11 Einträge gefunden

1. Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome

   1. Niehues, Tim
   2. Özgür, Tuba Turul
   3. Bickes, Marie
   4. Waldmann, Rebecca
   5. Schöning, Jennifer
   6. Bräsen, Jan
   7. Hagel, Christian

   2020 - Forschungsinformationssystem des UKE
2. Lack of astrocytes hinders parenchymal oligodendrocyte precursor cells from reaching a myelinating state in osmolyte-induced demyelination

   1. Lohrberg, Melanie
   2. Winkler, Anne
   3. Franz, Jonas
   4. van der Meer, Franziska
   5. Ruhwedel, Torben
   6. Sirmpilatze, Nikoloz
   7. Dadarwal, Rakshit

   2020 - Forschungsinformationssystem des UKE
3. C-Fiber Loss as a Possible Cause of Neuropathic Pain in Schwannomatosis

   1. Farschtschi, Said C
   2. Mainka, Tina
   3. Glatzel, Markus
   4. Hannekum, Anna-Lena
   5. Hauck, Michael
   6. Gelderblom, Mathias
   7. Hagel, Christian

   2020 - Forschungsinformationssystem des UKE
4. Susceptibility to cellular stress in PS1 mutant N2a cells is associated with mitochondrial defects and altered calcium homeostasis

   1. Rojas-Charry, Liliana
   2. Calero-Martinez, Sergio
   3. Morganti, Claudia
   4. Morciano, Giampaolo
   5. Park, Kyungeun
   6. Hagel, Christian
   7. Marciniak, Stefan J

   2020 - Forschungsinformationssystem des UKE
5. Lingual Mandibular Bone Depression

   1. Friedrich, Reinhard
   2. Barsukov, Evgeny
   3. Kohlrusch, Felix K
   4. Zustin, Josef
   5. Hagel, Christian
   6. Speth, Ulrike
   7. Vollkommer, Tobias

   2020 - Forschungsinformationssystem des UKE
6. Contribution of mTOR and PTEN to Radioresistance in Sporadic and NF2-Associated Vestibular Schwannomas: A Microarray and Pathway Analysis

   1. Gugel, Isabel
   2. Ebner, Florian H
   3. Grimm, Florian
   4. Czemmel, Stefan
   5. Paulsen, Frank
   6. Hagel, Christian
   7. Tatagiba, Marcos

   2020 - Forschungsinformationssystem des UKE - frei zugänglich
7. Null phenotype of neurofibromatosis type 1 in a carrier of a heterozygous atypical NF1 deletion due to mosaicism

   1. Kluwe, Lan
   2. Friedrich, Reinhard E
   3. Farschtschi, Said C
   4. Hagel, Christian
   5. Kehrer-Sawatzki, Hildegard
   6. Mautner, Victor-Felix

   2020 - Forschungsinformationssystem des UKE
8. Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg

   1. Friedrich, Reinhard E
   2. Hagel, Christian
   3. Kohlrusch, Felix K
   4. Schanze, Ina
   5. Wieland, Ilse
   6. Zenker, Martin

   2020 - Forschungsinformationssystem des UKE
9. Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis

   1. Farschtschi, Said C
   2. Kluwe, Lan
   3. Schön, Gerhard
   4. Friedrich, Reinhard E
   5. Matschke, Jakob
   6. Glatzel, Markus
   7. Hagel, Christian

   2020 - Forschungsinformationssystem des UKE
10. Posterior fossa pilocytic astrocytomas with oligodendroglial features show frequent FGFR1 activation via fusion or mutation

    1. Sievers, Philipp
    2. Schrimpf, Daniel
    3. Stichel, Damian
    4. Reuss, David E
    5. Hasselblatt, Martin
    6. Hagel, Christian
    7. Staszewski, Ori

    2020 - Forschungsinformationssystem des UKE
11. Neuropathology of patients with COVID-19 in Germany: a post-mortem case series

    1. Matschke, Jakob
    2. Lütgehetmann, Marc
    3. Hagel, Christian
    4. Sperhake, Jan P
    5. Schröder, Ann Sophie
    6. Edler, Carolin
    7. Mushumba, Herbert

    2020 - Forschungsinformationssystem des UKE