6 Einträge gefunden

1. Patterns of synaptic loss in human amyotrophic lateral sclerosis spinal cord: a clinicopathological study

   1. Aousji, Oumayma
   2. Feldengut, Simone
   3. Antonucci, Stefano
   4. Schön, Michael
   5. Boeckers, Tobias M
   6. Matschke, Jakob
   7. Mawrin, Christian

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
2. 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
3. Neurofilament light chain as a blood biomarker to differentiate psychiatric disorders from behavioural variant frontotemporal dementia

   1. Al Shweiki, Mhd Rami
   2. Steinacker, Petra
   3. Oeckl, Patrick
   4. Hengerer, Bastian
   5. Danek, Adrian
   6. Fassbender, Klaus
   7. Diehl-Schmid, Janine

   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. 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
6. A complex form of hereditary spastic paraplegia in three siblings due to somatic mosaicism for a novel SPAST mutation in the mother

   1. Aulitzky, Anna
   2. Friedrich, Katrin
   3. Gläser, Dieter
   4. Gastl, Regina
   5. Kubisch, Christian
   6. Ludolph, Albert C
   7. Volk, Alexander

   2014 - Forschungsinformationssystem des UKE