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15 Einträge gefunden

Neurofibromatoses Typ 1 (NF1)
2020 - Forschungsinformationssystem des UKE
Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis
2020 - Forschungsinformationssystem des UKE
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
Gorlin-Goltz-Syndrom (Nävoid-Basalzellkarzinom)
2020 - Forschungsinformationssystem des UKE
Posterior fossa pilocytic astrocytomas with oligodendroglial features show frequent FGFR1 activation via fusion or mutation
2020 - Forschungsinformationssystem des UKE
Neuropathology of patients with COVID-19 in Germany: a post-mortem case series
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
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
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome
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
Normale Entwicklung und Fehlbildungen des Nervensystems
1. Hagel, Christian
2. Panteliadis, Christos
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

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Neurofibromatoses Typ 1 (NF1)

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

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

Gorlin-Goltz-Syndrom (Nävoid-Basalzellkarzinom)

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

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

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

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

Neurofibromatoses Typ 2 (NF2)

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

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

Normale Entwicklung und Fehlbildungen des Nervensystems

Lingual Mandibular Bone Depression

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