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Mariella Valenzise

Showing results (1-10 of 93) with videos related to

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Expert Review of Clinical Pharmacology|November 13, 2018
Controversies in the pharmacological treatment of Graves' disease in childrenFilippo De Luca, Mariella Valenzise
Italian Journal of Pediatrics|August 9, 2017
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric ageMariella Valenzise, Tommaso Aversa, Angiola Saccomanno, et al.
BMJ Case Reports|June 21, 2011
Iatrogenic Cushing syndrome caused by ocular glucocorticoids in a childMaria Francesca Messina, Mariella Valenzise, Salvatore Aversa, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 25, 2020
The evolution of allergen-specific immunotherapy: The near and far futureGiovanni Battista Pajno, Stefano Passanisi, Mariella Valenzise, et al.
Pediatrics|March 6, 2016
Flecainide-Responsive Myotonia Permanens With SNEL Onset: A New Case and Literature ReviewSimona Portaro, Carmelo Rodolico, Stefano Sinicropi, et al.
International Journal of Environmental Research and Public Health|January 11, 2022
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1Giuseppina Salzano, Luciana Rigoli, Mariella Valenzise, et al.
Italian Journal of Pediatrics|March 23, 2018
Epidemiological and clinical aspects of autoimmune thyroid diseases in children with Down's syndromeTommaso Aversa, Giuseppe Crisafulli, Giuseppina Zirilli, et al.
Vaccine|August 31, 2014
Post vaccine acute disseminated encephalomyelitis as the first manifestation of chromosome 22q11.2 deletion syndrome in a 15-month old baby: a case reportMariella Valenzise, Antonio Cascio, Malgorzata Wasniewska, et al.
Italian Journal of Pediatrics|March 5, 2017
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in childrenMariella Valenzise, Tommaso Aversa, Giuseppina Salzano, et al.
Gene|March 28, 2012
Identification of two novel mutations in the first Sicilian APECED patient with no R203X mutation in AIRE gene and review of Italian APECED genotypesMariella Valenzise, Malgorzata Wasniewska, Silvestro Mirabelli, et al.
Pageof 10

Showing results (1-10 of 93) with videos related to

Sort By:
Pageof 10
Expert Review of Clinical Pharmacology|November 13, 2018
Controversies in the pharmacological treatment of Graves' disease in childrenFilippo De Luca, Mariella Valenzise
Italian Journal of Pediatrics|August 9, 2017
Epidemiological and clinical peculiarities of polyglandular syndrome type 3 in pediatric ageMariella Valenzise, Tommaso Aversa, Angiola Saccomanno, et al.
BMJ Case Reports|June 21, 2011
Iatrogenic Cushing syndrome caused by ocular glucocorticoids in a childMaria Francesca Messina, Mariella Valenzise, Salvatore Aversa, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 25, 2020
The evolution of allergen-specific immunotherapy: The near and far futureGiovanni Battista Pajno, Stefano Passanisi, Mariella Valenzise, et al.
Pediatrics|March 6, 2016
Flecainide-Responsive Myotonia Permanens With SNEL Onset: A New Case and Literature ReviewSimona Portaro, Carmelo Rodolico, Stefano Sinicropi, et al.
International Journal of Environmental Research and Public Health|January 11, 2022
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1Giuseppina Salzano, Luciana Rigoli, Mariella Valenzise, et al.
Italian Journal of Pediatrics|March 23, 2018
Epidemiological and clinical aspects of autoimmune thyroid diseases in children with Down's syndromeTommaso Aversa, Giuseppe Crisafulli, Giuseppina Zirilli, et al.
Vaccine|August 31, 2014
Post vaccine acute disseminated encephalomyelitis as the first manifestation of chromosome 22q11.2 deletion syndrome in a 15-month old baby: a case reportMariella Valenzise, Antonio Cascio, Malgorzata Wasniewska, et al.
Italian Journal of Pediatrics|March 5, 2017
Novel insight into Chronic Inflammatory Demyelinating Polineuropathy in APECED syndrome: molecular mechanisms and clinical implications in childrenMariella Valenzise, Tommaso Aversa, Giuseppina Salzano, et al.
Gene|March 28, 2012
Identification of two novel mutations in the first Sicilian APECED patient with no R203X mutation in AIRE gene and review of Italian APECED genotypesMariella Valenzise, Malgorzata Wasniewska, Silvestro Mirabelli, et al.
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