6 Einträge gefunden

1. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

   1. Yilmaz, Rüstem
   2. Müller, Kathrin
   3. Brenner, David
   4. Volk, Alexander E
   5. Borck, Guntram
   6. Hermann, Andreas
   7. Meitinger, Thomas

   2020 - Forschungsinformationssystem des UKE
2. Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase

   1. Oeckl, Patrick
   2. Weydt, Patrick
   3. Steinacker, Petra
   4. Anderl-Straub, Sarah
   5. Nordin, Frida
   6. Volk, Alexander E
   7. Diehl-Schmid, Janine

   2019 - Forschungsinformationssystem des UKE
3. Phenotype in an Infant with SOD1 Homozygous Truncating Mutation

   1. Andersen, Peter M
   2. Nordström, Ulrika
   3. Tsiakas, Konstantinos
   4. Johannsen, Jessika
   5. Volk, Alexander E
   6. Bierhals, Tatjana
   7. Zetterström, Per

   2019 - Forschungsinformationssystem des UKE
4. Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis

   1. Volk, Alexander E
   2. Weishaupt, Jochen H
   3. Andersen, Peter M
   4. Ludolph, Albert C
   5. Kubisch, Christian

   2018 - Forschungsinformationssystem des UKE
5. Neurofilaments levels as biomarkers in asymptomatic and symptomatic familial ALS

   1. Weydt, Patrick
   2. Oeckl, Patrick
   3. Huss, André
   4. Müller, Kathrin
   5. Volk, Alexander E
   6. Kuhle, Jens
   7. Knehr, Antje

   2016 - Forschungsinformationssystem des UKE
6. Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

   1. Müller, Kathrin
   2. Andersen, Peter M
   3. Hübers, Annemarie
   4. Marroquin, Nicolai
   5. Volk, Alexander E
   6. Danzer, Karin M
   7. Meitinger, Thomas

   2014 - Forschungsinformationssystem des UKE