Publications by authors named "Catherine Dodé"

55Publications

Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome.

Ann Endocrinol (Paris) 2017 Oct 12;78(5):455-461. Epub 2017 Aug 12.

Département universitaire d'anatomie de Rockefeller, UFR médecine Lyon-Est, 8, avenue Rockefeller, 69373 Lyon, France; Service de radiologie, centre hospitalier Lyon-Sud, hospices civils de Lyon, 165, chemin du Grand-Revoyet, 69495 Pierre-Bénite, France; CREATIS, CNRS UMR 5220 Inserm U1044, université Lyon 1, 7, avenue Jean-Capelle, 69621 Villeurbanne, France. Electronic address:

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http://dx.doi.org/10.1016/j.ando.2016.12.003DOI Listing
October 2017

Digenic MEFV/TNFRSF1A autoinflammatory syndrome with relapsing aseptic neutrophilic meningitis and chronic myelitis.

Clin Exp Rheumatol 2017 Nov-Dec;35 Suppl 108(6):128-129. Epub 2017 Jan 26.

Université Paris-Diderot, Assistance Publique Hôpitaux de Paris, Département de Médecine Interne, Hôpital Bichat-Claude Bernard, Paris, France.

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February 2018

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.

J Clin Endocrinol Metab 2016 12 7;101(12):4541-4550. Epub 2016 Sep 7.

Inserm 1185 (J.B., I.B., S.B., J.F., J.Y., N.B.), Le Kremlin-Bicêtre, Université Paris-Saclay, Faculté de Médecine Paris Sud, 94270 Le Kremlin-Bicêtre, France; Service de Biochimie et Génétique Moléculaire (K.A., C.B., C.D.), Hôpital Cochin, AP-HP, Université Paris-Descartes, 75004 Paris, France; Service d'Endocrinologie-Diabète-Nutrition (A.F., B.D.), CHU de Reims-Hôpital Robert-Debré, 51100 Reims, France; Institut Jacques Monod (A.L.T., R.A.V.), Université Paris Diderot-PARIS 7/CNRS UMR7592, 75013 Paris, France; and Service d'Endocrinologie et des Maladies de la Reproduction (J.Y.), APHP, Hôpital de Bicêtre, 94270 Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1210/jc.2016-2152DOI Listing
December 2016

Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency.

J Clin Endocrinol Metab 2015 Oct 24;100(10):E1378-85. Epub 2015 Jul 24.

Harvard Reproductive Endocrine Sciences Center and Reproductive Endocrine Unit (J.-H.C., R.B., N.D.S., J.E.H., L.P., C.L.B., W.F.C.), and Department of Medicine, Psychiatric, and Neurodevelopmental Genetics Unit (P.H.L.), Analytic and Translational Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, and Center for Human Genetic Research (J.F.G.), Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, Massachusetts Boston, Massachusetts 02114; Department of Genetics (M.-L.K.), University Hospital, Caen, 14003, Caen Cedex, France; Department of Biology and Pathology of Human Reproduction in Bialystok (K.J.), Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, and Department of Reproduction and Gynecological Endocrinology (S.W.), Medical University of Bialystok, Sklodowskiej 24A, 15-276 Bialystok, Poland; Institute for Genetic Medicine (R.Q.), Newcastle University, Newcastle-upon-Tyne, NE1 3BZ, United Kingdom; Disciplina de Endocrinologia (A.C.L.), Hospital das Clinicas da Faculdade de Medicina, Universidade de Sao Paulo, 05403-900 Sao Paulo, Brazil; Laboratoire de Biochimie et Génétique Moléculaire (C.D.), Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Université Paris-Descartes, 75014 Paris, France; Departments of Molecular Endocrinology and Pediatrics (T.O.), Hamamatsu University of School of Medicine, Hamamatsu 431-3192, Japan; Section of Reproductive Endocrinology, Infertility, and Genetics (H.-G.K., L.C.L.), Departments of Obstetrics and Gynecology and Neuroscience and Regenerative Medicine, Medical College of Georgia at Georgia Regents University, Augusta, Georgia 30912; and Department of Pediatrics (J.-H.C.), Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul 138-736, Republic of Korea.

