Maithe Tauber

Maithe Tauber

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Maithe Tauber

Publications by authors named "Maithe Tauber"

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Equivocal expression of emotions in children with Prader-Willi syndrome: what are the consequences for emotional abilities and social adjustment?

Orphanet J Rare Dis 2020 Feb 21;15(1):55. Epub 2020 Feb 21.

Centre de Référence du Syndrome de Prader-Willi, CHU Toulouse, Toulouse, France.

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http://dx.doi.org/10.1186/s13023-020-1333-9DOI Listing
February 2020

A study of voice and non-voice processing in Prader-Willi syndrome.

Orphanet J Rare Dis 2020 Jan 20;15(1):22. Epub 2020 Jan 20.

Prader-Willi Syndrome Reference Center, Children's Hospital-INSERM-University of Toulouse Paul Sabatier, Toulouse, France.

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http://dx.doi.org/10.1186/s13023-020-1298-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972021PMC
January 2020

Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girl.

J Pediatr Endocrinol Metab 2019 Nov;32(11):1295-1298

Paediatric Endocrine Unit, Children's Hospital, Purpan University Hospital, Toulouse, France.

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http://dx.doi.org/10.1515/jpem-2019-0082DOI Listing
November 2019

Causes of death in Prader-Willi syndrome: lessons from 11 years' experience of a national reference center.

Orphanet J Rare Dis 2019 11 4;14(1):238. Epub 2019 Nov 4.

Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, Toulouse, France.

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http://dx.doi.org/10.1186/s13023-019-1214-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829836PMC
November 2019

Letter regarding "Prevalence of growth hormone deficiency in previously GH-treated young adults with Prader-Willi syndrome" by Donze et al.

Clin Endocrinol (Oxf) 2019 Oct 26;91(4):578-579. Epub 2019 Jun 26.

President IPWSO, Department of Psychiatry, University of Cambridge, Cambridge, UK.

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http://dx.doi.org/10.1111/cen.14047DOI Listing
October 2019

Prader-Willi syndrome: A model for understanding the ghrelin system.

J Neuroendocrinol 2019 Jul 23;31(7):e12728. Epub 2019 May 23.

Unité d'Endocrinologie Pédiatrique, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1111/jne.12728DOI Listing
July 2019

Growth Hormone Treatment for Prader-Willi Syndrome.

Pediatr Endocrinol Rev 2018 Sep;16(Suppl 1):91-99

Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU Toulouse, France, Axe Pédiatrique du CIC 9302/INSERM. Hôpital des Enfants, Toulouse, France, INSERM U1043, Centre de Physiopathologie de Toulouse Purpan, UPS, France.

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https://www.pediatricendoreviews.com/
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http://dx.doi.org/10.17458/per.vol16.2018.tdm.ghpraderwilliDOI Listing
September 2018

[Childhood obesity].

Rev Prat 2018 Jun;68(6):e233-e240

Hôpital des Enfants, 31059 Toulouse Cedex 9, France.

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June 2018

[Obesities do not all require the same care].

Rev Prat 2018 Jun;68(6):e241

Hôpital des Enfants, 31059 Toulouse Cedex 9, France.

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June 2018

A model to characterize psychopathological features in adults with Prader-Willi syndrome.

Am J Med Genet A 2018 01 17;176(1):41-47. Epub 2017 Nov 17.

Euskal Herriko Unibertsitatea-University of the Basque Country, Psychobiology, Donostia, Spain.

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http://dx.doi.org/10.1002/ajmg.a.38525DOI Listing
January 2018

Final height and intrauterine growth retardation.

Authors:
Maïthé Tauber

Ann Endocrinol (Paris) 2017 Jun 4;78(2):96-97. Epub 2017 May 4.

Unité d'endocrinologie, obésité, maladies osseuses, génétique et gynécologie médicale, hôpital des Enfants, CHU de Toulouse, 330, avenue de Grande-Bretagne, TSA 70034, 31059 Toulouse cedex 9, France; Institut national de la santé et de la recherche médicale unité 1043, centre de physiopathologie de Toulouse Purpan, université Paul-Sabatier, Toulouse, France. Electronic address:

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http://dx.doi.org/10.1016/j.ando.2017.04.005DOI Listing
June 2017

Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome.

Orphanet J Rare Dis 2017 06 28;12(1):118. Epub 2017 Jun 28.

Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, 330, avenue de Grande-Bretagne, TSA 40031 - 31059, Toulouse cedex 9, France.

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http://dx.doi.org/10.1186/s13023-017-0673-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490212PMC
June 2017

Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome.

J Clin Endocrinol Metab 2016 12 23;101(12):4895-4903. Epub 2016 Sep 23.

Assistance Publique-Hôpitaux de Paris (M.C., J.-M.O., K.C., C.P.), Pitié-Salpêtrière Hospital, Nutrition Department, French Reference Centre for Prader-Willi Syndrome, and Institute of Cardiometabolism and Nutrition (J.-M.O., K.C., C.P.), Sorbonne University, Université Pierre et Marie Curie, Unité Mixte de Recherche 1166, Nutriomic Team Pitié-Salpêtrière Hospital, Paris F-75013, France; Department of Endocrinology, Bone Diseases, Genetics, and Gynaecology (M.T.), Children's Hospital, French Reference Centre for Prader-Willi Syndrome, Toulouse F-31059 France and Université Paul Sabatier, Toulouse III F-31062, France; Inserm (M.T.), 1043 Team 12, Human Physiopathology Centre, and Department of Medical Genetics (E.B.), Purpan Hospital, Toulouse F-31059, France; Assistance Publique-Hôpitaux de Paris (L.C.), Laboratory of Biochemistry and Molecular Genetics, Institut Cochin and Cochin Hospital, Université Paris Descartes, Paris F-75014, France; Assistance Publique-Hôpitaux de Paris (V.L.), French Reference Center for Prader-Willi Syndrome, Hôpital Marin d'Hendaye, Hendaye F-64701, France; and Assistance Publique-Hôpitaux de Paris (J.-M.L.), Pitié-Salpêtrière Hospital, Department of Endocrine and Oncology Biochemistry, Paris F-75013 France.

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http://dx.doi.org/10.1210/jc.2016-2163DOI Listing
December 2016

Sequelae of GH Treatment in Children with PWS.

Pediatr Endocrinol Rev 2016 Dec;14(2):138-146

Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU Toulouse, France, Axe Pédiatrique du CIC 9302/INSERM. Hôpital des Enfants, Toulouse, France, Centre de Physiopathologie de Toulouse-Purpan, Université de Toulouse, CNRS UMR 5282, INSERM UMR 1043, Université Paul Sabatier, Toulouse, France.

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http://dx.doi.org/10.17458/PER.2016.TDM.SequelaeofGHDOI Listing
December 2016

Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.

Stem Cell Res 2016 11 16;17(3):526-530. Epub 2016 Aug 16.

Columbia University, Department of Pediatrics, Division of Molecular Genetics, United States; Naomi Berrie Diabetes Center, United States; New York Obesity Research Center, United States. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2016.08.008DOI Listing
November 2016

Dyssynchrony and perinatal psychopathology impact of child disease on parents-child interactions, the paradigm of Prader Willi syndrom.

J Physiol Paris 2016 11 1;110(4 Pt B):427-433. Epub 2017 Sep 1.

Unité d'Endocrinologie, Obésité, Maladies Osseuses, Génétique et Gynécologie Médicale, Centre de Référence du Syndrome de Prader-Willi, Hôpital des Enfants, Toulouse, France; Axe Pédiatrique du CIC 9302/INSERM, Hôpital des Enfants, Toulouse, France; INSERM U1043, Centre de Physiopathologie de Toulouse Purpan, UPS, France.

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http://dx.doi.org/10.1016/j.jphysparis.2017.08.001DOI Listing
November 2016

Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits.

Hum Mol Genet 2016 08 10;25(15):3208-3215. Epub 2016 Jun 10.

The Saban Research Institute, Developmental Neuroscience Program, Children's Hospital Los Angeles, University of Southern California, Department of Pediatrics, Los Angeles, CA 90027, USA

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http://dx.doi.org/10.1093/hmg/ddw169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179922PMC
August 2016

Gonadotropin-Releasing Hormone Agonist Treatment in Sexual Precocity.

Endocr Dev 2016 17;29:214-29. Epub 2015 Dec 17.

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http://dx.doi.org/10.1159/000438893DOI Listing
July 2016

Growth patterns of patients with Noonan syndrome: correlation with age and genotype.

Eur J Endocrinol 2016 May 22;174(5):641-50. Epub 2016 Feb 22.

