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Paola Cambiaso

Showing results (1-10 of 13) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 28, 2006
Non-conventional use of growth hormone therapyMarco Cappa, Graziamaria Ubertini, Diego Colabianchi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2016
Long-term first line medical treatment in a 4-year-old girl with Xq26.3 microduplication-negative somatotropinoma. Case report and literature reviewChiara Maggioli, Paola Cambiaso, Sara Ciccone, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
A CDKL5 mutated child with precocious pubertyVeronica Saletti, Laura Canafoglia, Paola Cambiaso, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Growth and pubertal growth spurt in dysmorphic syndromesMarco Cappa, Carla Bizzarri, Diego Colabianchi, et al.
Hormone Research in Paediatrics|May 1, 2019
Anti-Hypothalamus and Anti-Pituitary Auto-antibodies in ROHHAD Syndrome: Additional Evidence Supporting an Autoimmune EtiopathogenesisClaudio Giacomozzi, Federica Guaraldi, Paola Cambiaso, et al.
Clinical Endocrinology|December 11, 2012
Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoringPaola Cambiaso, Riccardo Schiaffini, Giuseppe Pontrelli, et al.
Italian Journal of Pediatrics|August 4, 2016
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experienceCarla Bizzarri, Nicole Olivini, Stefania Pedicelli, et al.
Pediatrics|November 11, 2015
Pituicytoma and Cushing's Disease in a 7-Year-Old Girl: A Mere Coincidence?Paola Cambiaso, Donato Amodio, Emidio Procaccini, et al.
Hormone Research|January 21, 2006
Autosomal-dominant isolated growth hormone deficiency (IGHD type II) with normal GH-1 geneDanilo Fintini, Roberto Salvatori, Souzan Salemi, et al.
The Journal of Pediatrics|December 26, 2006
Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndromePaola Cambiaso, Cinzia Orazi, Maria Cristina Digilio, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 28, 2006
Non-conventional use of growth hormone therapyMarco Cappa, Graziamaria Ubertini, Diego Colabianchi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2016
Long-term first line medical treatment in a 4-year-old girl with Xq26.3 microduplication-negative somatotropinoma. Case report and literature reviewChiara Maggioli, Paola Cambiaso, Sara Ciccone, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
A CDKL5 mutated child with precocious pubertyVeronica Saletti, Laura Canafoglia, Paola Cambiaso, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Growth and pubertal growth spurt in dysmorphic syndromesMarco Cappa, Carla Bizzarri, Diego Colabianchi, et al.
Hormone Research in Paediatrics|May 1, 2019
Anti-Hypothalamus and Anti-Pituitary Auto-antibodies in ROHHAD Syndrome: Additional Evidence Supporting an Autoimmune EtiopathogenesisClaudio Giacomozzi, Federica Guaraldi, Paola Cambiaso, et al.
Clinical Endocrinology|December 11, 2012
Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoringPaola Cambiaso, Riccardo Schiaffini, Giuseppe Pontrelli, et al.
Italian Journal of Pediatrics|August 4, 2016
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experienceCarla Bizzarri, Nicole Olivini, Stefania Pedicelli, et al.
Pediatrics|November 11, 2015
Pituicytoma and Cushing's Disease in a 7-Year-Old Girl: A Mere Coincidence?Paola Cambiaso, Donato Amodio, Emidio Procaccini, et al.
Hormone Research|January 21, 2006
Autosomal-dominant isolated growth hormone deficiency (IGHD type II) with normal GH-1 geneDanilo Fintini, Roberto Salvatori, Souzan Salemi, et al.
The Journal of Pediatrics|December 26, 2006
Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndromePaola Cambiaso, Cinzia Orazi, Maria Cristina Digilio, et al.
Pageof 2