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http://dx.doi.org/10.1210/jc.2015-2262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596034PMC
October 2015

New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.

J Clin Endocrinol Metab 2015 Mar 16;100(3):994-1001. Epub 2014 Dec 16.

Inserm U693 (J.B., J.B., A.G.M., J.Y., N.B.), Le Kremlin-Bicêtre, F-94276, France; Université Paris-Sud (J.B., J.Y., N.B.), Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre, F-94276, France; Service d'Hormonologie, d'Endocrinologie Moléculaire et Des Maladies Rares (F.R.-B.), Centre De Biologie et Pathologie Est, Université Lyon 1, 69677 Bron, France; Unité de Gynécologie Endocrinienne (A.G.), Université Paris-Descartes, l'Assistance Publique-Hôpitaux de Paris, Hôpitaux Universitaires Paris Centre, 75014 Paris, France; l'Assistance Publique-Hôpitaux de Paris (H.B-G., J.Y., N.B.), Hôpital de Bicêtre, Service d'Endocrinologie et des Maladies de la Reproduction, Le Kremlin-Bicêtre, F-94276, France; Centre d'Aide Médicale à la Procréation (H.B-G.), CHI 94000 Créteil, France; Service de Biochimie et Génétique Moléculaire (K.A., C.B., C.D.), Hôpital Cochin, l'Assistance Publique-Hôpitaux de Paris Université Paris-Descartes, 75006 Paris, France; l'Assistance Publique-Hôpitaux de Paris (J.B., A.G.M.), Service de Génétique Moléculaire, Pharmacogénétique et Hormonologie, Le Kremlin-Bicêtre, F-94276, France; and Service d'Endocrinologie-Diabète-Nutrition (A.-C.H., B.D.), Centre Hospitalier Universitaire de Reims-Hôpital Robert-Debré, 51092 Reims, France.

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http://dx.doi.org/10.1210/jc.2014-2761DOI Listing
March 2015

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

J Clin Endocrinol Metab 2014 Oct 31;99(10):E2138-43. Epub 2014 Jul 31.

EA7331 Faculté des Sciences Pharmaceutiques (S.M., C.D.), 75006 Paris, France; Laboratoire de Biologie et Génétique Moléculaires (J.S., C.L., C.F., C.D.), Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, 75014 Paris, France; Service de Pédiatrie et de Génétique Médicale (P.P., C.M.), Centre Hospitalier Universitaire Morvan, 29200 Brest, France; Department of Reproduction and Gynecological Endocrinology (S.W.), PL-15-1276 Bialystok, Poland; Service de Génétique (M.G.), Centre Hospitalier Régional Clémenceau, 14033 Caen, France; Service de Génétique Médicale (E.B.), Hôpital Purpan, 31059 Toulouse, France; Service de Pédiatrie (F.K.), Hôpital Bel Air, 57126 Thionville, France; Service d'Edocrinologie (O.V.-M.), Centre Hospitalier, 59322 Valenciennes, France; UF de Génétique Clinique (L.P.), Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, 75019 Paris, France; Service de Médecine et d'Endocrinologie (F.A.), Hôpital du Cluzeau, 87042 Limoges, France; Service d'Endocrinologie (S.C.), Hôpital Trousseau, and Service d'Endocrinologie (S.C.-M.), Hôpital St Antoine, Assistance Publique-Hôpitaux de Paris, 75012 Paris, France; Service d'Endocrinologie (P.R.), Centre Hospitalier, 49933 Angers, France; Department of Clinical Genetics (H.H.), University Hospital, DK-1165 Copenhagen, Denmark; Department of Medical Genetics (T.P.), Hospital HF Rikshospital, 0424 Oslo, Norway; Service de Génétique Médicale (D.L.), Hôpital Pellegrin, 33076 Bordeaux, France; Service d'Endocrinologie (P.T.), Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, 75013 Paris, France; Service d'Endocrinologie (S.H.), Hôpital l'Archet, 06003 Nice, France; Service de Gynécologie Endocrinienne (D.D.), Hôpital Jeanne de Flandre, 59037 Lille, France; Service d'Endocrinologie (J.Y.), Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris, 94275 Le Kremlin-Bicêtre, France; and Service d'Endocrinologie (M.P.), Hôpital Neurologiqu

