4 Einträge gefunden

1. AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance

   1. Lang-Roth, Ruth
   2. Fischer-Krall, Eva
   3. Kornblum, Cornelia
   4. Nürnberg, Gudrun
   5. Meschede, Dieter
   6. Goebel, Ingrid
   7. Nürnberg, Peter

   2017 - Forschungsinformationssystem des UKE
2. A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction

   1. Fazeli, Walid
   2. Herkenrath, Peter
   3. Stiller, Barbara
   4. Neugebauer, Antje
   5. Fricke, Julia
   6. Lang-Roth, Ruth
   7. Nürnberg, Gudrun

   2017 - Forschungsinformationssystem des UKE
3. The rapid evolution of molecular genetic diagnostics in neuromuscular diseases

   1. Volk, Alexander E
   2. Kubisch, Christian

   2017 - Forschungsinformationssystem des UKE
4. 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