Publications by authors named "Bettina Bessières"

52Publications

Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renalhepatic-pancreatic dysplasia.

Kidney Int 2020 Oct 28. Epub 2020 Oct 28.

Laboratoire des Maladies rénales héréditaires, Institut Imagine, Inserm U1163, Université de Paris, France; APHP, Néphrologie pédiatrique, Centre de Référence MARHEA, Hôpital universitaire Necker-Enfants malades, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.kint.2020.09.029DOI Listing
October 2020

Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease.

Cell Rep 2020 Oct;33(4):108304

Université de Paris, Institut Necker-Enfants Malades (INEM), Epigenetics and Development Team, INSERM U1151, CNRS UMR 8253, 75015 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2020.108304DOI Listing
October 2020

Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?

Clin Genet 2020 Sep 14. Epub 2020 Sep 14.

Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, Assistance Publique - Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1111/cge.13840DOI Listing
September 2020

Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy.

Am J Obstet Gynecol 2020 08 10;223(2):256.e1-256.e9. Epub 2020 Apr 10.

Department of Obstetrics and Maternal-Fetal Medicine, Necker-Enfants Malades Hospital, AP-HP and Paris Descartes University; EHU FETUS, Université de Paris and IMAGINE Institute. Electronic address:

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http://dx.doi.org/10.1016/j.ajog.2020.02.052DOI Listing
August 2020

Congenitally corrected transposition of the great arteries: is it really a transposition? An anatomical study of the right ventricular septal surface.

J Anat 2020 02 27;236(2):325-333. Epub 2019 Oct 27.

Laboratory of Anatomy of Congenital Heart Disease - M3C, Hôpital Marie Lannelongue, Le Plessis-Robinson, France.

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http://dx.doi.org/10.1111/joa.13097DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956431PMC
February 2020

Fetal MRI findings in a retrospective cohort of 26 cases of prenatally diagnosed CHARGE syndrome individuals.

Prenat Diagn 2019 08 3;39(9):781-791. Epub 2019 Apr 3.

Service de Radiologie, Hôpital Necker Enfants Malades, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.

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http://dx.doi.org/10.1002/pd.5429DOI Listing
August 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

Two-Port Fetoscopic Repair of Myelomeningocele in Fetal Lambs.

Fetal Diagn Ther 2019 21;45(1):36-41. Epub 2018 Feb 21.

Department of Fetal Medicine, Armand Trousseau Hospital, APHP, Sorbonne University, UPMC Paris 6 University, Paris,

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http://dx.doi.org/10.1159/000485655DOI Listing
April 2019

Stress-induced unfolded protein response contributes to Zika virus-associated microcephaly.

Nat Neurosci 2018 01 11;21(1):63-71. Epub 2017 Dec 11.

GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège, C.H.U. Sart Tilman, Liège, Belgium.

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http://dx.doi.org/10.1038/s41593-017-0038-4DOI Listing
January 2018

Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations.

Birth Defects Res 2017 Nov 31;109(19):1586-1595. Epub 2017 Jul 31.

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

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http://dx.doi.org/10.1002/bdr2.1093DOI Listing
November 2017

Fetoscopic patch coverage of experimental myelomenigocele using a two-port access in fetal sheep.

Childs Nerv Syst 2017 Jul 26;33(7):1177-1184. Epub 2017 May 26.

Service de Médecine Foetale, Hôpital Armand Trousseau, APHP, 26 avenue du Docteur Arnold Netter, 75012, Paris, France.

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http://dx.doi.org/10.1007/s00381-017-3461-7DOI Listing
July 2017

Discordances Between Pre-Natal and Post-Natal Diagnoses of Congenital Heart Diseases and Impact on Care Strategies.

