E-LIB Suche - Ergebnisse für: Lange, Lara M.

1

Genetics and Pathogenesis of Dystonia:

Thomsen, Mirja ; Lange, Lara M. ; Zech, Michael.
Annual Review of Pathology: Mechanisms of Disease. 19 (2024) 1 - p. 99-131 , 2024

Link: https://doi.org/10.1146/..

2

MDSGene: Extending the List of Isolated Dystonia Genes by V..:

Thomsen, Mirja ; Lange, Lara M. ; Klein, Christine.
Movement Disorders. 38 (2023) 3 - p. 507-508 , 2023

Link: https://doi.org/10.1002/..

3

Elucidating causative gene variants in hereditary Parkinson..:

Lange, Lara M. ; Avenali, Micol ; Ellis, Melina...
npj Parkinson's Disease. 9 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

4

Author Correction: Elucidating causative gene variants in h..:

Lange, Lara M. ; Avenali, Micol ; Ellis, Melina...
npj Parkinson's Disease. 9 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

5

Nomenclature of Genetic Movement Disorders: Recommendations..:

Lange, Lara M. ; Gonzalez‐Latapi, Paulina ; Rajalingam, Rajasumi...
Movement Disorders. 37 (2022) 5 - p. 905-935 , 2022

Link: https://doi.org/10.1002/..

6

Atypical Parkinsonism with Pathological Dopamine Transporte..:

Lange, Lara M. ; Schell, Nathalie ; Tunc, Sinem...
Movement Disorders Clinical Practice. 9 (2022) 8 - p. 1116-1119 , 2022

Link: https://doi.org/10.1002/..

7

Genotype–Phenotype Relations for Isolated Dystonia Genes: M..:

Lange, Lara M. ; Junker, Johanna ; Loens, Sebastian...
Movement Disorders. 36 (2021) 5 - p. 1086-1103 , 2021

Link: https://doi.org/10.1002/..

8

A novel, in‐frame KMT2B deletion in a patient with apparent..:

Lange, Lara M. ; Tunc, Sinem ; Tennstedt, Stephanie...
Movement Disorders. 32 (2017) 10 - p. 1495-1497 , 2017

Link: https://doi.org/10.1002/..

9

Elucidating causative gene variants in hereditary Parkinson..:

Lange, Lara M ; Avenali, Micol ; Ellis, Melina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300084/. , 2023

Link: http://www.ncbi.nlm.nih...

10

Author Correction: Elucidating causative gene variants in h..:

Lange, Lara M ; Avenali, Micol ; Ellis, Melina...
https://boris.unibe.ch/189661/. , 2023

Link: https://boris.unibe.ch/1..

11

Elucidating causative gene variants in hereditary Parkinson..:

Lange, Lara M ; Avenali, Micol ; Solle, Justin...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41531-023-00526-9. , 2023

Link: https://pub.dzne.de/reco..

12

Nomenclature of Genetic Movement Disorders:Recommendations ..:

Lange, Lara M ; Gonzalez-Latapi, Paulina ; Rajalingam, Rajasumi...
https://research.rug.nl/en/publications/fda9aea2-a46d-4fd3-bb70-05b0aca492ff. , 2022

Link: https://hdl.handle.net/1..

13

Polyunsaturated fatty acids in the treatment of attention d..:

Lange, Klaus W. ; Hauser, Joachim ; Kanaya, Shigehiko...
Functional Foods in Health and Disease. 4 (2014) 6 - p. 245 , 2014

Link: https://doi.org/10.31989..

14

Circadian rhythms in obsessive–compulsive disorder:

Lange, Klaus W. ; Lange, Katharina M. ; Hauser, Joachim..
Journal of Neural Transmission. 119 (2012) 10 - p. 1077-1083 , 2012

Link: https://doi.org/10.1007/..

15

Polyunsaturated fatty acids in the treatment of attention d..:

Lange, Klaus W ; Hauser, Joachim ; Kanaya, Shigehiko...
https://research.rug.nl/en/publications/2aa51ade-68bd-4687-8025-9d0fc59a733c. , 2014

Link: https://hdl.handle.net/1..