Franck Bourdeaut

Franck Bourdeaut

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Franck Bourdeaut

Publications by authors named "Franck Bourdeaut"

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SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation.

Acta Neuropathol 2019 Apr 8;137(4):675-678. Epub 2019 Mar 8.

Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.

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http://dx.doi.org/10.1007/s00401-019-01983-4DOI Listing
April 2019

[Constitutional MMR deficiency: Genetic bases and clinical implications].

Bull Cancer 2019 Feb 11;106(2):162-172. Epub 2018 Dec 11.

Paris Sciences Lettres Research University, institut Curie, département de génétique, 75005 Paris, France; Sorbonne Universités, UPMC université Paris 06, Centre de recherche Saint-Antoine, Inserm, CNRS, 75012 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.bulcan.2018.10.008DOI Listing
February 2019

Genetic predisposition to medulloblastomas: just follow the tumour genome.

Lancet Oncol 2018 06 9;19(6):722-723. Epub 2018 May 9.

SIREDO Pediatric Cancer Center, INSERM U830, Institut Curie, Paris 75005, France.

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http://dx.doi.org/10.1016/S1470-2045(18)30289-4DOI Listing
June 2018

Enrollment in early-phase clinical trials in pediatric oncology: The experience at Institut Curie.

Pediatr Blood Cancer 2018 05 15;65(5):e26916. Epub 2018 Jan 15.

Department of Pediatric Oncology, Oncology Center SIREDO (Care, Innovation, Research for Children, Adolescents and Young Adults with Cancer), Institut Curie, Paris, France.

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http://dx.doi.org/10.1002/pbc.26916DOI Listing
May 2018

NRL and CRX Define Photoreceptor Identity and Reveal Subgroup-Specific Dependencies in Medulloblastoma.

Cancer Cell 2018 03;33(3):435-449.e6

Institut Curie - Recherche, Laboratoire 110, Centre Universitaire, Orsay Cedex 91405, France; INSERM U1021, Centre Universitaire, Orsay 91405, France; CNRS UMR 3347, Centre Universitaire, Orsay 91405, France; Université Paris Sud-11, 91405 Orsay, France; PSL Research University, Paris, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S15356108183005
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http://dx.doi.org/10.1016/j.ccell.2018.02.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368680PMC
March 2018

Ultrasound Presentation of a Disseminated Fetal and Neonatal Rhabdoid Tumor.

Case Rep Obstet Gynecol 2018 31;2018:6073204. Epub 2018 Jan 31.

Department of Obstetrics and Gynaecology, CHU de Rennes, Hospital Anne de Bretagne, 16 Bd de Bulgarie, BP 90347, 35 203 Rennes Cedex 2, France.

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https://www.hindawi.com/journals/criog/2018/6073204/
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http://dx.doi.org/10.1155/2018/6073204DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833875PMC
January 2018

Same-day genomic and epigenomic diagnosis of brain tumors using real-time nanopore sequencing.

Acta Neuropathol 2017 11 21;134(5):691-703. Epub 2017 Jun 21.

Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), Paris, France.

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http://dx.doi.org/10.1007/s00401-017-1743-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645447PMC
November 2017

High-Throughput Drug Screening Identifies Pazopanib and Clofilium Tosylate as Promising Treatments for Malignant Rhabdoid Tumors.

Cell Rep 2017 Nov;21(7):1737-1745

Paris-Sciences-Lettres Research University, Institut Curie Research Center, SiRIC, Laboratory of Translational Research in Pediatric Oncology, Paris 75005, France; Paris-Sciences-Lettres Research University, Institut Curie Research Center, INSERM U830, Laboratory of Biology and Genetics of Cancers, Paris 75005, France; Paris-Sciences-Lettres Research University, Institut Curie Hospital, Department of Pediatric Oncology- Adolescents and Young Adults, Paris 75005, France. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2017.10.076DOI Listing
November 2017

Renal Medullary Carcinoma: Establishing Standards in Practice.

J Oncol Pract 2017 07;13(7):414-421

Vanderbilt University Medical Center, Nashville; St Jude Children's Research Hospital, Memphis, TN; University of Texas MD Anderson Cancer Center; Baylor College of Medicine, Houston, TX; American University of Beirut Medical Center, Beirut, Lebanon; Université Paris-Est Créteil, Créteil; Institut Curie; University Pierre and Marie Curie, Paris, France; University of North Carolina at Chapel Hill, Chapel Hill, NC; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston; Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA; Johns Hopkins University, Baltimore, MD; Memorial Sloan Kettering Cancer Center, New York, NY; and University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1200/JOP.2017.020909DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508447PMC
July 2017

Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.

