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Showing page 1 of results 1 - 10 of about 126 pages

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Knock in of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-dependent Protein Kinase A Activation: A Model of Acrodysostosis Type 1? | ESPE2016
Stunff Catherine Le; Francoise Tilotta; Jeremy Sadoine; Denmat Dominique Le; Eric Clauser; Pierre Bougneres; Catherine Chaussain
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p98.htm
Published: 2016-08-19

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Acute Adrenal Failure in a Term Newborn with Congenital Cytomegalovirus Infection: Case Description and Review of the Literature | ESPE2015
Lucia Marseglia; Tommaso Alterio; Lauretta Manti; Tommaso Aversa; Maria Rosa Calafiore; Eloisa Gitto; Malgorzata Wasniewska
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-171.htm
Published: 2015-08-26

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Is Plasma C-Type Natriuretic Peptide Level Available for Typing and Diagnosis of Skeletal Dysplasia Cases? | ESPE2018
Cetin Sirmen Kizilcan; Damla Goksen; Samim Ozen; Hudaver Alper; Esra Isık; Huseyin Onay; Sukran Darcan
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p034.htm
Published: 2018-08-28

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Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype | ESPE2018
Emily Cottrell; Sumana Chatterjee; Gudrun Moore; Miho Ishida; James Greening; Neil Wright; Artur Bossowski; Asma Deeb; Basiri Im
http://abstracts.eurospe.org/hrp/0089/hrp0089rfc10.1.htm
Published: 2018-08-28

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Erythrocytosis as First Manifestation of Adrenal Mass | ESPE2018
Mariella Valenzise; Laura Cannavo; Giuseppina Zirilli; Graziella Iaria; Mario Lima
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p019.htm
Published: 2018-08-28

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Berardinelli Seip Congenital Lipodystrophy: A Light of Hope | ESPE2015
Campo Maria Ruiz del; Isabel Saenz Moreno; Jose Julian Revorio Gonzalez; David Araujo-Vilar
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-355.htm
Published: 2015-08-26

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