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Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome

Journal of clinical oncology, 1998-07, Vol.16 (7), p.2478-2485

1998

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Further evidence for a somatic KRAS mutation in a pilocytic astrocytoma

Neuropediatrics, 2007-04, Vol.38 (2), p.61-63

2007

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Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort

The lancet oncology, 2018-06, Vol.19 (6), p.785-798

2018

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New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs

Cell, 2016-02, Vol.164 (5), p.1060-1072

2016

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Targeted therapeutics in treatment of children and young adults with solid tumors: an expert survey and review of the literature

Klinische Padiatrie, 2012-04, Vol.224 (3), p.124-131

2012

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Neonatal mastocytosis with pachydermic bullous skin without c-Kit 816 mutation

Dermatology (Basel), 2006-01, Vol.212 (1), p.70-72

2006

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Scheinbare Hyperchromasie und Makrozytose von Erythrozyten als technisches Artefakt bei Kältehämagglutininen

Monatsschrift für Kinderheilkunde, 1996, Vol.144 (5), p.537-539

SCHEURLEN, W

1996

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A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer

The EMBO journal, 1984-05, Vol.3 (5), p.1151-1157

1984

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Risk stratification in medulloblastoma: screening for molecular markers

Klinische Pädiatrie, 2006-05, Vol.218 (3), p.139-142

2006

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Chronic autoimmune thrombopenia/neutropenia in a boy with persistent parvovirus B19 infection

Journal of clinical virology, 2001-02, Vol.20 (3), p.173-178

2001

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Pulmonary Involvement in Pediatric-Onset Multisystem Langerhans Cell Histiocytosis: Effect on Course and Outcome

The Journal of pediatrics, 2012-07, Vol.161 (1), p.129-133.e3

2012

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Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics

Cytogenetic and genome research, 2000-01, Vol.90 (1-2), p.86-92

2000

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A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer

The EMBO journal, 1984-05, Vol.3 (5), p.1151-1157

1984

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Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea

Human mutation, 2001-09, Vol.18 (3), p.233-242

2001

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NO ABERRANT METHYLATION OF NEUROFIBROMATOSIS 1 GENE (NF1) PROMOTER IN PILOCYTIC ASTROCYTOMA IN CHILDHOOD

Pediatric hematology and oncology, 2005, Vol.22 (1), p.83-87

2005

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Analysis of the gap‐related domain of the neurofibromatosis type 1 (NF1) gene in childhood brain tumors

International journal of cancer, 1995-08, Vol.64 (4), p.234-238

1995

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Screening molekularbiologischer Marker zur Risikostratifizierung bei Medulloblastomen

Klinische Pädiatrie, 2006-05, Vol.218 (3), p.139-142

2006

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Foamy virus vectors for suicide gene therapy

Gene therapy, 1997-11, Vol.4 (11), p.1270-1277

1997

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DMBT1 , a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours

Nature genetics, 1997-09, Vol.17 (1), p.32-39

1997

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Agranulozytose bei einem 15 Monate alten Mädchen: Angeborene Neutropenie oder zyklische Neutropenie

Monatsschrift Kinderheilkunde, 1999-11, Vol.147 (11), p.1018-1022

1999

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Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

Genes chromosomes & cancer, 1999-07, Vol.25 (3), p.230-240

1999

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No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma

International journal of cancer, 1995-11, Vol.63 (3), p.372-374

1995

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Secondary malignant neoplasms after intensive treatment of relapsed acute lymphoblastic leukaemia in childhood

European journal of cancer (1990), 2008-01, Vol.44 (2), p.257-268

2008

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High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2

Genes chromosomes & cancer, 1997-01, Vol.18 (1), p.50-58

1997

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Spontaneous hematological remission in a boy with myelodysplastic syndrome and monosomy 7

Leukemia, 1994-08, Vol.8 (8), p.1435-1438

1994

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Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome

Further evidence for a somatic KRAS mutation in a pilocytic astrocytoma

Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort

New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs

Targeted therapeutics in treatment of children and young adults with solid tumors: an expert survey and review of the literature

Neonatal mastocytosis with pachydermic bullous skin without c-Kit 816 mutation

Scheinbare Hyperchromasie und Makrozytose von Erythrozyten als technisches Artefakt bei Kältehämagglutininen

A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer

Risk stratification in medulloblastoma: screening for molecular markers

Chronic autoimmune thrombopenia/neutropenia in a boy with persistent parvovirus B19 infection

Pulmonary Involvement in Pediatric-Onset Multisystem Langerhans Cell Histiocytosis: Effect on Course and Outcome

Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics

A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer

Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea

NO ABERRANT METHYLATION OF NEUROFIBROMATOSIS 1 GENE (NF1) PROMOTER IN PILOCYTIC ASTROCYTOMA IN CHILDHOOD

Analysis of the gap‐related domain of the neurofibromatosis type 1 (NF1) gene in childhood brain tumors

Screening molekularbiologischer Marker zur Risikostratifizierung bei Medulloblastomen

Foamy virus vectors for suicide gene therapy

DMBT1 , a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours

Agranulozytose bei einem 15 Monate alten Mädchen: Angeborene Neutropenie oder zyklische Neutropenie

Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma

Secondary malignant neoplasms after intensive treatment of relapsed acute lymphoblastic leukaemia in childhood

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2

Spontaneous hematological remission in a boy with myelodysplastic syndrome and monosomy 7

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