Clin Cancer Res 2017 Jun;23(12):e62-e67

Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts.

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http://dx.doi.org/10.1158/1078-0432.CCR-17-0595DOI Listing
June 2017

Right to know and right to ignore in paediatric oncogenetics: Identifying biological causes, or seeking for meaning?

Authors:
Franck Bourdeaut

Eur J Cancer 2016 08 9;63:53-4. Epub 2016 Jun 9.

Paris Sciences-Lettres Research University, Institut Curie, Departement d'Oncologie Pediatrique-Adolescents et Jeunes adultes, 26 rue d'Ulm, 75005 Paris, France; SiRIC Institut Curie, Laboratoire de Recherche Translationnelle en Oncologie Pediatrique, Institut Curie, 26 rue d'Ulm, 75005 Paris, France; INSERM U830, Genetique et Biologie des Cancers, Institut Curie, 26 rue d'Ulm, 75005 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.ejca.2016.04.021DOI Listing
August 2016

Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas.

Eur Urol 2016 06 1;69(6):1055-61. Epub 2015 Oct 1.

INSERM U830, Génétique et Biologie des Cancers, Institut Curie, Paris, France; SiRIC Institut Curie, Recherche Translationnelle en Oncologie Pediatrique, Paris, France; Institut Curie, Département d'Oncologie Pédiatrique -Adolescents Jeunes Adultes, Paris, France.

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http://dx.doi.org/10.1016/j.eururo.2015.09.027DOI Listing
June 2016

Atypical teratoid/rhabdoid tumors-current concepts, advances in biology, and potential future therapies.

Neuro Oncol 2016 06 10;18(6):764-78. Epub 2016 Jan 10.

Children's Hospital and Swabian Children's Cancer Center, Augsburg, Germany (M.C.F.); Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California (J.A.B.); INSERM U830, Laboratory of Genetics and Biology of Cancers, and Department of Pediatric Oncology, Curie Institute, Paris, France (F.B.); Comprehensive Cancer Center and Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee (C.W.M.R.); Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts (S.N.C.); Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts (S.N.C.); Department of Pediatrics, Harvard Medical School, Boston, Massachusetts (S.N.C.).

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http://dx.doi.org/10.1093/neuonc/nov264DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864253PMC
June 2016

SMARCA4-Mutated Atypical Teratoid/Rhabdoid Tumor with Retained BRG1 Expression.

Pediatr Blood Cancer 2016 Mar 15;63(3):568-9. Epub 2015 Oct 15.

Inserm U830, Unité de Génétique et Biologie des Cancers, Institut Curie, Paris, France.

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http://dx.doi.org/10.1002/pbc.25772DOI Listing
March 2016

Congenital Disseminated Extrarenal Malignant Rhabdoid Tumor.

Pediatr Dev Pathol 2015 Sep-Oct;18(5):401-4. Epub 2015 Mar 9.

1 Service d'Anatomie et de Cytologie Pathologiques, Hôpital d'Enfants Armand Trousseau, 26 Avenue du Dr Arnold Netter, 75571 Paris Cedex 12, France, and Université Pierre et Marie Curie, Paris 6, France.

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http://dx.doi.org/10.2350/14-07-1533-CR.1DOI Listing
February 2016

Embryonal tumors with multilayered rosettes in children: the SFCE experience.

Childs Nerv Syst 2016 Feb 5;32(2):299-305. Epub 2015 Oct 5.

Department of Pediatric Hematology-Oncology, APHM, La Timone Hospital, 264 rue Saint-Pierre, 13005, Marseille, France.

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http://dx.doi.org/10.1007/s00381-015-2920-2DOI Listing
February 2016

SWI/SNF chromatin remodeling and human malignancies.

Annu Rev Pathol 2015 27;10:145-71. Epub 2014 Oct 27.

Unité de Génétique Somatique.

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http://dx.doi.org/10.1146/annurev-pathol-012414-040445DOI Listing
June 2015

Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis.

Neurology 2015 Jan 5;84(2):141-7. Epub 2014 Dec 5.

