Zobrazeno 1 - 10
of 218
pro vyhledávání: '"R, Chimenz"'
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)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec79e09642b195afe3b62e2cea3c6862
https://pubmed.ncbi.nlm.nih.gov/33000602
https://pubmed.ncbi.nlm.nih.gov/33000602
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::408d88ad07842e914d81e344cab26c7c
https://pubmed.ncbi.nlm.nih.gov/33000610
https://pubmed.ncbi.nlm.nih.gov/33000610
Autor:
F, Nascimben, F M, Peri, P, Impellizzeri, R, Chimenz, L, Cannavò, D, Pellegrino, G, Ceravolo, M P, Calabrò, E, Gitto, C, Romeo
Publikováno v:
Journal of biological regulators and homeostatic agents. 34(4 Suppl. 2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::44e2d1dbf210522a3532aa27c3432937
https://pubmed.ncbi.nlm.nih.gov/33000606
https://pubmed.ncbi.nlm.nih.gov/33000606
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
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
G, Stroscio, D, Impollonia, T, Arrigo, A, Sallemi, V, Di Benedetto, M G, Scuderi, M, Fusco, D, Concolino, M, Falsaperla, P, Betta, R, Chimenz
Publikováno v:
Journal of biological regulators and homeostatic agents. 33(5 Suppl. 1)
The purpose of this article is to review the main congenital anomalies of kidneys and urinary tract that can be diagnosed prenatally and postnatally by imaging technique. The incidence of congenital anomalies of the kidney and urinary tract during th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::183cd19de5d61d542477081f345715d2
https://pubmed.ncbi.nlm.nih.gov/31630707
https://pubmed.ncbi.nlm.nih.gov/31630707
Autor:
S, Sestito, F, Falvo, A, Sallemi, M, Petrisano, M G, Scuderi, F, Tarsitano, G, D'Angelo, P, Betta, K, Roppa, F, Parisi, L, Pensabene, C, Fede, R, Chimenz, D, Concolino
Publikováno v:
Journal of biological regulators and homeostatic agents. 33(5 Suppl. 1)
Anderson-Fabry Disease (AFD) is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficient or absent activity of the lysosomal enzyme, α-galactosidase A, resulting in the progressive multisystem lysosomal accumulation of gly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ab8b0dbbdf630941b4f417965dbb457
https://pubmed.ncbi.nlm.nih.gov/31630715
https://pubmed.ncbi.nlm.nih.gov/31630715
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