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- Text 9
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Autor/in
- Andersen, Peter M
- Volk, Alexander E 6
- Weishaupt, Jochen H 4
- Ludolph, Albert C 3
- Müller, Kathrin 3
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Sprache
- Englisch 9
9 Einträge gefunden
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SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden
- Yilmaz, Rüstem
- Müller, Kathrin
- Brenner, David
- Volk, Alexander E
- Borck, Guntram
- Hermann, Andreas
- Meitinger, Thomas
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Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population
- Korner, Sonja
- Kammeyer, Johanna
- Zapf, Antonia
- Kuzma-Kozakiewicz, Magdalena
- Piotrkiewicz, Maria
- Kuraszkiewicz, Bożenna
- Goszczynska, Hanna
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Phenotype in an Infant with SOD1 Homozygous Truncating Mutation
- Andersen, Peter M
- Nordström, Ulrika
- Tsiakas, Konstantinos
- Johannsen, Jessika
- Volk, Alexander E
- Bierhals, Tatjana
- Zetterström, Per
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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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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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