Frederic Brioude

Frederic Brioude

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Frederic Brioude

Frederic Brioude

Publications by authors named "Frederic Brioude"

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44Publications

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Overgrowth syndromes - clinical and molecular aspects and tumour risk.

Nat Rev Endocrinol 2019 05;15(5):299-311

Sorbonne Université, INSERM UMR_S938, Centre de Recherche Saint Antoine, AP-HP Hôpital Trousseau, Paris, France.

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http://www.nature.com/articles/s41574-019-0180-z
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http://dx.doi.org/10.1038/s41574-019-0180-zDOI Listing
May 2019

CUGC for Simpson-Golabi-Behmel syndrome (SGBS).

Eur J Hum Genet 2019 Apr 25;27(4):663-668. Epub 2019 Jan 25.

Service de Génétique, Centre Hospitalier Universitaire, Tours, France.

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http://www.nature.com/articles/s41431-019-0339-z
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http://dx.doi.org/10.1038/s41431-019-0339-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460641PMC
April 2019

Roles of Type 1 Insulin-Like Growth Factor (IGF) Receptor and IGF-II in Growth Regulation: Evidence From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion.

Front Endocrinol (Lausanne) 2019 30;10:263. Epub 2019 Apr 30.

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, Paris, France.

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https://www.frontiersin.org/article/10.3389/fendo.2019.00263
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http://dx.doi.org/10.3389/fendo.2019.00263DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503735PMC
April 2019

Corpus Callosum Abnormalities and Short Femurs in Beckwith-Wiedemann Syndrome: A Report of Two Fetal Cases.

Fetal Pediatr Pathol 2018 Dec 31;37(6):411-417. Epub 2018 Dec 31.

a Unité d'Embryofœtopathologie, Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP , Paris , France.

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http://dx.doi.org/10.1080/15513815.2018.1520942DOI Listing
December 2018

Placental Pathology in Beckwith-Wiedemann Syndrome According to Genotype/Epigenotype Subgroups.

Fetal Pediatr Pathol 2018 Dec 11;37(6):387-399. Epub 2019 Jan 11.

a Department of Pathology , Centre hospitalier Lyon Sud , Hospices Civils de Lyon, Pierre Bénite, Lyon , France.

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http://dx.doi.org/10.1080/15513815.2018.1504842DOI Listing
December 2018

Diagnosis and management of postnatal fetal growth restriction.

Best Pract Res Clin Endocrinol Metab 2018 08 5;32(4):523-534. Epub 2018 Apr 5.

Sorbonne Université, INSERM, UMR_S 938 Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, F-75012, Paris, France. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S1521690X183006
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http://dx.doi.org/10.1016/j.beem.2018.03.013DOI Listing
August 2018

Comment on: Juvenile granulosa cell ovarian tumor in a child with Beckwith-Wiedemann syndrome.

Pediatr Blood Cancer 2017 08 11;64(8). Epub 2017 Jan 11.

AP-HP, Hôpitaux Universitaires Paris Est (AP-HP) Hôpital des Enfants Armand Trousseau, Service d'Explorations Fonctionnelles Endocriniennes, 75012, Paris, France.

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http://dx.doi.org/10.1002/pbc.26452DOI Listing
August 2017

Imprinted disorders and growth.

Ann Endocrinol (Paris) 2017 Jun 4;78(2):112-113. Epub 2017 May 4.

AP-HP, hôpital Armand-Trousseau, explorations fonctionnelles endocriniennes, Inserm, UMR_S 938, centre de recherche Saint-Antoine, Sorbonne Universities, UPMC université Paris 06, 26, avenue du Docteur-Arnold-Netter, 75012 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.ando.2017.04.010DOI Listing
June 2017

Study of the Factors Leading to Fetal and Neonatal Dysthyroidism in Children of Patients With Graves Disease.

J Endocr Soc 2017 Jun 25;1(6):751-761. Epub 2017 Apr 25.

Department of Neonatology, Obstetrics and Gynecology, University Hospitals Paris Nord Val de Seine, Assistance Publique Hôpitaux de Paris, Beaujon Hospital, Clichy 92118, France.

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http://dx.doi.org/10.1210/js.2017-00189DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677510PMC
June 2017

Hypercortisolism due to a Pituitary Adenoma Associated with Beckwith-Wiedemann Syndrome.

Horm Res Paediatr 2016 3;86(3):206-211. Epub 2016 Jun 3.