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http://dx.doi.org/10.1210/jc.2014-2110DOI Listing
October 2014

Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations.

FASEB J 2014 Aug 15;28(8):3734-44. Epub 2014 May 15.

Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) 5203, Institut de Génomique Fonctionnelle, Montpellier, France; Institut National de la Santé et de la Recherche Médicale (INSERM) U661, Montpellier, France; Université Montpellier 1 and 2, Montpellier, France;

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http://dx.doi.org/10.1096/fj.13-243402DOI Listing
August 2014

Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.

Eur J Endocrinol 2013 Dec 21;169(6):805-9. Epub 2013 Oct 21.

Département de Génétique et Développement, Institut Cochin, Inserm U1016, Université Paris-Descartes, Paris, France.

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http://dx.doi.org/10.1530/EJE-13-0419DOI Listing
December 2013

PROK2/PROKR2 Signaling and Kallmann Syndrome.

Front Endocrinol (Lausanne) 2013 12;4:19. Epub 2013 Apr 12.

INSERM U1016, Institut Cochin, Université Paris-Descartes Paris, France.

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http://dx.doi.org/10.3389/fendo.2013.00019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624607PMC
April 2013

Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism.

Nat Rev Endocrinol 2011 Oct 18;8(3):172-82. Epub 2011 Oct 18.

Departement de Pédiatrie Endocrinienne, Hôpital Bicêtre-University Paris-Sud, 78 Rue du Général Leclerc, F-94275 Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1038/nrendo.2011.164DOI Listing
October 2011

[Kallmann syndrome - a fetopathological sequence].

Med Sci (Paris) 2011 Feb 8;27(2):135-7. Epub 2011 Mar 8.

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http://dx.doi.org/10.1051/medsci/2011272135DOI Listing
February 2011

Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions.

J Clin Invest 2010 Oct;120(10):3668-72

INSERM U1016, Département de Génétique et Développement, Institut Cochin, Université Paris-Descartes, Paris, France.

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http://www.jci.org/articles/view/43699
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http://dx.doi.org/10.1172/JCI43699DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2947242PMC
October 2010

Kallmann syndrome.

Eur J Hum Genet 2009 Feb 5;17(2):139-46. Epub 2008 Nov 5.

Inserm U567, Département de Génétique et Développement, Institut Cochin, Paris, France.

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http://dx.doi.org/10.1038/ejhg.2008.206DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2986064PMC
February 2009

PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.

Hum Mol Genet 2009 Jan 29;18(1):75-81. Epub 2008 Sep 29.

CNRS UMR5203, Institut de Génomique Fonctionnelle, INSERM U661, Université Montpellier 1,2, Montpellier, France.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddn318DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298864PMC
January 2009

Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome.

Eur J Hum Genet 2008 Jul 20;16(7):865-8. Epub 2008 Feb 20.

Laboratoire de biochimie et génétique moléculaire, hôpital Cochin, APHP, Paris, France.

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http://www.nature.com/articles/ejhg200815
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http://dx.doi.org/10.1038/ejhg.2008.15DOI Listing
July 2008

Dramatic etanercept-induced remission of relapsing febrile sciatic neuralgia related to p46l mutation of the tnfrsf1a gene.

