22&filter%5B%5D=format_facet%3A%22Aufs%C3%A4tze%22&filter%5B%5D=journalStr%3A%22Movement+disorders+%3A+official+journal+of+the+Movement+Disorder+Society%22&type=AllFields
PubPharm (43)
1
Twenty years on : Myoclonus-dystonia and ε-sarcoglycan - neurodevelopment, channel, and signaling dysfunction
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Menozzi, E.
|
Balint, B.
|
Latorre, A.
| +3
Wird geladen...
2
Nomenclature of Genetically Determined Myoclonus Syndromes : Recommendations of the International Parkinson and Movement Disorder Society Task Force
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
van der Veen, S.
|
Zutt, R.
|
Klein, C.
| +6
Wird geladen...
3
Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Heckman, M.
|
Kasanuki, K.
|
Brennan, R.
| +7
Wird geladen...
4
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Jabbari, E.
|
Woodside, J.
|
Tan, M.
| +12
Wird geladen...
5
SNCA Rep1 promoter variability influences cognition in Parkinson's disease
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Ng, A.
|
Tan, Y.
|
Zhao, Y.
| +11
Wird geladen...
6
Emerging links between pediatric lysosomal storage diseases and adult parkinsonism
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Ysselstein, D.
|
Shulman, J.
|
Krainc, D.
Wird geladen...
7
A clinical and genetic study of early-onset and familial parkinsonism in taiwan : An integrated approach combining gene dosage analysis and next-generation sequencing
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Lin, C.
|
Chen, P.
|
Tai, C.
| +4
Wird geladen...
8
SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Alcalay, R.
|
Mallett, V.
|
Vanderperre, B.
| +31
Wird geladen...
9
Sample enrichment for clinical trials to show delay of onset in huntington disease
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2019
von
Paulsen, J.
|
Lourens, S.
|
Kieburtz, K.
| +1
Wird geladen...
10
Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35 : MDSGene systematic review
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2018
von
Trinh, J.
|
Zeldenrust, F.
|
Huang, J.
| +11
Wird geladen...
1
2
3
4
5
Nächster »
[5]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Ihre gewählten Filter
Filter bei nächster Suche beibehalten
Filter aufheben
Alle gewählten Filter entfernen
Filter aufheben
Erscheinungsjahr: 2010-2019
Filter aufheben
Thema: genetics
Filter aufheben
Medienart: Aufsätze
Filter aufheben
Zeitschrift: Movement disorders : official journal of the Movement Disorder Society
Medienart
Aufsätze
43
E-Artikel
43
E-Ressourcen
Zeitschriftentitel
Movement disorders : official journal of the Mo...
Thema
genetics
41
Journal Article
33
Research Support, Non-U.S. Gov't
19
Parkinson's disease
12
Research Support, N.I.H., Extramural
9
Review
7
EC 2.7.11.1
5
LRRK2 protein, human
5
Leucine-Rich Repeat Serine-Threonine Protein Ki...
5
alpha-Synuclein
5
dystonia
5
parkinsonism
4
Protein Serine-Threonine Kinases
4
movement disorders
3
EC 2.3.2.27
3
EC 3.2.1.45
3
Glucosylceramidase
3
LRRK2
3
Molecular Chaperones
3
SNCA protein, human
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
2010-2019
9
2019
8
2018
4
2017
7
2016
7
2015
3
2014
5
2013
Alle anzeigen ...
weniger ...
Erscheinungsjahr(e)
Von:
Bis:
Sprache
43
Englisch
Haven't found what you're looking for?
Wird geladen...