UPMC Univ Paris 06, Sorbonne Universités, Paris, France.

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http://dx.doi.org/10.1159/000446435DOI Listing
April 2017

Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy?

Pediatr Blood Cancer 2016 09 27;63(9):1571-7. Epub 2016 May 27.

Sorbonne Universités, UPMC Univ Paris 06, APHP Hôpital Armand Trousseau Pediatric Surgery, Centre de Recherche St Antoine, Inserm UMRS.938, 75012 Paris, France.

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http://dx.doi.org/10.1002/pbc.26073DOI Listing
September 2016

New clinical and molecular insights into Silver-Russell syndrome.

Curr Opin Pediatr 2016 08;28(4):529-35

aAP-HP, Hôpital Armand Trousseau, Explorations Fonctionnelles EndocriniennesbCentre de Recherche Saint Antoine, INSERM UMR_S938cSorbonne Universities, UPMC UNIV PARIS 06, Paris, France.

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http://dx.doi.org/10.1097/MOP.0000000000000379DOI Listing
August 2016

Human imprinting anomalies in fetal and childhood growth disorders: clinical implications and molecular mechanisms.

Curr Pharm Des 2014 ;20(11):1751-63

Explorations Fonctionnelles Endocriniennes, Hopital Armand Trousseau, Pierre & Marie Curie School of Medicine, INSERM UMR-S938, 26 Av du Dr Arnold Netter, 75012, France.

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http://dx.doi.org/10.2174/13816128113199990525DOI Listing
December 2014

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.

Hum Mol Genet 2014 Nov 10;23(21):5763-73. Epub 2014 Jun 10.

INSERM, UMR_S 938, CDR Saint-Antoine, Paris F-75012, France, Sorbonne Universités, UPMC Univ Paris 06, UMR_S 938, CDR Saint-Antoine, Paris F-75012, France, Pediatric Endocrinology, APHP, Armand Trousseau Hospital, Paris, France,

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http://dx.doi.org/10.1093/hmg/ddu290DOI Listing
November 2014

CDKN1C mutations: two sides of the same coin.

Trends Mol Med 2014 Nov 25;20(11):614-22. Epub 2014 Sep 25.

Institute of Human Genetics, University Hospital, Technical University Aachen, Aachen, Germany.

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http://dx.doi.org/10.1016/j.molmed.2014.09.001DOI Listing
November 2014

Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation.

Hum Mutat 2014 Oct 22;35(10):1211-20. Epub 2014 Aug 22.

INSERM, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France; Sorbonne Universités, UPMC Univ Paris 06, UMR_S 938, CDR Saint-Antoine, Paris, F-75012, France; APHP, Armand Trousseau Hospital, Pediatric Endocrinology, Paris, France.

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http://dx.doi.org/10.1002/humu.22623DOI Listing
October 2014

SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.

Eur J Med Genet 2013 Oct 24;56(10):546-50. Epub 2013 Jul 24.

APHP, Groupe hospitalier Pitié-Salpêtrière, Département de Génétique et Cytogénétique, Paris, France; Université Pierre et Marie Curie, Faculté de Médecine, Paris, France; INSERM UMRS 975, CNRS UMR 725, Paris, France.

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http://dx.doi.org/10.1016/j.ejmg.2013.06.005DOI Listing
October 2013

Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes.

Endocr Dev 2012 23;23:60-70. Epub 2012 Nov 23.

Laboratoire d'Explorations Fonctionnelles Endocriniennes, APHP, Hôpital Armand Trousseau, INSERM UMRS-938 team 4, Université Pierre et Marie Curie-Paris 6, Paris, France.

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http://dx.doi.org/10.1159/000341750DOI Listing
May 2013

[Is there a relationship between the growth hormone dose and tumoral or cardiovascular complications?].

Bull Acad Natl Med 2012 Jan;196(1):127-35; discussion 135-7

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January 2012

Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.

Eur J Endocrinol 2010 May 5;162(5):835-51. Epub 2010 Mar 5.

Université Paris-Sud 11 and INSERM U 693, Faculté de Médecine Paris Sud, Le Kremlin Bicêtre, France.

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http://dx.doi.org/10.1530/EJE-10-0083DOI Listing
May 2010

[Epigenetics, genomic imprinting and developmental disorders].

Bull Acad Natl Med 2010 Feb;194(2):287-97; discussion 297-300

UPMC ParisVI-INSERM UMRS.938, Paris, France.

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February 2010