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- Hagel, Christian
- Friedrich, Reinhard E 29
- Friedrich, Reinhard 25
- Glatzel, Markus 19
- Mautner, Victor-Felix 17
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176 Einträge gefunden
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Susceptibility to cellular stress in PS1 mutant N2a cells is associated with mitochondrial defects and altered calcium homeostasis
- Rojas-Charry, Liliana
- Calero-Martinez, Sergio
- Morganti, Claudia
- Morciano, Giampaolo
- Park, Kyungeun
- Hagel, Christian
- Marciniak, Stefan J
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Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis
- Farschtschi, Said C
- Kluwe, Lan
- Schön, Gerhard
- Friedrich, Reinhard E
- Matschke, Jakob
- Glatzel, Markus
- Hagel, Christian
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Contribution of mTOR and PTEN to Radioresistance in Sporadic and NF2-Associated Vestibular Schwannomas: A Microarray and Pathway Analysis
- Gugel, Isabel
- Ebner, Florian H
- Grimm, Florian
- Czemmel, Stefan
- Paulsen, Frank
- Hagel, Christian
- Tatagiba, Marcos
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Gorlin-Goltz-Syndrom (Nävoid-Basalzellkarzinom)
2020 - Forschungsinformationssystem des UKE -
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Lingual Mandibular Bone Depression
- Friedrich, Reinhard
- Barsukov, Evgeny
- Kohlrusch, Felix K
- Zustin, Josef
- Hagel, Christian
- Speth, Ulrike
- Vollkommer, Tobias
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Neurofibromatoses Typ 1 (NF1)
2020 - Forschungsinformationssystem des UKE -
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Differentiation of peripheral nerve sheath tumors in patients with neurofibromatosis type 1 using diffusion-weighted magnetic resonance imaging
- Well, Lennart
- Salamon, Johannes M
- Kaul, Michael G
- Farschtschi, Said
- Herrmann, Jochen
- Geier, Karin I
- Hagel, Christian
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Mice deficient in the lysosomal enzyme palmitoyl-protein thioesterase 1 (PPT1) display a complex retinal phenotype
- Atiskova, Yevgeniya
- Bartsch, Susanne
- Danyukova, Tatyana
- Becker, Elke
- Hagel, Christian
- Storch, Stephan
- Bartsch, Udo
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Driver mutations in USP8 wild type Cushing's disease
- Sbiera, Silviu
- Perez-Rivas, Luis Gustavo
- Taranets, Lyudmyla
- Weigand, Isabel
- Flitsch, Jörg
- Graf, Elisabeth
- Monoranu, Camelia-Maria
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Early-onset stroke in two siblings with Neurofibromatosis type 1
- Rukavina, Katarina
- Töpper, Rudolf
- Kunze, Alexandra
- Hess, Alexander
- Glatzel, Markus
- Valdueza, Jose Manuel
- Farschtschi, Said
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Repair of Occipital Bone Defects in Neurofibromatosis Type 1 by Means of CAD/CAM Prefabricated Titanium Plates
2018 - Forschungsinformationssystem des UKE -
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Autophagic vacuolar myopathy is a common feature in CLN3 disease
2018 - Forschungsinformationssystem des UKE -
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Surgical Treatment for Neonatal Hydrocephalus: Catheter-Based Cerebrospinal Fluid Diversion or Endoscopic Intervention?
2018 - Forschungsinformationssystem des UKE - frei zugänglich -
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Pigmented (melanotic) diffuse neurofibroma of the back in neurofibromatosis type 1
2018 - Forschungsinformationssystem des UKE - frei zugänglich