about
A new family with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.Two sisters with familial dyskeratotic comedones.MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedemaSurvival data for 299 patients with primary cutaneous lymphomas: a monocentre study.CD56-positive haematological neoplasms of the skin: a multicentre study of the Cutaneous Lymphoma Project Group of the European Organisation for Research and Treatment of Cancer.Cytogenetic characterization of complex karyotypes in seven established melanoma cell lines by multiplex fluorescence in situ hybridization and DAPI banding.Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).A case of late-onset primary hyperoxaluria type 1.Symmetric nodules on both soles in a 4-month-old baby.Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations.Cytotoxic/natural killer cell cutaneous lymphomas. Report of EORTC Cutaneous Lymphoma Task Force Workshop.Simultaneous aberrations of single CDKN2A network components and a high Rb phosphorylation status can differentiate subgroups of primary cutaneous B-cell lymphomas.High frequency ofMYCgene amplification is a common feature of radiation-induced sarcomas. Further results from EORTC STBSG TL 01/01Granulomatous Mycosis Fungoides and Granulomatous Slack SkinCytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortionsRegulatory T-cell phenotype in association with large cell transformation of mycosis fungoidesNew prognostic relevant factors in primary cutaneous diffuse large B-cell lymphomasIs FOXP3 expressed in cutaneous T-cell lymphomas?Chromosomal aberration patterns differ in subtypes of primary cutaneous B cell lymphomasDistinct types of primary cutaneous large B-cell lymphoma identified by gene expression profilingNo chromosomal imbalances in seborrheic keratoses detectable by comparative genomic hybridization[Nodular erythema and B-symptoms]
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description
researcher, ORCID id # 0000-0003-1620-1723
@en
wetenschapper
@nl
name
Christian Hallermann
@ast
Christian Hallermann
@en
Christian Hallermann
@es
Christian Hallermann
@nl
type
label
Christian Hallermann
@ast
Christian Hallermann
@en
Christian Hallermann
@es
Christian Hallermann
@nl
prefLabel
Christian Hallermann
@ast
Christian Hallermann
@en
Christian Hallermann
@es
Christian Hallermann
@nl
P106
P21
P31
P496
0000-0003-1620-1723