From the Manchester Centre for Genomic Medicine (M.J.S., W.G.N., D.G.E.) and University of Manchester Biomedical Imaging Institute (S.J.M.), Manchester Academic Health Sciences Centre, and Centre for Imaging Sciences (S.J.M.), University of Manchester, UK; Service de Dermatologie (S.B.) and Service de Genetique Medicale (B.I.), CHU Nantes, France; Institut für Klinische Chemie und Laboratoriumsdiagnostik Universitätsklinikum Jena (C.B.), Germany; Centre for Genomic Medicine (S.G.W., S.S.B., J.O., B.A., S.B.D., J.E.U., W.G.N., D.G.E.), St. Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, UK; INSERM U830 (W.R., F.B.), Laboratoire de Genetique et Biologie des Cancers, Paris, France; Department of Clinical Genetics (A.F.), Alder Hey Children's Hospital, Liverpool, UK; Department of Medical Genetics (C.F.R.), Oslo University Hospital, Norway; International Neuroscience Institute (A.S.), Hannover, Germany; Department of Cellular Pathology and Greater Manchester Neurosciences Centre (D.d.P.), Salford Royal Hospitals NHS Foundation Trust; Department of Clinical Genetics (D.H.), Oxford Radcliffe Hospitals NHS Trust, UK; and Institut Curie (F.B.), SIRIC and Departement d'Oncologie Pediatrique d'Adolescents et Jeunes Adultes, Paris, France.

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http://www.neurology.org/content/84/2/141.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000112
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http://dx.doi.org/10.1212/WNL.0000000000001129DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336087PMC
January 2015

[Biology of cancer and leukemia in childhood].

Rev Prat 2014 Nov;64(9):1270-2

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November 2014

Non-rhabdoid pediatric SMARCB1-deficient tumors: overlap between chordomas and malignant rhabdoid tumors?

Cancer Genet 2014 Sep 23;207(9):384-9. Epub 2014 May 23.

Department of Biopathology, Centre Léon Bérard, Lyon, France.

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http://dx.doi.org/10.1016/j.cancergen.2014.05.005DOI Listing
September 2014

Rhabdoid tumors: integrating biological insights with clinical success: a report from the SMARCB1 and Rhabdoid Tumor Symposium, Paris, December 12-14, 2013.

Cancer Genet 2014 Sep 24;207(9):346-51. Epub 2014 Oct 24.

Swabian Children's Cancer Center, Children's Hospital Augsburg and EU-RHAB Center, Augsburg, Germany.

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http://dx.doi.org/10.1016/j.cancergen.2014.10.004DOI Listing
September 2014

Cutaneous location of atypical teratoid/rhabdoid tumour.

Acta Derm Venereol 2014 Jul;94(4):454-6

Department of Dermatology, Descartes-Paris V University, Necker-Enfants Malades Hospital, Paris, France.

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http://www.medicaljournals.se/acta/content/?doi=10.2340/0001
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http://dx.doi.org/10.2340/00015555-1716DOI Listing
July 2014

SegAnnDB: interactive Web-based genomic segmentation.

Bioinformatics 2014 Jun 3;30(11):1539-46. Epub 2014 Feb 3.

Department of Computer Science, Tokyo Institute of Technology, Tokyo 152-8552, Japan, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, INSERM U900, Paris F-75248, France, Mines ParisTech, Centre for Computational Biology, 77300 Fontainebleau, Unité de Recherche en Génomique Végétale INRA-CNRS-Université d'Evry Val d'Essonne, Évry 91057, France, INSERM U830, Paris F-75248, France, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya-city 464-8681, Japan and INRIA-Sierra Project-Team, Département d'Informatique de l'École Normale Supérieure, Paris F-75013, FranceDepartment of Computer Science, Tokyo Institute of Technology, Tokyo 152-8552, Japan, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, INSERM U900, Paris F-75248, France, Mines ParisTech, Centre for Computational Biology, 77300 Fontainebleau, Unité de Recherche en Génomique Végétale INRA-CNRS-Université d'Evry Val d'Essonne, Évry 91057, France, INSERM U830, Paris F-75248, France, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya-city 464-8681, Japan and INRIA-Sierra Project-Team, Département d'Informatique de l'École Normale Supérieure, Paris F-75013, FranceDepartment of Computer Science, Tokyo Institute of Technology, Tokyo 152-8552, Japan, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, INSERM U900, Paris F-75248, France, Mines ParisTech, Centre for Computational Biology, 77300 Fontainebleau, Unité de Recherche en Génomique Végétale INRA-CNRS-Université d'Evry Val d'Essonne, Évry 91057, France, INSERM U830, Paris F-75248, France, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya-city 464-8681, Japan and INRIA-Sierra Project-Team, Département d'Informatique de l'École Normale Supérieure, Paris F-75013, France.

