9 Einträge gefunden

1. Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study

   1. Rosenbohm, Angela
   2. Pott, Hendrik
   3. Thomsen, Mirja
   4. Rafehi, Haloom
   5. Kaya, Sabine
   6. Szymczak, Silke
   7. Volk, Alexander E

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
2. Different CSF protein profiles in amyotrophic lateral sclerosis and frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

   1. Barschke, Peggy
   2. Öckl, Patrick
   3. Steinacker, Petra
   4. Al Shweiki, Mhd Rami
   5. Weishaupt, Jochen H
   6. Landwehrmeyer, G Bernhard
   7. Anderl-Straub, Sarah

   2020 - Forschungsinformationssystem des UKE
3. Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis

   1. Verde, Federico
   2. Steinacker, Petra
   3. Weishaupt, Jochen H
   4. Kassubek, Jan
   5. Oeckl, Patrick
   6. Halbgebauer, Steffen
   7. Tumani, Hayrettin

   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. Poly-GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD

   1. Lehmer, Carina
   2. Oeckl, Patrick
   3. Weishaupt, Jochen H
   4. Volk, Alexander E
   5. Diehl-Schmid, Janine
   6. Schroeter, Matthias L
   7. Lauer, Martin

   2017 - Forschungsinformationssystem des UKE - frei zugänglich
6. The role of de novo mutations in the development of amyotrophic lateral sclerosis

   1. van Doormaal, Perry Tc
   2. Ticozzi, Nicola
   3. Weishaupt, Jochen H
   4. Kenna, Kevin
   5. Diekstra, Frank P
   6. Verde, Federico
   7. Andersen, Peter M

   2017 - Forschungsinformationssystem des UKE
7. 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
8. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients

   1. Hübers, Annemarie
   2. Just, Walter
   3. Rosenbohm, Angela
   4. Müller, Kathrin
   5. Marroquin, Nicolai
   6. Goebel, Ingrid
   7. Högel, Josef

   2015 - Forschungsinformationssystem des UKE
9. 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