Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M C Cutrupi"'
Autor:
Caterina Cuppari, Roberto Chimenz, M D Ceravolo, Celeste Casto, Gianluca Piccolo, Remo Albiero, Alessio Mancuso, Antonella Gambadauro, Valeria Dipasquale, Paola Borgia, G Ceravolo, Maria Pia Calabrò, M C Cutrupi, Tommaso La Macchia
Publikováno v:
Children
Children, Vol 8, Iss 528, p 528 (2021)
Children, Vol 8, Iss 528, p 528 (2021)
Cardiorenal syndrome (CRS) is defined as a disorder resulting from the abnormal interaction between the heart and kidney, in which acute or chronic dysfunction of one organ may lead to acute and/or chronic dysfunction of the other. The functional int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a922a6619dc06d36f13742c30c35ebf
http://hdl.handle.net/11570/3212024
http://hdl.handle.net/11570/3212024
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:
G. Ganci, M C Cutrupi, Sebastiano Gangemi, Marco Casciaro, Caterina Cuppari, Sara Manti, R. Chimenz, E. Di Salvo, V. Procopio, Carmelo Salpietro
Publikováno v:
Clinical Genetics. 94:81-94
Familial Mediterranean fever (FMF) is the most common autosomal recessive autoinflammatory disease. To date, following the isolation of more than 280 MEFV sequence variants, the genotype-phenotype correlation in FMF patients has been intensively inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c528d79517f589b5d2a1088c9fc98f7
https://doi.org/10.1111/cge.13223
https://doi.org/10.1111/cge.13223
Autor:
M. A. La Rosa, Vincenzo Salpietro, Caterina Cuppari, M C Cutrupi, Valeria Dipasquale, Elisa Ferro, G. Di Rosa, Roberto Chimenz, A. Valenti, Sara Manti
Publikováno v:
Journal of Intellectual Disability Research. 62:382-390
Background Intellectual disability (ID) is part of the Down syndrome (DS) phenotypic spectrum, but the exact molecular pathophysiology of ID in individuals with DS is not yet fully understood, with many research hypotheses still unproven. Basing on p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36554c3fc68db9edc02b31c23e518c32
https://doi.org/10.1111/jir.12470
https://doi.org/10.1111/jir.12470
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:
V. Procopio, F. Maimone, M C Cutrupi, Carmelo Salpietro, Sara Manti, Giovanni Conti, G. Bianco, Caterina Cuppari, T. Arrigo, Anna Claudia Romeo
Publikováno v:
Gene. 641
Background Uncertainty remains on the pathogenetic mechanisms, model of inheritance as well as genotype-phenotype correlation of FMF disease. Objective To investigate the impact of genetic factors on the FMF phenotype and the disease inheritance mode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038ef866c29c0128a54568c05f724321
https://pubmed.ncbi.nlm.nih.gov/29080837
https://pubmed.ncbi.nlm.nih.gov/29080837
Autor:
Manuela Baronio, M C Cutrupi, Vincenzo Salpietro, Daniele Moratto, Silvana Briuglia, Vassilios Lougaris, Alessandro Plebani, Kshitij Mankad, Carmelo Salpietro, M. R. Pizzino
Publikováno v:
Orphanet Journal of Rare Diseases
Proteus syndrome (PS) is an extremely rare and complex disease characterized by malformations and overgrowth of different tissues. Prognosis of affected patients may be complicated by premature death, mostly due to pulmonary embolism and respiratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::895b84b2958705832c021221bf9be531
http://hdl.handle.net/11567/981654
http://hdl.handle.net/11567/981654
Autor:
Teresa Arrigo, Caterina Cuppari, Valeria Chirico, Antonio David, Antonio Lacquaniti, L. Grasso, Carmelo Salpietro, Luciana Rigoli, Basilia Piraino, M C Cutrupi
Summary High mobility group box -1 (HMGB1) represents a common causal agent for various types of diseases, including infective pathologies. This study aimed to investigate the role of HMGB1 in β-thalassemia major (TM) by evaluating its diagnostic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d5cd6b38a220d54ac460bd0e2effdf
http://hdl.handle.net/11570/3091974
http://hdl.handle.net/11570/3091974