UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)

Journal of Medical Genetics, 2014-05, Vol.51 (5), p.283-293

2014

Volltextzugriff (PDF)

Imaging Features with Histopathologic Correlation of CNS High-Grade Neuroepithelial Tumors with a BCOR Internal Tandem Duplication

American journal of neuroradiology : AJNR, 2022-01, Vol.43 (1), p.151-156

2022

Volltextzugriff (PDF)

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort

Journal of medical genetics, 2015-11, Vol.52 (11), p.770-778

2015

Volltextzugriff (PDF)

Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRI

American journal of neuroradiology : AJNR, 2020-09, Vol.41 (9), p.1733-1739

2020

Volltextzugriff (PDF)

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

Familial cancer, 2021-10, Vol.20 (4), p.305-316

2021

Volltextzugriff (PDF)

Malformations, genetic abnormalities, and wilms tumor

Pediatric blood & cancer, 2014-01, Vol.61 (1), p.140-144

2014

Volltextzugriff (PDF)

Indications and results of diagnostic biopsy in pediatric renal tumors: A retrospective analysis of 317 patients with critical review of SIOP guidelines

Pediatric blood & cancer, 2019-06, Vol.66 (6), p.e27641-n/a

2019

Volltextzugriff (PDF)

Silence would be the greatest error

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2015-08, Vol.22 (8), p.899-899

2015

Volltextzugriff (PDF)

Rhabdoid component emerging as a subclonal evolution of paediatric glioneuronal tumours

Neuropathology and applied neurobiology, 2018-02, Vol.44 (2), p.224-228

2018

Volltextzugriff (PDF)

In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin

Oncogene, 2008-05, Vol.27 (21), p.3066-3071

2008

Volltextzugriff (PDF)

Rhadboid tumours: hSNF/INI1 deficient cancers of early childhood with aggressive behaviour

Bulletin du cancer, 2010-01, Vol.97 (1), p.37

2010

Volltextzugriff (PDF)

Les émotions dans la relation de soin : des racines de leur répression aux enjeux de leur expression

Éthique & santé, 2006, Vol.3 (3), p.133-137

Bourdeaut, F.

2006

Volltextzugriff (PDF)

Prédispositions génétiques en oncologie pédiatrique

Oncologie (Paris, France), 2016-11, Vol.18 (11-12), p.583-589

2016

Volltextzugriff (PDF)

JS07.5.A PROGNOSTIC FACTORS ASSOCIATED WITH POOR OUTCOME IN ADULT PATIENTS WITH MEDULLOBLASTOMA

Neuro-oncology (Charlottesville, Va.), 2023-09, Vol.25 (Supplement_2), p.ii11-ii11

2023

Volltextzugriff (PDF)

Medulloblastomas: review

Revue neurologique, 2011-05, Vol.167 (5), p.431-448

2011

Volltextzugriff (PDF)

Chromosomes en puzzle, le chromothripsis

Revue d'Oncologie Hématologie Pédiatrique, 2013-06, Vol.1 (1), p.41-43

Bourdeaut, F.

2013

Volltextzugriff (PDF)

Germline Mutations of the Paired–Like Homeobox 2B ( PHOX2B) Gene in Neuroblastoma

American journal of human genetics, 2004-04, Vol.74 (4), p.761-764

2004

Volltextzugriff (PDF)

Hyperexpression, mutation, amplification… de quoi parle-t-on ?

Revue d'Oncologie Hématologie Pédiatrique, 2014-06, Vol.2 (2), p.99-104

2014

Volltextzugriff (PDF)

Tumeur et développement (TED) : un enregistrement national des associations de cancers pédiatriques et de pathologies malformatives

Revue d'Oncologie Hématologie Pédiatrique, 2014-06, Vol.2 (2), p.70-77

2014

Volltextzugriff (PDF)

L’alliance parents-enfant-soignants à l’épreuve de l’erreur médicale

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-12, Vol.17 (12), p.1696-1708

2010

Volltextzugriff (PDF)

NSRG-05. SAFETY OF ULTRASOUND-INDUCED BLOOD-BRAIN BARRIER OPENING IN PEDIATRIC PATIENTS WITH REFRACTORY SUS-TENTORIAL MALIGNANT BRAIN TUMORS BEFORE CHEMOTHERAPY ADMINISTRATION – THE SONOKID CLINICAL TRIAL

Neuro-oncology (Charlottesville, Va.), 2018-06, Vol.20 (suppl_2), p.i146-i146

2018

Volltextzugriff (PDF)

Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

Journal of medical genetics, 2010-12, Vol.47 (12), p.859-862

2010

Volltextzugriff (PDF)

L’erreur serait de cacher

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2015-08, Vol.22 (8), p.899-899

2015

Volltextzugriff (PDF)

Clinical, Radiological, Histopathological, Molecular Description and Identification of Prognostic Factors for Desmoplastic Infantile Gangliogliomas and Astrocytomas: A Multicentric Cohort Study

Pediatric blood & cancer, 2019, Vol.66 (4, SI), p.S176-S177

2019

Volltextzugriff (PDF)

Prognostic classification of pediatric medulloblastoma based on chromosome 17p loss, expression of MYCC and MYCN, and Wnt pathway activation

Neuro-oncology (Charlottesville, Va.), 2012-02, Vol.14 (2), p.203-214

2012

Volltextzugriff (PDF)

1 – 25 von 73

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(65)
Mit Volltextzugriff
(62)

Publikationsform

Artikel
(73)

Sprache

Englisch
(47)
Französisch
(26)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)

Imaging Features with Histopathologic Correlation of CNS High-Grade Neuroepithelial Tumors with a BCOR Internal Tandem Duplication

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort

Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRI

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group

Malformations, genetic abnormalities, and wilms tumor

Indications and results of diagnostic biopsy in pediatric renal tumors: A retrospective analysis of 317 patients with critical review of SIOP guidelines

Silence would be the greatest error

Rhabdoid component emerging as a subclonal evolution of paediatric glioneuronal tumours

In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin

Rhadboid tumours: hSNF/INI1 deficient cancers of early childhood with aggressive behaviour

Les émotions dans la relation de soin : des racines de leur répression aux enjeux de leur expression

Prédispositions génétiques en oncologie pédiatrique

JS07.5.A PROGNOSTIC FACTORS ASSOCIATED WITH POOR OUTCOME IN ADULT PATIENTS WITH MEDULLOBLASTOMA

Medulloblastomas: review

Chromosomes en puzzle, le chromothripsis

Germline Mutations of the Paired–Like Homeobox 2B ( PHOX2B) Gene in Neuroblastoma

Hyperexpression, mutation, amplification… de quoi parle-t-on ?

Tumeur et développement (TED) : un enregistrement national des associations de cancers pédiatriques et de pathologies malformatives

L’alliance parents-enfant-soignants à l’épreuve de l’erreur médicale

NSRG-05. SAFETY OF ULTRASOUND-INDUCED BLOOD-BRAIN BARRIER OPENING IN PEDIATRIC PATIENTS WITH REFRACTORY SUS-TENTORIAL MALIGNANT BRAIN TUMORS BEFORE CHEMOTHERAPY ADMINISTRATION – THE SONOKID CLINICAL TRIAL

Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

L’erreur serait de cacher

Clinical, Radiological, Histopathological, Molecular Description and Identification of Prognostic Factors for Desmoplastic Infantile Gangliogliomas and Astrocytomas: A Multicentric Cohort Study

Prognostic classification of pediatric medulloblastoma based on chromosome 17p loss, expression of MYCC and MYCN, and Wnt pathway activation

Suchergebnisse filtern