EndocrineBone Diseases, and Genetics Unit, Children's Hospital, Toulouse University Hospital, Toulouse, France INSERM UMR 1043Centre of Pathophysiology of Toulouse Purpan (CPTP), University of Toulouse Paul Sabatier, Toulouse, France

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http://dx.doi.org/10.1530/EJE-15-0922DOI Listing
May 2016

Deficits in voice and multisensory processing in patients with Prader-Willi syndrome.

Neuropsychologia 2016 05 16;85:137-47. Epub 2016 Mar 16.

Université Toulouse, CerCo, Université Paul Sabatier, Toulouse, France; CNRS, UMR 5549, Faculté de Médecine de Purpan, Toulouse, France. Electronic address:

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http://dx.doi.org/10.1016/j.neuropsychologia.2016.03.015DOI Listing
May 2016

High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome.

Orphanet J Rare Dis 2016 05 4;11(1):56. Epub 2016 May 4.

Unité d'Endocrinologie, Obésité, Maladies Osseuses, Génétique et Gynécologie Médicale. Centre de Référence du Syndrome de Prader-Willi, Hôpital des Enfants, Toulouse, France.

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http://dx.doi.org/10.1186/s13023-016-0440-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855494PMC
May 2016

[Children with mental disabilities are at high risk for obesity].

Rev Prat 2016 02;66(2):133-136

Hôpital des enfants, CHU Toulouse, Toulouse, France.

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February 2016

Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi Syndrome: a matched control study.

Surg Obes Relat Dis 2016 Jan 26;12(1):213-4. Epub 2015 Sep 26.

Institute of Cardiometabolism and Nutrition (ICAN), and French Reference Centre of Prader-Willi Syndrome, Department of Endocrinology, Bone Diseases, Genetics, and Gynaecology, Children's Hospital, Toulouse, France; French Reference Centre of Prader-Willi Syndrome, Department of Endocrinology, Bone Diseases, Genetics, and Gynaecology, Children's Hospital, Toulouse, France.

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http://dx.doi.org/10.1016/j.soard.2015.09.015DOI Listing
January 2016

[Obesity and overweight of children and adolescents].

Authors:
Maïthé Tauber

Rev Prat 2015 Dec;65(10):1263

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December 2015

[Hypothalamus and behavior: the model Prader-Willi syndrome].

Authors:
Maïthé Tauber

Rev Prat 2015 Dec;65(10):1273-4

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December 2015

[Organization of care for obese children and teenagers].

Authors:
Maïthé Tauber

Rev Prat 2015 Dec;65(10):1283-4

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December 2015

[Prader-Willi syndrome in 2015].

Med Sci (Paris) 2015 Oct 19;31(10):853-60. Epub 2015 Oct 19.

Génétique médicale, hôpital Purpan, CHU de Toulouse, France.

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http://dx.doi.org/10.1051/medsci/20153110011DOI Listing
October 2015

Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype.

J Bone Miner Res 2015 Aug 14;30(8):1369-76. Epub 2015 May 14.

Endocrine, Bone Diseases, and Genetics Unit, Children's Hospital, Toulouse University Hospital, Toulouse, France.

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http://dx.doi.org/10.1002/jbmr.2471DOI Listing
August 2015

Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders.

Front Neuroanat 2014 20;8:164. Epub 2015 Jan 20.

Institut de Neurobiologie de la Méditerranée Unité Mixe de Recherche U901, Institut National de la Santé et de la Recherche Médicale, Parc Scientifique de Luminy Marseille, France ; Aix-Marseille Université, Institut de Neurobiologie de la Méditerranée Unité Mixe de Recherche 901 Marseille, France.

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http://dx.doi.org/10.3389/fnana.2014.00164DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4341354PMC
March 2015

Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.

Eur J Hum Genet 2015 Feb 11;23(2):252-5. Epub 2014 Jun 11.

1] Centre de Physiopathologie de Toulouse-Purpan, INSERM UMR 1043; CNRS UMR 5282, Université Paul Sabatier, Toulouse, France [2] Centre de Référence du Syndrome de Prader-Willi, Toulouse, France [3] Unité d'Endocrinologie, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.

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http://dx.doi.org/10.1038/ejhg.2014.103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297892PMC
February 2015

Prader-Willi syndrome as a model of human hyperphagia.

