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Showing page 1 of results 1 - 10 of about 26 pages

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Growth Trajectory and Final Height in Children with Non Classical Congenital Adrenal Hyperplasia | ESPE2019
Malgorzata Wasniewska; Letteria Anna Morabito; Federico Baronio; Silvia Einaudi; Maria Carolina Salerno; Carla Bizzarri; Gianni
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-300
Published: 2019-08-22

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Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry | ESPE2019
Uta Neumann; der Linde Annelieke van; Ruth Krone; Ayla Guven; Tülay Güran; Heba Elsedfy; Feyza Darendeliler; Tania Bachega; An
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-157
Published: 2019-08-22

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Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds. | ESPE2019
Giuseppa Patti; Saverio Scianguetta; Antonio Balsamo; Marco Cappa; Sabrina Corbetta; Rossella Gaudino; Lorenzo Iughetti; Maria C
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-97
Published: 2019-08-22

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Growth Trajectory and Final Height in Children with Non Classical Congenital Adrenal Hyperplasia | ESPE2019
Malgorzata Wasniewska; Letteria Anna Morabito; Federico Baronio; Silvia Einaudi; Maria Carolina Salerno; Carla Bizzarri; Gianni
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-300.html
Published: 2019-08-22

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Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry | ESPE2019
Uta Neumann; der Linde Annelieke van; Ruth Krone; Ayla Guven; Tülay Güran; Heba Elsedfy; Feyza Darendeliler; Tania Bachega; An
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-157.html
Published: 2019-08-22

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Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds. | ESPE2019
Giuseppa Patti; Saverio Scianguetta; Antonio Balsamo; Marco Cappa; Sabrina Corbetta; Rossella Gaudino; Lorenzo Iughetti; Maria C
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-97.html
Published: 2019-08-22

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Unusual Clinical Presentation of Autoimmune Polyendocrinopathy Type 1 | ESPE2018
Federico Baronio; Rita Ortolano; Simona Ferrari; Alessandra Cassio; Giulio Maltoni; Giacomo Tonti; Antonio Balsamo
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p267.htm
Published: 2018-08-28

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Quantitative Ultrasound Evaluation in a Cohort of 43 Young Adults with Classical CAH due to 21-Hydroxylase Deficiency (21OHD): Is Bone Mineral Quality Impaired? | ESPE2018
Federico Baronio; Antonio Balsamo; Rita Ortolano; Nicoletta Massaccesi; Ilaria Bettocchi; Maximiliano Zioutas; Giulio Maltoni; S
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p033.htm
Published: 2018-08-28

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Genotyping Patients with Differences of Sex Development: 25 Years of Investigation of an Italian Population of 308 Cases (194 46,XY and 114 46,XX) | ESPE2016
Lilia Baldazzi; Soara Menabo; Federico Baronio; Rita Ortolano; Alessandra Cassio; Laura Mazzanti; Antonio Balsamo
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p364.htm
Published: 2016-08-19

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A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH - On Behalf of the I-CAH/I-DSD Registry User Group | ESPE2016
Mariam Kourime; Jillian Bryce; Jipu Jiang; Nayananjani Karunasena; Tulay Guran; Sabine Elisabeth Hannema; Martine Cools; Der Gri
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p356.htm
Published: 2016-08-19

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