Zobrazeno 1 - 10
of 350
pro vyhledávání: '"C, Salpietro"'
Autor:
L, Colavita, U, Cucinotta, F, Galletta, R, Chimenz, G, Nicocia, N, Giannitto, G, Ceravolo, M, Sturiale, A, Ceravolo, C, Salpietro, C, Cuppari
Publikováno v:
Journal of biological regulators and homeostatic agents. 34(4 Suppl. 2)
Autor:
C, Cuppari, G, Ceravolo, M D, Ceravolo, S, Sestito, G, Nicocia, R, Chimenz, C, Salpietro, M P, Calabrò
Publikováno v:
Journal of biological regulators and homeostatic agents. 34(4 Suppl. 2)
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first described in a cluster of patients in Wuhan, China, in December of 2019. Over the past few months, COVID-19 has rapidly spread worl
Autor:
C, Cuppari, M, Amatruda, G, Ceravolo, M D, Ceravolo, L, Oreto, L, Colavita, A, Barbalace, M P, Calabrò, C, Salpietro
Publikováno v:
Journal of biological regulators and homeostatic agents. 34(4 Suppl. 2)
Autor:
M, Amatruda, M D, Ceravolo, G, Ceravolo, C, Cuppari, L, Oreto, B, Piraino, F, Xerra, G, Nicocia, C, Salpietro, M P, Calabrò
Publikováno v:
Journal of biological regulators and homeostatic agents. 34(4 Suppl. 2)
Childhood obesity is the "disease of the century". This article reviews the early cardiovascular risk factors and the recommendations to prevent them in the overweight and obese children. A comprehensive search of published literature was carried out
Autor:
I, Loddo, F, Barbera, G, Di Gesaro, M C, Cutrupi, M P, Calabrò, G, Ceravolo, C, Salpietro, S M C, Gramaglia, A, Ceravolo, D, Concolino, R, De Sarro, C, Cuppari, E, Gitto, F, Clemenza, D, Di Carlo
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::295b1f86c99b7887f77da4ecf40c5cc5
https://hdl.handle.net/11570/3184493
https://hdl.handle.net/11570/3184493
Autor:
S. Gangemi, A. Saija, A. Tomaino, F. Cimino, R. A. Merendino, P. L. Minciullo, S. Briuglia, M. V. Merlino, B. Dallapiccola, B. Ferlazzo, D. C. Salpietro
Publikováno v:
Mediators of Inflammation, Vol 12, Iss 4, Pp 247-249 (2003)
Familiar chronic nail candidiasis (FCNC) is a rare disorder characterized by early-onset infections caused by different species of Candida, restricted to the nail of the hands and feet, and associated with a low serum concentration of intercellular a
Externí odkaz:
https://doaj.org/article/fd16a2e871a84679906ede48276f5572
Autor:
L, Colavita, C, Salpietro, C, Cuppari, A, Sallemi, V, Di Benedetto, D, Concolino, L, Marseglia, G, D'Angelo, E, Gitto, P, Betta, C, Fede, G, Conti, R, Chimenz
Nephrotic Syndrome (NS) is a rare diseases (around 2-7 cases per 100.000 children per year) characterized by proteinuria ≥50 mg/kg/day (or ≥40 mg/m2/h) or a proteinuria/creatininuria ratio2 (mg/mg); hypoalbuminaemia less than 25 g/l and edema. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c339ac3f8f41c4d9df0aabc736dc7f77
http://hdl.handle.net/20.500.11769/371101
http://hdl.handle.net/20.500.11769/371101
Autor:
S, Passanisi, G, D'Angelo, L, Marseglia, C, De Cola, R, Granese, G, Conti, P, Betta, M C, Cutrupi, C, Fede, R, Chimenz, C, Salpietro, E, Gitto
Nocturnal enuresis (NE) was defined by the World Health Organization (ICD-10) and the American Psychiatric Association (DSM-5) as bed-wetting in children aged5 years. In cases of mental retardation, the developmental age may be equivalent to 5 years.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0b3167ca58a937af00826455613586ce
http://hdl.handle.net/11570/3147128
http://hdl.handle.net/11570/3147128
Autor:
Antonio Novelli, M V Merlino, Rita Mingarelli, Silvana Briuglia, Bruno Dallapiccola, Laura Bernardini, D. C. Salpietro
Publikováno v:
American Journal of Medical Genetics. :165-169
A 46,XYq 8-year-old male was referred for microcephaly, growth, and mental retardation, hypotonia, genital hypoplasia, and dysmorphisms. FISH analysis showed that the rearranged Y chromosome originated from an unbalanced translocation of Xq27.3-qter
Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay
Autor:
Alessia Colosimo, Chiara Di Bella, Silvana Briuglia, Valentina Guida, Luciana Rigoli, Liborio Stuppia, Bruno Dallapiccola, D. C. Salpietro, Alessandro De Luca
Publikováno v:
Human Mutation. 21:622-629
Wolfram syndrome (WS) is a recessively inherited mendelian form of diabetes and neurodegeneration also known by the acronym DIDMOAD from the major clinical features, including diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Affect