Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Giovanna Maione"'
Autor:
Giovanna Maione, Fernanda Iafusco, Angela Zanfardino, Alessia Piscopo, Gulsum Ozen, Dario Iafusco, Nadia Tinto
Publikováno v:
Medicina, Vol 59, Iss 2, p 310 (2023)
In pediatric diabetology, a precise diagnosis is very important because it allows early and correct clinical management of the patient. Monogenic diabetes (MD), which accounts for 1–6% of all pediatric–adolescent diabetes cases, is the most relev
Externí odkaz:
https://doaj.org/article/6ceea73b8d7344358179c08bd03b19f1
Autor:
Fernanda Iafusco, Giovanna Maione, Cristina Mazzaccara, Francesca Di Candia, Enza Mozzillo, Adriana Franzese, Nadia Tinto
Publikováno v:
Diagnostics, Vol 11, Iss 7, p 1164 (2021)
Monogenic diabetes (MD) represents a heterogeneous group of disorders whose most frequent form is maturity-onset diabetes of the young (MODY). MD is predominantly caused by a mutation in a single gene. We report a case of a female patient with suspec
Externí odkaz:
https://doaj.org/article/dfdd5e17f05b4e8d864285fa614b3d16
Autor:
Fernanda Iafusco, Giovanna Maione, Francesco Maria Rosanio, Enza Mozzillo, Adriana Franzese, Nadia Tinto
Publikováno v:
Diagnostics, Vol 11, Iss 3, p 572 (2021)
Cystic fibrosis (CF) is the most common autosomal recessive disease in the Caucasian population and is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that encodes for a chloride/bicarbonate channel expressed on the memb
Externí odkaz:
https://doaj.org/article/7657bf15e06543f389dd1353da6d35da
Autor:
Dario Iafusco, Angela Zanfardino, Alessia Piscopo, Stefano Curto, Alda Troncone, Antonietta Chianese, Assunta Serena Rollato, Veronica Testa, Fernanda Iafusco, Giovanna Maione, Alessandro Pennarella, Lucia Boccabella, Gulsum Ozen, Pier Luigi Palma, Cristina Mazzaccara, Nadia Tinto, Emanuele Miraglia del Giudice
Publikováno v:
International journal of environmental research and public health. 19(5)
Wolfram Syndrome (WS) is a very rare genetic disorder characterized by several symptoms that occur from childhood to adulthood. Usually, the first clinical sign is non-autoimmune diabetes even if other clinical features (optic subatrophy, neurosensor
Autor:
Giovanna Maione, Carola Giacobbe, M.D. Di Taranto, Gabriella Iannuzzo, G. Cardiero, Giuliana Fortunato, Daniela De Palma, Paolo Rubba, Francesco Forte
Publikováno v:
Atherosclerosis. 315:e45-e46
Autor:
Giovanna Maione, Francesca Di Candia, Fernanda Iafusco, Adriana Franzese, Enza Mozzillo, Nadia Tinto, Cristina Mazzaccara
Publikováno v:
Diagnostics, Vol 11, Iss 1164, p 1164 (2021)
Diagnostics
Diagnostics
Monogenic diabetes (MD) represents a heterogeneous group of disorders whose most frequent form is maturity-onset diabetes of the young (MODY). MD is predominantly caused by a mutation in a single gene. We report a case of a female patient with suspec
Autor:
Carola Giacobbe, Ilenia Calcaterra, Giovanna Maione, M.D. Di Taranto, Alessio Buonaiuto, M. N. D. Di Minno, Giuliana Fortunato, Daniela De Palma, G. Cardiero, Paolo Rubba, Gabriella Iannuzzo
Publikováno v:
Atherosclerosis. 315:e207
Autor:
Gabriella Iannuzzo, Giovanna Maione, Ilenia Calcaterra, Giuliana Fortunato, Alessio Buonaiuto, Matteo Nicola Dario Di Minno, Carola Giacobbe, Daniela De Palma, Maria Donata Di Taranto, Paolo Rubba
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 1, p 219 (2020)
Volume 9
Issue 1
Journal of Clinical Medicine, Vol 9, Iss 1, p 219 (2020)
Volume 9
Issue 1
Homozygous familial hypercholesterolemia (HoFH), the severest form of familial hypercholesterolemia (FH), is characterized by very high LDL-cholesterol levels and a high frequency of coronary heart disease. The disease is caused by the presence of ei