Sylvie Rossignol

Sylvie Rossignol

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Sylvie Rossignol

Sylvie Rossignol

Publications by authors named "Sylvie Rossignol"

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39Publications

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Immobilization of Pb from mine sediments in metakaolin-based geomaterials.

Environ Sci Pollut Res Int 2019 May 14;26(14):14473-14482. Epub 2019 Mar 14.

Université de Limoges, IRCER UMR CNRS 7315, 12 rue de l'Atlantis, 87068, Limoges, France.

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http://link.springer.com/10.1007/s11356-019-04737-7
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http://dx.doi.org/10.1007/s11356-019-04737-7DOI Listing
May 2019

Normal Growth despite Combined Pituitary Hormone Deficiency.

Horm Res Paediatr 2019 Apr 25:1-10. Epub 2019 Apr 25.

Explorations Fonctionnelles et génétique endocriniennes, Hôpital Armand-Trousseau, AP-HP, Paris, France,

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https://www.karger.com/Article/FullText/499318
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http://dx.doi.org/10.1159/000499318DOI Listing
April 2019

Analysis of Inappropriate Admissions of Residents of Medicalized Nursing Homes to Emergency Departments: A Prospective Multicenter Study in Burgundy.

J Am Med Dir Assoc 2016 07 25;17(7):671.e1-7. Epub 2016 May 25.

Department of Geriatrics and Internal Medicine, Hospital of Champmaillot, University Hospital, Dijon, France.

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http://dx.doi.org/10.1016/j.jamda.2016.04.017DOI Listing
July 2016

Prevalence and management of gastrointestinal manifestations in Silver-Russell syndrome.

Arch Dis Child 2015 Apr 18;100(4):353-8. Epub 2014 Nov 18.

Nutrition et Gastroentérologie Pédiatrique, AP-HP, Hôpital Armand-Trousseau, Paris, France Institut de Cardiométabolisme et Nutrition (ICAN), INSERM UMRS U872 (Eq7) Nutriomique, Université Pierre et Marie Curie-Paris 6, Centre de Recherche des Cordeliers, Paris, France.

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http://dx.doi.org/10.1136/archdischild-2013-305864DOI Listing
April 2015

Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.

J Med Genet 2015 Jan 13;52(1):53-60. Epub 2014 Nov 13.

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

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http://dx.doi.org/10.1136/jmedgenet-2014-102732DOI Listing
January 2015

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

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

Genetic variants within the second intron of the KCNQ1 gene affect CTCF binding and confer a risk of Beckwith-Wiedemann syndrome upon maternal transmission.

J Med Genet 2014 Aug 4;51(8):502-11. Epub 2014 Jul 4.

Epigenetics in Human Health and Disease, Baker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australia.

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http://jmg.bmj.com/lookup/doi/10.1136/jmedgenet-2014-102368
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http://dx.doi.org/10.1136/jmedgenet-2014-102368DOI Listing
August 2014

Epigenetic anomalies in childhood growth disorders.

Nestle Nutr Inst Workshop Ser 2013 22;71:65-73. Epub 2013 Jan 22.

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/10.1159/000342568DOI Listing
October 2013

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

Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes.

Hum Mutat 2011 Feb;32(2):249-58

APHP, Hôpital Armand Trousseau, Laboratoire d'Explorations Fonctionnelles Endocriniennes, INSERM UMR-S938 Team 4, Université Pierre et Marie Curie-Paris 6, Paris, France.

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http://dx.doi.org/10.1002/humu.21403DOI Listing
February 2011

Identification of solvated species present in concentrated and dilute sodium silicate solutions by combined 29Si NMR and SAXS studies.

J Colloid Interface Sci 2010 Dec 15;352(2):309-15. Epub 2010 Sep 15.

Groupe d'Etude des Matériaux Hétérogènes (GEMH E.A. 3278), CEC, Ecole Nationale Supérieure de Céramiques Industrielles, 12 rue de l'Atlantis, 87068 Limoges Cedex, France.

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http://linkinghub.elsevier.com/retrieve/pii/S002197971001043
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http://dx.doi.org/10.1016/j.jcis.2010.09.018DOI Listing
December 2010

Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases.

Epigenetics 2010 Jul 1;5(5):373-7. Epub 2010 Jul 1.

APHP, Hôpital Armand Trousseau, Laboratoire d’Explorations Fonctionnelles Endocriniennes, INSERM UMR-S938 Team 4, Université Pierre et Marie Curie-Paris 6, Paris, France.

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http://dx.doi.org/10.4161/epi.5.5.11851DOI Listing
July 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

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.

Hum Mol Genet 2009 Dec 14;18(24):4724-33. Epub 2009 Sep 14.

Laboratoire d'Explorations Fonctionnelles Endocriniennes, APHP, Hôpital Armand Trousseau, INSERM UMR-S938 Team 4, Université Pierre et Marie Curie-Paris 6, Paris, France.

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http://dx.doi.org/10.1093/hmg/ddp435DOI Listing
December 2009

Perlman syndrome: report, prenatal findings and review.

Am J Med Genet A 2008 Oct;146A(19):2532-7

Centre de Diagnostic Prénatal, Service de Réanimation Néonatale et Pédiatrique, Centre Hospitalier Régional Félix Guyon, Saint-Denis, La Réunion, France.

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http://dx.doi.org/10.1002/ajmg.a.32391DOI Listing
October 2008

Epigenetics in Silver-Russell syndrome.

Best Pract Res Clin Endocrinol Metab 2008 Jun;22(3):403-14

Explorations fonctionnelles endocriniennes, Hôpital Trousseau (APHP); INSERM U515; Université Pierre et Marie Curie-Paris6, 26 avenue du Dr Netter, 75012 Paris, France.

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http://dx.doi.org/10.1016/j.beem.2008.01.012DOI Listing
June 2008

[Placental mesenchymal dysplasia].

Ann Pathol 2008 Apr 2;28(2):85-94. Epub 2008 Jul 2.

Service d'anatomie et cytologie pathologiques, hôpital de la Croix-Rousse, 93, Grande rue de la Croix-Rousse, 69317 Lyon cedex 04, France.

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http://dx.doi.org/10.1016/j.annpat.2008.03.005DOI Listing
April 2008

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

Nat Genet 2005 Sep 7;37(9):1003-7. Epub 2005 Aug 7.

Laboratoire d'Explorations Fonctionnelles Endocriniennes, Inserm U515 et UPMC Paris 6, Hôpital Armand Trousseau, AP-HP, 26 avenue Arnold Netter, 75012 Paris, France.

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http://dx.doi.org/10.1038/ng1629DOI Listing
September 2005

Clinical and molecular overlap in overgrowth syndromes.

Am J Med Genet C Semin Med Genet 2005 Aug;137C(1):4-11

INSERM U393, Département de Génétique Médicale, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75743 [corrected] Paris, France.

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http://dx.doi.org/10.1002/ajmg.c.30060DOI Listing
August 2005