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http://dx.doi.org/10.1093/bioinformatics/btu072DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029035PMC
June 2014

Cytogenetic prognostication within medulloblastoma subgroups.

J Clin Oncol 2014 Mar 3;32(9):886-96. Epub 2014 Feb 3.

David J.H. Shih, Marc Remke, Vijay Ramaswamy, Betty Luu, Yuan Yao, Xin Wang, Adrian M. Dubuc, Livia Garzia, John Peacock, Stephen C. Mack, Xiaochong Wu, Adi Rolider, A. Sorana Morrissy, Florence M.G. Cavalli, Claudia C. Faria, Stephen W. Scherer, Uri Tabori, Cynthia E. Hawkins, David Malkin, Eric Bouffet, James T. Rutka, and Michael D. Taylor, Hospital for Sick Children; David J.H. Shih, Marc Remke, Vijay Ramaswamy, Yuan Yao, Xin Wang, Adrian M. Dubuc, John Peacock, Stephen C. Mack, and Michael D. Taylor, University of Toronto, Toronto; Boleslaw Lach, McMaster University, Hamilton, Ontario; Jennifer A. Chan, University of Calgary, Calgary, Alberta; Steffen Albrecht, Adam Fontebasso, and Nada Jabado, McGill University, Montreal, Quebec, Canada; Paul A. Northcott, Andrey Korshunov, Marcel Kool, David T.W. Jones, and Stefan M. Pfister, German Cancer Research Center; Stefan M. Pfister, University Hospital Heidelberg, Heidelberg; Ulrich Schüller, Ludwig-Maximilians-University, Munich; Stefan Rutkowski, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Karel Zitterbart, Masaryk University School of Medicine; Karel Zitterbart and Leos Kren, University Hospital Brno, Brno, Czech Republic; Toshihiro Kumabe and Teiji Tominaga, Tohoku University Graduate School of Medicine, Sendai, Japan; Young Shin Ra, University of Ulsan, Asan Medical Center; Ji-Yeoun Lee, Byung-Kyu Cho, Seung-Ki Kim, and Kyu-Chang Wang, Seoul National University Children's Hospital, Seoul; Shin Jung, Chonnam National University Research Institute of Medical Sciences, Chonnam National University Hwasun Hospital and Medical School, Chonnam, South Korea; Peter Hauser and Miklós Garami, Semmelweis University, Budapest; László Bognár and Almos Klekner, University of Debrecen, Medical and Health Science Centre, Debrecen, Hungary; Shenandoah Robinson, Boston Children's Hospital; Scott L. Pomeroy, Harvard Medical School, Boston, MA; Ali G. Saad, University of Arkansas for Medical Sciences, Little

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http://dx.doi.org/10.1200/JCO.2013.50.9539DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948094PMC
March 2014

Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition.

Cancer Cell 2014 Mar;25(3):393-405

Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), 69121 Heidelberg, Germany; Department of Pediatric Oncology, Hematology and Immunology, University Hospital Heidelberg, 69120 Heidelberg, Germany.

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http://dx.doi.org/10.1016/j.ccr.2014.02.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493053PMC
March 2014

Rubinstein-Taybi syndrome predisposing to non-WNT, non-SHH, group 3 medulloblastoma.

Pediatr Blood Cancer 2014 Feb 20;61(2):383-6. Epub 2013 Sep 20.

INSERMU830, Laboratoire de génétique et biologie des cancers, Institut Curie, Paris, France; Département de pédiatrie, Institut Curie, Paris, France.

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http://dx.doi.org/10.1002/pbc.24765DOI Listing
February 2014

TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma.

Acta Neuropathol 2013 Dec 31;126(6):917-29. Epub 2013 Oct 31.

The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.

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http://dx.doi.org/10.1007/s00401-013-1198-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830749PMC
December 2013

Extracranial rhabdoid tumours: what we have learned so far and future directions.

Lancet Oncol 2013 Jul;14(8):e329-36

Department of Paediatric Oncology, Royal Manchester Children's Hospital, Manchester, UK.

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http://dx.doi.org/10.1016/S1470-2045(13)70088-3DOI Listing
July 2013

[Genetic predisposition to bone tumors].

