Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Schindler%2C+Alice%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Schindler%2C+Alice%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Schindler%2C+Alice%22&type=Person&sort=year
PubPharm (55)
1
A Heterozygous Mutation in MFF Associated with a Mild Mitochondrial Phenotype
enthalten in:
Journal of neuromuscular diseases
| 2023
von
Murata, D.
|
Grunseich, C.
|
Iijima, M.
| +6
Wird geladen...
2
Life-Long Steroid Responsive Familial Myopathy With Docking Protein 7 Mutation
enthalten in:
Journal of clinical neuromuscular disease
| 2022
von
Oh, S.
|
King, P.
|
Schindler, A.
Wird geladen...
3
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease
enthalten in:
Brain : a journal of neurology
| 2022
von
Zhu, W.
|
Huang, X.
|
Yoon, E.
| +13
Wird geladen...
4
Improving the efficacy of exome sequencing at a quaternary care referral centre : novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases
enthalten in:
Journal of neurology, neurosurgery, and psychiatry
| 2021
von
Grunseich, C.
|
Sarkar, N.
|
Lu, J.
| +15
Wird geladen...
5
α-Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's Disease
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2021
von
Isonaka, R.
|
Goldstein, D.
|
Zhu, W.
| +12
Wird geladen...
6
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease
enthalten in:
bioRxiv.org
| 2021
von
Zhu, W.
|
Huang, X.
|
Yoon, E.
| +12
Wird geladen...
7
α‐Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's Disease
enthalten in:
Movement Disorders
| 2021
von
Isonaka, R.
|
Goldstein, D.
|
Zhu, W.
| +12
Wird geladen...
8
Cardiac MRI identifies valvular and myocardial disease in a subset of ANO5-related muscular dystrophy patients
enthalten in:
Neuromuscular disorders : NMD
| 2020
von
Srinivasan, R.
|
Yun, P.
|
Neuhaus, S.
| +8
Wird geladen...
9
Author response : Peripheral synucleinopathy in a DJ1 patient with Parkinson disease, cataracts, and hearing loss
enthalten in:
Neurology
| 2020
von
Narendra, D.
|
Isonaka, R.
|
Nguyen, D.
| +7
CommentOn: Neurology. 2019 Jun 4;92(23):1113-1115. - PMID 31028127
Wird geladen...
10
Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4
enthalten in:
Annals of neurology
| 2020
von
Grunseich, C.
|
Patankar, A.
|
Amaya, J.
| +6
Wird geladen...
1
2
3
4
5
6
Nächster »
[6]
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
Medienart
55
Aufsätze
40
E-Artikel
40
E-Ressourcen
15
Gedruckte Aufsätze
Zeitschriftentitel
8
Annals of clinical and translational neurology
4
Journal of genetic counseling
4
Journal of neurology
4
Neuromuscular disorders : NMD
3
Annals of neurology
3
Neurology
2
Advances in experimental medicine and biology
2
American journal of human genetics
2
Human mutation
2
Journal of neuromuscular diseases
2
Muscle & nerve
2
Neuromuscular disorders
2
The lancet <London> / Neurology
1
Annals of Neurology
1
Brain : a journal of neurology
1
Case reports in neurology
1
Development (Cambridge, England)
1
Journal of clinical neuromuscular disease
1
Journal of clinical neuroscience
1
Journal of clinical neuroscience : official jou...
Alle anzeigen ...
weniger ...
Thema
35
Journal Article
12
Research Support, N.I.H., Intramural
8
Case Reports
8
Research Support, Non-U.S. Gov't
7
Research Support, N.I.H., Extramural
4
Genetic counseling
3
CMT
3
Charcot Marie Tooth disease
3
DNA Helicases
3
Demyelinating Neuropathy
3
EC 3.6.1.-
3
EC 3.6.4.-
3
EC 3.6.4.13
3
Ethical concerns
3
Genetic subtypes
3
Hereditary motor and sensory neuropathy
3
Lysosomal Storage Disease
3
Motor Neuron Disease
3
Multifunctional Enzymes
3
Psychosocial concerns
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
11
2020-
41
2010-2019
3
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
46
Englisch
Haven't found what you're looking for?
Wird geladen...