Front Horm Res 2014 7;42:93-106. Epub 2014 Apr 7.

Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.

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http://dx.doi.org/10.1159/000358317DOI Listing
December 2014

LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity.

Proc Natl Acad Sci U S A 2014 Oct 6;111(42):E4494-503. Epub 2014 Oct 6.

Institut National de la Santé et de la Recherche Médicale, U1048, F-31432 Toulouse, France; Institut des Maladies Métaboliques et Cardiovasculaires, Université de Toulouse, Université Paul Sabatier, F-31432 Toulouse, France;

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http://dx.doi.org/10.1073/pnas.1406107111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210352PMC
October 2014

Clinical utility gene card for: Prader-Willi Syndrome.

Eur J Hum Genet 2014 Sep 16;22(9). Epub 2014 Apr 16.

Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

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http://dx.doi.org/10.1038/ejhg.2014.66DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135421PMC
September 2014

Towards optimal treatment with growth hormone in short children and adolescents: evidence and theses.

Horm Res Paediatr 2013 26;79(2):51-67. Epub 2013 Feb 26.

Paediatric Endocrinology Section, Children's Hospital, University of Tuebingen, Tuebingen, Germany.

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http://dx.doi.org/10.1159/000347121DOI Listing
September 2013

Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables.

J Neurodev Disord 2013 Aug 6;5(1):18. Epub 2013 Aug 6.

Centre de Référence Prader-Willi, Hôpital Marin AP-HP, Hendaye, France.

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http://dx.doi.org/10.1186/1866-1955-5-18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751283PMC
August 2013

GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.

J Clin Endocrinol Metab 2013 Jun 29;98(6):E1072-87. Epub 2013 Mar 29.

Research Center and Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine, Montréal, Québec, Canada H3T 1C5.

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http://dx.doi.org/10.1210/jc.2012-3888DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789886PMC
June 2013

Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19.

Mol Cell Endocrinol 2012 Jan 21;348(1):313-21. Epub 2011 Sep 21.

Laboratorio de Biología Molecular, Cátedra de Genética y Biología Molecular, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, 1113 Buenos Aires, Argentina.

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https://linkinghub.elsevier.com/retrieve/pii/S03037207110055
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http://dx.doi.org/10.1016/j.mce.2011.09.024DOI Listing
January 2012

Elevated insulin-like growth factor-I values in children with Prader-Willi syndrome compared with growth hormone (GH) deficiency children over two years of GH treatment.

J Clin Endocrinol Metab 2010 Oct;95(10):4600-8

Department of Endocrinology, Bone Diseases, Genetics, and Gynaecology, Centre de Référence du Syndrome de Prader-Willi, Children's Hospital, Toulouse, France.

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http://dx.doi.org/10.1210/jc.2009-1831DOI Listing
October 2010

[Obesity in the child].

Rev Prat 2010 Mar;60(3):393-4

Unité d'endocrinologie, maladies osseuses, génétique et gynécologie médicale, CHU Toulouse, Hôpital des enfants, 31026 Toulouse Cedex 3, France.

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March 2010

[Child obesity].

Rev Prat 2009 Sep;59(7):1005-12

Unité d'endocrinologie, maladies osseuses, génétique et gynécologie médicale, CHU Toulouse, Hôpital des enfants, 31026 Toulouse Cedex 3, France.

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September 2009

Long-acting lanreotide in adolescent girls with constitutional tall stature.

Horm Res 2009 4;71(4):228-36. Epub 2009 Mar 4.

Department of Pediatric Endocrinology and Diabetology, INSERM U690 and Centre de Référence des Maladies Endocriniennes Rares de la Croissance, Robert Debré Hospital and University Paris 7 Denis Diderot, Paris, France.

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http://search.proquest.com/openview/5920596841f5354f3778196e
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http://www.karger.com/doi/10.1159/000201112
Publisher Site
http://dx.doi.org/10.1159/000201112DOI Listing
June 2009

Network of European studies of genes in growth (NESTEGG).

Horm Res 2009 Apr 29;71 Suppl 2:48-54. Epub 2009 Apr 29.

Barts and the London Queen Mary School of Medicine, London, UK.

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http://dx.doi.org/10.1159/000192436DOI Listing
April 2009

Is scoliosis an issue for giving growth hormone to children with Prader-Willi syndrome?

