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Indian Journal of Pediatrics
|
January 15, 2019
Menstrual Cycle and Headache in Teenagers
Luigi Bianchin, Mauro Bozzola, Antonio Battistella Pier, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
February 18, 2010
Update on age at menarche in Italy: toward the leveling off of the secular trend
Franco Rigon, Luigi Bianchin, Sergio Bernasconi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 23, 2006
McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and early adult age
Patrizia Matarazzo, Roberto Lala, Maria Andreo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome
Graziano Grugni, Antonino Crinò, Sara Pagani, et al.
Pediatric Research
|
March 7, 2003
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism
Luisa De Sanctis, Damiano Romagnolo, Martina Olivero, et al.
Clinical Immunology (Orlando, Fla.)
|
February 8, 2011
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
Cinzia Mazza, Fabio Buzi, Federica Ortolani, et al.
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of 3
Search research articles
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Showing results (21-30 of 26) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 26 results.
Indian Journal of Pediatrics
|
January 15, 2019
Menstrual Cycle and Headache in Teenagers
Luigi Bianchin, Mauro Bozzola, Antonio Battistella Pier, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
February 18, 2010
Update on age at menarche in Italy: toward the leveling off of the secular trend
Franco Rigon, Luigi Bianchin, Sergio Bernasconi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 23, 2006
McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and early adult age
Patrizia Matarazzo, Roberto Lala, Maria Andreo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome
Graziano Grugni, Antonino Crinò, Sara Pagani, et al.
Pediatric Research
|
March 7, 2003
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism
Luisa De Sanctis, Damiano Romagnolo, Martina Olivero, et al.
Clinical Immunology (Orlando, Fla.)
|
February 8, 2011
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
Cinzia Mazza, Fabio Buzi, Federica Ortolani, et al.
Page
of 3