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Marco Cappa

Showing results (171-180 of 207) with videos related to

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Human Vaccines & Immunotherapeutics|November 18, 2015
Streptococcus pneumoniae oropharyngeal colonization in school-age children and adolescents with type 1 diabetes mellitus: Impact of the heptavalent pneumococcal conjugate vaccineNicola Principi, Lorenzo Iughetti, Marco Cappa, et al.
Frontiers in Immunology|July 17, 2023
Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathiesGiorgia Paldino, Maria Felicia Faienza, Marco Cappa, et al.
International Journal of Molecular Sciences|December 11, 2022
Biallelic Inactivating <i>TUB</i> Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary CiliumLucia Ziccardi, Marcello Niceta, Emilia Stellacci, et al.
Frontiers in Endocrinology|October 5, 2020
Summary of Expert Opinion on the Management of Children With Chronic Kidney Disease and Growth Failure With Human Growth HormoneMarco Cappa, Mohamad Maghnie, Vincenza Carbone, et al.
European Journal of Endocrinology|June 8, 2011
Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarcheLucia Ghizzoni, Marco Cappa, Alessandra Vottero, et al.
Clinical Endocrinology|January 15, 2013
Central adrenal insufficiency in young adults with Prader-Willi syndromeGraziano Grugni, Luciano Beccaria, Andrea Corrias, et al.
The Journal of Headache and Pain|July 23, 2021
Early alterations of cortical thickness and gyrification in migraine without aura: a retrospective MRI study in pediatric patientsAlessia Guarnera, Francesca Bottino, Antonio Napolitano, et al.
European Journal of Endocrinology|March 6, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutationsSilverio Perrotta, Natascia Di Iorgi, Fulvio Della Ragione, et al.
European Journal of Endocrinology|April 2, 2025
Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypesAtilano Carcavilla, Arrate Pereda, Mami Miyado, et al.
Frontiers in Endocrinology|August 1, 2022
Expert Opinion on the Management of Growth Hormone Deficiency in Brain Tumor Survivors: Results From an Italian SurveyNatascia Di Iorgi, Giovanni Morana, Marco Cappa, et al.
Pageof 21

Showing results (171-180 of 207) with videos related to

Sort By:
Pageof 21
Human Vaccines & Immunotherapeutics|November 18, 2015
Streptococcus pneumoniae oropharyngeal colonization in school-age children and adolescents with type 1 diabetes mellitus: Impact of the heptavalent pneumococcal conjugate vaccineNicola Principi, Lorenzo Iughetti, Marco Cappa, et al.
Frontiers in Immunology|July 17, 2023
Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathiesGiorgia Paldino, Maria Felicia Faienza, Marco Cappa, et al.
International Journal of Molecular Sciences|December 11, 2022
Biallelic Inactivating <i>TUB</i> Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary CiliumLucia Ziccardi, Marcello Niceta, Emilia Stellacci, et al.
Frontiers in Endocrinology|October 5, 2020
Summary of Expert Opinion on the Management of Children With Chronic Kidney Disease and Growth Failure With Human Growth HormoneMarco Cappa, Mohamad Maghnie, Vincenza Carbone, et al.
European Journal of Endocrinology|June 8, 2011
Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarcheLucia Ghizzoni, Marco Cappa, Alessandra Vottero, et al.
Clinical Endocrinology|January 15, 2013
Central adrenal insufficiency in young adults with Prader-Willi syndromeGraziano Grugni, Luciano Beccaria, Andrea Corrias, et al.
The Journal of Headache and Pain|July 23, 2021
Early alterations of cortical thickness and gyrification in migraine without aura: a retrospective MRI study in pediatric patientsAlessia Guarnera, Francesca Bottino, Antonio Napolitano, et al.
European Journal of Endocrinology|March 6, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutationsSilverio Perrotta, Natascia Di Iorgi, Fulvio Della Ragione, et al.
European Journal of Endocrinology|April 2, 2025
Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypesAtilano Carcavilla, Arrate Pereda, Mami Miyado, et al.
Frontiers in Endocrinology|August 1, 2022
Expert Opinion on the Management of Growth Hormone Deficiency in Brain Tumor Survivors: Results From an Italian SurveyNatascia Di Iorgi, Giovanni Morana, Marco Cappa, et al.
Pageof 21