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Nicola Improda

Showing results (11-20 of 39) with videos related to

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Italian Journal of Pediatrics|June 4, 2014
Effect of long-term GH treatment in a patient with CHARGE associationAndrea Esposito, Maria Tufano, Iolanda Di Donato, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 23, 2017
HYDROCORTISONE THERAPY AND GROWTH TRAJECTORY IN CHILDREN WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIACarla Bizzarri, Nicola Improda, Chiara Maggioli, et al.
Italian Journal of Pediatrics|September 22, 2012
Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a childNicola Improda, Maria Alessio, Donatella Capalbo, et al.
Hormone Research in Paediatrics|March 31, 2017
Intrafamilial Phenotypic Variability and Consequences of Non-Compliance with Treatment in Congenital Adrenal Hyperplasia and Congenital Hypothyroidism within a Single Family
Nicola Improda, Caroline Ponmani, Nadia Schoenmakers, et al.
Hormone Research in Paediatrics|June 2, 2016
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical PhenotypeNicola Improda, Pratik Shah, Maria Güemes, et al.
Hormone Research in Paediatrics|June 22, 2026
Cerebral X-Linked Adrenoleukodystrophy Associated with Hemophilia A: a case reportGaetano Terrone, Simona Fecarotta, Paola Lorello, et al.
Frontiers in Endocrinology|April 14, 2025
Case report: Reversible Fanconi syndrome due to vitamin D deficiency in a patient with epilepsy harbouring a pathogenic variant in the SLC34A1 geneNicola Improda, Francesco Maria Rosanio, Luigi Annicchiarico Petruzzelli, et al.
Italian Journal of Pediatrics|January 22, 2013
Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothersManuela Cerbone, Patrizia Agretti, Giuseppina De Marco, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 2020
Cognitive Function in Children With Idiopathic Subclinical Hypothyroidism: Effects of 2 Years of Levothyroxine TherapyDonatella Capalbo, Sara Alfano, Miriam Polizzi, et al.
Italian Journal of Pediatrics|September 22, 2012
Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutationDonatella Capalbo, Maria Giuseppa Scala, Daniela Melis, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Italian Journal of Pediatrics|June 4, 2014
Effect of long-term GH treatment in a patient with CHARGE associationAndrea Esposito, Maria Tufano, Iolanda Di Donato, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|February 23, 2017
HYDROCORTISONE THERAPY AND GROWTH TRAJECTORY IN CHILDREN WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIACarla Bizzarri, Nicola Improda, Chiara Maggioli, et al.
Italian Journal of Pediatrics|September 22, 2012
Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a childNicola Improda, Maria Alessio, Donatella Capalbo, et al.
Hormone Research in Paediatrics|March 31, 2017
Intrafamilial Phenotypic Variability and Consequences of Non-Compliance with Treatment in Congenital Adrenal Hyperplasia and Congenital Hypothyroidism within a Single Family
Nicola Improda, Caroline Ponmani, Nadia Schoenmakers, et al.
Hormone Research in Paediatrics|June 2, 2016
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical PhenotypeNicola Improda, Pratik Shah, Maria Güemes, et al.
Hormone Research in Paediatrics|June 22, 2026
Cerebral X-Linked Adrenoleukodystrophy Associated with Hemophilia A: a case reportGaetano Terrone, Simona Fecarotta, Paola Lorello, et al.
Frontiers in Endocrinology|April 14, 2025
Case report: Reversible Fanconi syndrome due to vitamin D deficiency in a patient with epilepsy harbouring a pathogenic variant in the SLC34A1 geneNicola Improda, Francesco Maria Rosanio, Luigi Annicchiarico Petruzzelli, et al.
Italian Journal of Pediatrics|January 22, 2013
Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothersManuela Cerbone, Patrizia Agretti, Giuseppina De Marco, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 2020
Cognitive Function in Children With Idiopathic Subclinical Hypothyroidism: Effects of 2 Years of Levothyroxine TherapyDonatella Capalbo, Sara Alfano, Miriam Polizzi, et al.
Italian Journal of Pediatrics|September 22, 2012
Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutationDonatella Capalbo, Maria Giuseppa Scala, Daniela Melis, et al.
Pageof 4