J Am Coll Cardiol 2016 08;68(9):921-30

Unité Médico-Chirurgicale de Cardiologie Congénitale et Pédiatrique, Centre de Référence Malformations Cardiaques Congénitales Complexes, M3C, Hôpital Necker Enfants Malades, Assistance publique hôpitaux de Paris, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

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http://dx.doi.org/10.1016/j.jacc.2016.05.087DOI Listing
August 2016

First fetal case of the 8q24.3 contiguous genes syndrome.

Am J Med Genet A 2016 Jan 5;170A(1):239-42. Epub 2015 Oct 5.

Department of Histology-Embryology and Cytogenetics, Necker-Enfants Malades Hospital, AP-HP, Paris, France.

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http://dx.doi.org/10.1002/ajmg.a.37411DOI Listing
January 2016

Pulmonary hypoplasia associated with congenital heart diseases: a fetal study.

PLoS One 2014 3;9(4):e93557. Epub 2014 Apr 3.

AP-HP, Hôpital Necker-Enfants Malades, Service de Pneumologie Pédiatrique, Centre de Référence pour les Maladies Respiratoires Rares de l'Enfant, Paris, France; INSERM UMR 781, Paris, France; Université Paris-Descartes, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0093557PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974773PMC
February 2015

Early neonatal death and congenital left coronary abnormalities: ostial atresia, stenosis and anomalous aortic origin.

Arch Cardiovasc Dis 2013 Apr 9;106(4):202-8. Epub 2013 Mar 9.

Centre de référence malformations cardiaques congénitales complexes-M3C-Necker, hôpital Necker enfants-malades, assistance publique des hôpitaux de Paris, université Paris Descartes, Sorbonne Paris-Cité, Paris, France.

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http://dx.doi.org/10.1016/j.acvd.2013.01.002DOI Listing
April 2013

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

Am J Med Genet A 2012 Nov 17;158A(11):2797-806. Epub 2012 Sep 17.

Craniofacial Development and Stem Cell Biology, Comprehensive Biomedical Research Centre, Dental Institute, King's College London, Guy's Hospital, London, United Kingdom.

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http://doi.wiley.com/10.1002/ajmg.a.35598
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http://dx.doi.org/10.1002/ajmg.a.35598DOI Listing
November 2012

Disseminated congenital toxoplasma infection with a type II strain.

Pediatr Infect Dis J 2011 Sep;30(9):813-5

Neonatal Intensive Care Unit, Institut de Puériculture, Paris, France.

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http://dx.doi.org/10.1097/INF.0b013e31821b8dfeDOI Listing
September 2011

[Pathology of the placenta. Case 8. Sickle cell trait].

Ann Pathol 2010 Aug 29;30(4):310-2. Epub 2010 Jul 29.

Laboratoire d'anatomo-fœtopathologie, institut de puériculture, 26, boulevard Brune, 75014 Paris, France.

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http://dx.doi.org/10.1016/j.annpat.2010.05.009DOI Listing
August 2010

[Pathology of the placenta. Case 2. Cytomegalovirus placentitis].

Ann Pathol 2010 Aug 29;30(4):280-4. Epub 2010 Jul 29.

Laboratoire d'anatomo fœtopathologie, institut de puériculture, 26, boulevard Brune, 75014 Paris, France.

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http://dx.doi.org/10.1016/j.annpat.2010.05.003DOI Listing
August 2010

Fowler syndrome-a clinical, radiological, and pathological study of 14 cases.

Am J Med Genet A 2010 Jan;152A(1):153-60

Department of Clinical Genetics, Birmingham Women's Hospital NHS Foundation Trust, Birmingham, UK.

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http://dx.doi.org/10.1002/ajmg.a.33094DOI Listing
January 2010

Re-evaluation of the role of STOX1 transcription factor in placental development and preeclampsia.

J Reprod Immunol 2009 Nov 3;82(2):174-81. Epub 2009 Jul 3.

Equipe 21, Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France.

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http://dx.doi.org/10.1016/j.jri.2009.05.001DOI Listing
November 2009