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Contribution of mTOR and PTEN to Radioresistance in Sporadic and NF2-Associated Vestibular Schwannomas: A Microarray and Pathway Analysis
2020 - Forschungsinformationssystem des UKE - frei zugänglich
Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis
2020 - Forschungsinformationssystem des UKE
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome
2020 - Forschungsinformationssystem des UKE
Lingual Mandibular Bone Depression
2020 - Forschungsinformationssystem des UKE
C-Fiber Loss as a Possible Cause of Neuropathic Pain in Schwannomatosis
2020 - Forschungsinformationssystem des UKE
Null phenotype of neurofibromatosis type 1 in a carrier of a heterozygous atypical NF1 deletion due to mosaicism
2020 - Forschungsinformationssystem des UKE
Neurofibromatoses Typ 2 (NF2)
2020 - Forschungsinformationssystem des UKE
Neurofibromatoses Typ 1 (NF1)
2020 - Forschungsinformationssystem des UKE
Susceptibility to cellular stress in PS1 mutant N2a cells is associated with mitochondrial defects and altered calcium homeostasis
2020 - Forschungsinformationssystem des UKE
Lack of astrocytes hinders parenchymal oligodendrocyte precursor cells from reaching a myelinating state in osmolyte-induced demyelination
2020 - Forschungsinformationssystem des UKE
Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg
2020 - Forschungsinformationssystem des UKE
Normale Entwicklung und Fehlbildungen des Nervensystems
1. Hagel, Christian
2. Panteliadis, Christos
2020 - Forschungsinformationssystem des UKE
Posterior fossa pilocytic astrocytomas with oligodendroglial features show frequent FGFR1 activation via fusion or mutation
2020 - Forschungsinformationssystem des UKE
Gorlin-Goltz-Syndrom (Nävoid-Basalzellkarzinom)
2020 - Forschungsinformationssystem des UKE
Neuropathology of patients with COVID-19 in Germany: a post-mortem case series
2020 - Forschungsinformationssystem des UKE

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Contribution of mTOR and PTEN to Radioresistance in Sporadic and NF2-Associated Vestibular Schwannomas: A Microarray and Pathway Analysis

Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis

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

Lingual Mandibular Bone Depression

C-Fiber Loss as a Possible Cause of Neuropathic Pain in Schwannomatosis

Null phenotype of neurofibromatosis type 1 in a carrier of a heterozygous atypical NF1 deletion due to mosaicism

Neurofibromatoses Typ 2 (NF2)

Neurofibromatoses Typ 1 (NF1)

Susceptibility to cellular stress in PS1 mutant N2a cells is associated with mitochondrial defects and altered calcium homeostasis

Lack of astrocytes hinders parenchymal oligodendrocyte precursor cells from reaching a myelinating state in osmolyte-induced demyelination

Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg

Normale Entwicklung und Fehlbildungen des Nervensystems

Posterior fossa pilocytic astrocytomas with oligodendroglial features show frequent FGFR1 activation via fusion or mutation

Gorlin-Goltz-Syndrom (Nävoid-Basalzellkarzinom)

Neuropathology of patients with COVID-19 in Germany: a post-mortem case series