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Showing page 1 of results 1 - 6 of about 6 pages

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Severe Pre- and Postnatal Growth Retardation in a Child Harboring a Novel Homozygous IGF1 Gene Mutation | ESPE2018
Keselman Ana Claudia; Scaglia Paula Alejandra; Ayelen Martin; Romina Armando; Sanguineti Nora Maria; Mariana Gutierrez; Debora B
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p143.htm
Published: 2018-08-28

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Follow-up on Bone Health in Children with Acute Lymphoblastic Leukemia (ALL) | ESPE2018
Luciana Brenzoni; Hamilton Cassinelli; Ignacio Bergada
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p053.htm
Published: 2018-08-28

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Novel LRP5 Loss-of-function Mutation Causes Osteoporosis-pseudoglioma Syndrome | ESPE2018
Debora Braslavsky; Paula Scaglia; Nora Sanguineti; Hamilton Cassinelli; Schenstrom Olivia Ruiz; Romina Armando; Claudia Arberas;
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p036.htm
Published: 2018-08-28

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Monogenic and Digenic Gene Mutations are Present in Children with Idiopathic Short Stature (ISS) | ESPE2018
Nora Maria Sanguineti; Laura Ramirez; Ana Claudia Keselman; Paula Alejandra Scaglia; Maria Gabriela Ropelato; Maria Gabriela Bal
http://abstracts.eurospe.org/hrp/0089/hrp0089fc4.1.htm
Published: 2018-08-28

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Mutations in SGPL1, the Gene Encoding Sphingosine-1-Phosphate Lyase, Cause a Novel Form of Primary Adrenal Insufficiency with Steroid Resistant Nephrotic Syndrome | ESPE2016
Rathi Prasad; Avinaash Maharaj; Eirini Meimaridou; Paul VanVeldhoven; Federica Buonocore; Eliana Barbagaleta; Ignacio Bergada; H
http://abstracts.eurospe.org/hrp/0086/hrp0086fc15.2.htm
Published: 2016-08-19

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Bone Mineral Density Evaluation in Children with Gaucher Disease | ESPE2014
Maria Silvia Larroude; Guillermo Drelichman; Hamilton Cassinelli; Lucia Richard; Alba Ruiz; Paola Reicher; Fernanda Cuello; Vict
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d3-53.htm
Published: 2014-08-28

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