Arch Dis Child 2008 Dec;93(12):1004-6

Centre de Référence du syndrome de Prader-Willi, Department of Endocrinology, Genetics, Gynaecology and Bone Diseases, Hôpital des Enfants, CHU Toulouse, France.

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http://dx.doi.org/10.1136/adc.2008.141390DOI Listing
December 2008

French database of children and adolescents with Prader-Willi syndrome.

BMC Med Genet 2008 Oct 2;9:89. Epub 2008 Oct 2.

Centre de Référence du syndrome de Prader-Willi, Division of Endocrinology, Genetics, Gynaecology and Bone Diseases, Hôpital des Enfants, and University Paul Sabatier, Toulouse, France.

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http://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2350-9-89DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569911PMC
October 2008

Scoliosis in patients with Prader-Willi Syndrome.

Pediatrics 2008 Aug 7;122(2):e499-503. Epub 2008 Jul 7.

Department of Orthopaedic Surgery, Hôpital des Enfants-Malades Assistance-Publique Hôpitaux de Paris, Faculté de Médicine Paris Descartes, Paris, France.

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http://pediatrics.aappublications.org/cgi/doi/10.1542/peds.2
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http://dx.doi.org/10.1542/peds.2007-3487DOI Listing
August 2008

Hyperghrelinemia precedes obesity in Prader-Willi syndrome.

J Clin Endocrinol Metab 2008 Jul 6;93(7):2800-5. Epub 2008 May 6.

Unit of Endocrinology, Hôpital des Enfants, 330 Avenue de Grande Bretagne, Toulouse Cedex 9, France.

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http://dx.doi.org/10.1210/jc.2007-2138DOI Listing
July 2008

[Normal puberty].

Rev Prat 2008 Jun;58(12):1311-6

Unité d'endocrinologie, génétique, pathologie osseuse et gynécologie médicale, hôpital des Enfants, Université Toulouse III, 31059 Toulouse Cedex.

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June 2008

KIGS highlights: growth hormone treatment in Prader-Willi Syndrome.

Horm Res 2007 10;68 Suppl 5:48-50. Epub 2007 Dec 10.

Hôpital des Enfants, Pediatrie-Endocrinologie, Génétique et Gynécologie Medicale, Toulouse, France.

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http://dx.doi.org/10.1159/000110475DOI Listing
March 2008

Long-term evolution of endocrine disorders and effect of GH therapy in 35 patients with pituitary stalk interruption syndrome.

Horm Res 2005 15;64(6):266-73. Epub 2005 Oct 15.

Division of Endocrinology, Genetics, Gynecology and Bone Diseases, Hôpital des Enfants, Toulouse, France.

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https://www.karger.com/Article/FullText/89425
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http://dx.doi.org/10.1159/000089425DOI Listing
December 2005

Hyperghrelinemia is a common feature of Prader-Willi syndrome and pituitary stalk interruption: a pathophysiological hypothesis.

Horm Res 2004 8;62(1):49-54. Epub 2004 Jun 8.

Division of Endocrinology, Bone Diseases, Genetics and Gynecology, Children's Hospital, INSERM U563 (CPTP), IFR 30, Hôpital Purpan, Toulouse, France.

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http://dx.doi.org/10.1159/000078862DOI Listing
December 2004

Wrist anomalies in Turner syndrome compared with Leri-Weill dyschondrosteosis: a new feature in Turner syndrome.

Eur J Pediatr 2004 Aug 9;163(8):475-81. Epub 2004 Jun 9.

Unité d'Endocrinologie, Hôpital des Enfants, 330 Avenue de Grande-Bretagne, Toulouse, France.

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http://dx.doi.org/10.1007/s00431-004-1471-4DOI Listing
August 2004

Stimulating effect of growth hormone on cytokine release in children.

Eur J Endocrinol 2003 Nov;149(5):397-401

Dipartimento di Scienze Pediatriche, Universita degli Studi di Pavia, IRCCS San Matteo, Piazzale le Golgi 2, 27100 Pavia, Italia.

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http://dx.doi.org/10.1530/eje.0.1490397DOI Listing
November 2003

NESTEGG: aims and strategies. Northern European Study of Genes in Growth.

J Pediatr Endocrinol Metab 2002 Dec;15 Suppl 5:1441-2

Paediatric Endocrinology Section, St. Bartholomew 's Hospital and the London Medical and Dental School, Queen Mary University of London, UK.

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December 2002