Authors:
Franck Bourdeaut

Soins Pediatr Pueric 2013 Jan-Feb(270):19

Département de pédiatrie, Inserm U830, Laboratoire de génétique et biologie des cancers, Institut Curie, 75005 Paris, France.

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March 2013

Germline mutations in FGF receptors and medulloblastomas.

Am J Med Genet A 2013 Feb 16;161A(2):382-5. Epub 2013 Jan 16.

INSERMU830, Laboratoire de génétique et biologie des cancers, Institut Curie, Paris, France.

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http://dx.doi.org/10.1002/ajmg.a.35719DOI Listing
February 2013

[Chromatin remodeling defects and cancer: the SWI/SNF example].

Bull Cancer 2012 Dec;99(12):1133-40

Institut Curie, département d'oncologie pédiatrique, Inserm U830-laboratoire de génétique et biologie des cancers, 26, rue d'Ulm, 75248 Paris Cedex 05, France.

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http://dx.doi.org/10.1684/bdc.2012.1664DOI Listing
December 2012

[Subtypes of medulloblastomas: distinct cellular origins].

Med Sci (Paris) 2012 Oct 12;28(10):805-9. Epub 2012 Oct 12.

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http://dx.doi.org/10.1051/medsci/20122810003DOI Listing
October 2012

[Medulloblastoma in childhood: an heterogeneous disease requiring treatment adjustments to known risk factors].

Rev Prat 2012 Sep;62(7):989-90

Département d'oncologie pédiatrique, Institut Curie, Paris, France.

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September 2012

Medulloblastomas: update on a heterogeneous disease.

Curr Opin Oncol 2011 Nov;23(6):630-7

Département de Pédiatrie, Institut Curie, Paris, France.

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https://insights.ovid.com/crossref?an=00001622-201111000-000
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http://dx.doi.org/10.1097/CCO.0b013e32834ace3fDOI Listing
November 2011

Shall we treat hydrocephalus associated to brain stem glioma in children?

Childs Nerv Syst 2011 Oct 17;27(10):1735-9. Epub 2011 Sep 17.

Department of Paediatric Neurosurgery, Hôpital Necker Enfants Malades, APHP, 149, rue de sèvres, 75015 Paris, France.

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http://dx.doi.org/10.1007/s00381-011-1538-2DOI Listing
October 2011

Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.

Am J Med Genet A 2011 Jul 10;155A(7):1763-6. Epub 2011 Jun 10.

CHU Nantes, service d'hemato-oncologie pédiatrique, France.

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http://dx.doi.org/10.1002/ajmg.a.34066DOI Listing
July 2011

Extra-renal non-cerebral rhabdoid tumours.

Pediatr Blood Cancer 2008 Sep;51(3):363-8

Institut Curie, Departement de Pediatrie, Paris, France.

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http://dx.doi.org/10.1002/pbc.21632DOI Listing
September 2008

Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders.

Pediatr Blood Cancer 2008 Apr;50(4):908-11

Institut Curie, Département de Pédiatrie, Paris F-75246, France.

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http://dx.doi.org/10.1002/pbc.21255DOI Listing
April 2008

Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.

Eur J Cancer 2007 Nov 31;43(16):2366-72. Epub 2007 Aug 31.

Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM U-781, et Département de Génétique, Université René-Descartes, Faculté de Médecine, Hôpitaux de Paris, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France.

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http://dx.doi.org/10.1016/j.ejca.2007.07.016DOI Listing
November 2007

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.

Cancer Lett 2005 Oct;228(1-2):51-8

Laboratoire de Pathologie Moléculaire des Cancers, INSERM U-509, Institut Curie, 26 rue d'Ulm, 75248 Paris Cedex 05, France.

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http://dx.doi.org/10.1016/j.canlet.2005.01.055DOI Listing
October 2005

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.

Am J Hum Genet 2004 Apr 11;74(4):761-4. Epub 2004 Mar 11.

Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U-393, and Département de Génétique, Hôpital Necker-Enfants Malades, Paris, France.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970761902
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http://dx.doi.org/10.1086/383253DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1181953PMC
April 2004

Propionibacterium acnes chest infections in patients with chronic granulomatous disease: case reports.

Clin Infect Dis 2002 Mar 31;34(6):853-4. Epub 2002 Jan 31.

Unité d'Immunologie et Hématologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, France.

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http://academic.oup.com/cid/article/34/6/853/387162
Publisher Site
http://dx.doi.org/10.1086/338875DOI Listing
March 2002