E-LIB Suche - Ergebnisse für: Huber, Nadine

1

Rare PMP22 variants in mild to severe neuropathy uncorrelat..:

Palu, Edouard ; Järvilehto, Julius ; Pennonen, Jana...
neurogenetics. 24 (2023) 4 - p. 291-301 , 2023

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

2

Organotypic Hippocampal Slice Cultures from Adult Tauopathy..:

Kemppainen, Susanna ; Huber, Nadine ; Willman, Roosa-Maria...
Cells. 12 (2023) 10 - p. 1422 , 2023

Link: https://doi.org/10.3390/..

3

Cortico-spinal tDCS in amyotrophic lateral sclerosis: A ran..:

Benussi, Alberto ; Cantoni, Valentina ; Grassi, Mario...
Brain Stimulation. 16 (2023) 6 - p. 1666-1676 , 2023

Link: https://doi.org/10.1016/..

4

C9orf72 hexanucleotide repeat expansion leads to altered ne..:

Huber, Nadine ; Hoffmann, Dorit ; Giniatullina, Raisa...
Neurobiology of Disease. 162 (2022) - p. 105584 , 2022

Link: https://doi.org/10.1016/..

5

Neurofilament Light Regulates Axon Caliber, Synaptic Activi..:

Sainio, Markus T. ; Rasila, Tiina ; Molchanova, Svetlana M....
Frontiers in Cell and Developmental Biology. 9 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

6

Serum total TDP-43 levels are decreased in frontotemporal d..:

Katisko, Kasper ; Huber, Nadine ; Kokkola, Tarja...
Alzheimer's Research & Therapy. 14 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

7

Pneumonektomie mit schweren Folgen:

Huber, Nadine ; Opitz, Isabelle ; Schpbach, Reto.
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum. , 2022

Link: https://doi.org/10.4414/..

8

Threshold of heteroplasmic truncating MT-ATP6 mutation in r..:

Kenvin, Sebastian ; Torregrosa-Muñumer, Ruben ; Reidelbach, Marco...
Human Molecular Genetics. 31 (2021) 6 - p. 958-974 , 2021

Link: https://doi.org/10.1093/..

9

Serum GFAP and NfL levels in benign relapsing-remitting mul..:

Niiranen, Marja ; Kontkanen, Aleksi ; Jääskeläinen, Olli...
Multiple Sclerosis and Related Disorders. 56 (2021) - p. 103280 , 2021

Link: https://doi.org/10.1016/..

10

c-Jun N-terminal kinase 2 suppresses pancreatic cancer grow..:

Tian, Xiaodong ; Traub, Benno ; Shi, Jingwei...
Cancer Gene Therapy. 29 (2021) 1 - p. 73-86 , 2021

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

11

Expression of C9orf72 hexanucleotide repeat expansion leads..:

Leskelä, Stina ; Huber, Nadine ; Hoffmann, Dorit...
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1868 (2021) 7 - p. 119021 , 2021

Link: https://doi.org/10.1016/..

12

Deficient neurotransmitter systems and synaptic function in..:

Huber, Nadine ; Korhonen, Sonja ; Hoffmann, Dorit...
Molecular Psychiatry. 27 (2021) 3 - p. 1300-1309 , 2021

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

13

FTLD Patient–Derived Fibroblasts Show Defective Mitochondri..:

Leskelä, Stina ; Hoffmann, Dorit ; Rostalski, Hannah...
Molecular Neurobiology. 58 (2021) 11 - p. 5438-5458 , 2021

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

14

BV-2 Microglial Cells Overexpressing C9orf72 Hexanucleotide..:

Rostalski, Hannah ; Hietanen, Tomi ; Leskelä, Stina...
Frontiers in Neurology. 11 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

15

PSEN1ΔE9, APPswe, and APOE4 Confer Disparate Phenotypes in ..:

Konttinen, Henna ; Cabral-da-Silva, Mauricio e Castro ; Ohtonen, Sohvi...
Stem Cell Reports. 13 (2019) 4 - p. 669-683 , 2019

Link: https://doi.org/10.1016/..