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Medientyp
- Text 9
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Erscheinungsjahr
Autor/in
- Weishaupt, Jochen H
- Volk, Alexander E 5
- Andersen, Peter M 4
- Marroquin, Nicolai 3
- Müller, Kathrin 3
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Sprache
- Englisch 9
9 Einträge gefunden
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Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study
- Rosenbohm, Angela
- Pott, Hendrik
- Thomsen, Mirja
- Rafehi, Haloom
- Kaya, Sabine
- Szymczak, Silke
- Volk, Alexander E
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Different CSF protein profiles in amyotrophic lateral sclerosis and frontotemporal dementia with C9orf72 hexanucleotide repeat expansion
- Barschke, Peggy
- Öckl, Patrick
- Steinacker, Petra
- Al Shweiki, Mhd Rami
- Weishaupt, Jochen H
- Landwehrmeyer, G Bernhard
- Anderl-Straub, Sarah
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Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
- Verde, Federico
- Steinacker, Petra
- Weishaupt, Jochen H
- Kassubek, Jan
- Oeckl, Patrick
- Halbgebauer, Steffen
- Tumani, Hayrettin
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Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis
2018 - Forschungsinformationssystem des UKE -
The role of de novo mutations in the development of amyotrophic lateral sclerosis
- van Doormaal, Perry Tc
- Ticozzi, Nicola
- Weishaupt, Jochen H
- Kenna, Kevin
- Diekstra, Frank P
- Verde, Federico
- Andersen, Peter M
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Poly-GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD
- Lehmer, Carina
- Oeckl, Patrick
- Weishaupt, Jochen H
- Volk, Alexander E
- Diehl-Schmid, Janine
- Schroeter, Matthias L
- Lauer, Martin
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Neurofilaments levels as biomarkers in asymptomatic and symptomatic familial ALS
- Weydt, Patrick
- Oeckl, Patrick
- Huss, André
- Müller, Kathrin
- Volk, Alexander E
- Kuhle, Jens
- Knehr, Antje
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De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- Hübers, Annemarie
- Just, Walter
- Rosenbohm, Angela
- Müller, Kathrin
- Marroquin, Nicolai
- Goebel, Ingrid
- Högel, Josef
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