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Archives of Disease in Childhood
|
March 5, 2022
Noonan syndrome: improving recognition and diagnosis
Martin Zenker, Thomas Edouard, Joanne C Blair, et al.
Italian Journal of Pediatrics
|
October 25, 2020
Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report
Stefania Pedicelli, Luca de Palma, Caterina Pelosini, et al.
Endocrine Development
|
December 18, 2010
Adrenoleukodystrophy
Marco Cappa, Carla Bizzarri, Catello Vollono, et al.
Clinical Laboratory
|
July 20, 2013
Peculiar genotypes of the autoimmune regulator gene in Italian patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
Alessia Palma, Antonino Crinó, Melania Palombi, et al.
Italian Journal of Pediatrics
|
June 27, 2013
Triple A (Allgrove) syndrome: an unusual association with syringomyelia
Carla Bizzarri, Danila Benevento, Cesare Terzi, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
June 28, 2006
Non-conventional use of growth hormone therapy
Marco Cappa, Graziamaria Ubertini, Diego Colabianchi, et al.
Diabetes/Metabolism Research and Reviews
|
December 25, 2004
An observational study comparing continuous subcutaneous insulin infusion (CSII) and insulin glargine in children with type 1 diabetes
Riccardo Schiaffini, Paolo Ciampalini, Sabrina Spera, et al.
European Journal of Pediatrics
|
September 25, 2007
An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE)
Carla Lintas, Marco Cappa, Donatella Comparcola, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 20, 2014
Routine screening by brain magnetic resonance imaging is not indicated in every girl with onset of puberty between the ages of 6 and 8 years
Stefania Pedicelli, Paola Alessio, Giuseppe Scirè, 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 review
Chiara Maggioli, Paola Cambiaso, Sara Ciccone, et al.
Page
of 21
Search research articles
Search
Showing results (21-30 of 207) with videos related to
Sort By:
Page
of 21
Archives of Disease in Childhood
|
March 5, 2022
Noonan syndrome: improving recognition and diagnosis
Martin Zenker, Thomas Edouard, Joanne C Blair, et al.
Italian Journal of Pediatrics
|
October 25, 2020
Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report
Stefania Pedicelli, Luca de Palma, Caterina Pelosini, et al.
Endocrine Development
|
December 18, 2010
Adrenoleukodystrophy
Marco Cappa, Carla Bizzarri, Catello Vollono, et al.
Clinical Laboratory
|
July 20, 2013
Peculiar genotypes of the autoimmune regulator gene in Italian patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
Alessia Palma, Antonino Crinó, Melania Palombi, et al.
Italian Journal of Pediatrics
|
June 27, 2013
Triple A (Allgrove) syndrome: an unusual association with syringomyelia
Carla Bizzarri, Danila Benevento, Cesare Terzi, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
June 28, 2006
Non-conventional use of growth hormone therapy
Marco Cappa, Graziamaria Ubertini, Diego Colabianchi, et al.
Diabetes/Metabolism Research and Reviews
|
December 25, 2004
An observational study comparing continuous subcutaneous insulin infusion (CSII) and insulin glargine in children with type 1 diabetes
Riccardo Schiaffini, Paolo Ciampalini, Sabrina Spera, et al.
European Journal of Pediatrics
|
September 25, 2007
An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE)
Carla Lintas, Marco Cappa, Donatella Comparcola, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 20, 2014
Routine screening by brain magnetic resonance imaging is not indicated in every girl with onset of puberty between the ages of 6 and 8 years
Stefania Pedicelli, Paola Alessio, Giuseppe Scirè, 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 review
Chiara Maggioli, Paola Cambiaso, Sara Ciccone, et al.
Page
of 21