Clin Rheumatol 2007 Sep 29;26(9):1535-6. Epub 2006 Aug 29.

Service de Médecine Interne, du Professeur Pierre Jean Weiller, CHU de La Timone, 264 rue Saint Pierre, 13385 Marseille Cedex 05, France.

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http://dx.doi.org/10.1007/s10067-006-0418-8DOI Listing
September 2007

Intestinal pseudo-obstruction as a manifestation of tumor necrosis factor receptor-associated periodic syndrome.

Dig Dis Sci 2006 Jun;51(6):1061-2

Department of Internal Medicine, Centre Hospitalier Universitaire de Rouen-Boisguillaume, Rouen Cedex, France.

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http://link.springer.com/10.1007/s10620-006-8009-8
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http://dx.doi.org/10.1007/s10620-006-8009-8DOI Listing
June 2006

Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean fever.

C R Biol 2006 Feb 10;329(2):71-4. Epub 2006 Jan 10.

Laboratoire de génétique, Institut national d'hygiène, 11400 Rabat, Morocco.

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http://dx.doi.org/10.1016/j.crvi.2005.11.005DOI Listing
February 2006

Coexistence of Kallmann syndrome and complete androgen insensitivity in the same patient.

Eur J Endocrinol 2005 Jun;152(6):813-7

Service d'Endocrinologie, Service d'Orthopédie, Hôtel-Dieu de France Hospital, Beirut, Lebanon.

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http://dx.doi.org/10.1530/eje.1.01915DOI Listing
June 2005

Amyloidosis and auto-inflammatory syndromes.

Curr Drug Targets Inflamm Allergy 2005 Feb;4(1):57-65

Service de médecine interne, L'Hôtel-Dieu, Assistance publique-hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.2174/1568010053622786DOI Listing
February 2005

[Hereditary intermittant fever].

Presse Med 2004 Oct;33(17):1195-206

Service de médecine interne, Hôtel-Dieu, Assistance publique-Hôpitaux de Paris.

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http://dx.doi.org/10.1016/s0755-4982(04)98889-6DOI Listing
October 2004

Kallmann syndrome: fibroblast growth factor signaling insufficiency?

J Mol Med (Berl) 2004 Nov 8;82(11):725-34. Epub 2004 Sep 8.

Institut Cochin et Laboratoire de Biochimie et Génétique Moléculaire, Hôpital Cochin, 24 rue du Faubourg Saint-Jacques, 75014, Paris, France.

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http://dx.doi.org/10.1007/s00109-004-0571-yDOI Listing
November 2004

[Kallmann De Morsier syndrome: FGF-signaling insufficiency?].

Med Sci (Paris) 2004 Aug-Sep;20(8-9):793-8

Institut Cochin et Laboratoire de Biochimie et génétique moléculaire, Hôpital Cochin, 24, rue du Faubourg Saint-Jacques, 75014 Paris, France.

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http://dx.doi.org/10.1051/medsci/2004208-9793DOI Listing
April 2005

TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis.

J Nephrol 2003 May-Jun;16(3):435-7

Department of Biochemical Genetics, Cochin Hospital, Paris.

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July 2003

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Brain 2003 Jul 6;126(Pt 7):1599-603. Epub 2003 May 6.

INSERM U289, Hôpital de la Salpêtrière, 47 Bd de l'Hôpital, 75013 Paris, France.

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http://dx.doi.org/10.1093/brain/awg155DOI Listing
July 2003

Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks.

Nephrol Dial Transplant 2002 Jul;17(7):1212-7

Laboratoire de biochimie et génétique moléculaire, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

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http://dx.doi.org/10.1093/ndt/17.7.1212DOI Listing
July 2002

[Hereditary intermittent fevers, other than familial Mediterranean fevers].

Rev Prat 2002 Jan;52(2):155-9

Service de médecine interne L'Hôtel-Dieu 75181 Paris.

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January 2002