Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cinzia, Chiaramonte"'
Autor:
Ingrid Anne Mandy Schierz, Mario Giuffrè, Mariaserena Lo Presti, Giuseppa Pinello, Cinzia Chiaramonte, Enrica Maria Agosta Cecala, Giovanni Corsello
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 8, Iss C, Pp 10-12 (2016)
Gastrointestinal perforation (GIP) in preterm neonates may be idiopathic, due to necrotizing enterocolitis (NEC), or mechanical obstruction. The predominant cause of GIP in the neonatal period is NEC. Differential diagnosis with congenital malformati
Externí odkaz:
https://doaj.org/article/b4aa4594a4b8413b9f14f2963348a04d
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
Externí odkaz:
https://doaj.org/article/13b910a8cee84003969d20c27ae6ee1a
Publikováno v:
Urology Case Reports, Vol 2, Iss 2, Pp 67-69 (2014)
Splenogonadal fusion is a rare congenital anomaly in which there is fusion between the spleen and gonad, epididymis or vas. We treated a patient with scrotal mass. A discontinuous fusion between the spleen and epididymis was found: after frozen secti
Externí odkaz:
https://doaj.org/article/cd8a2c5e4dad4f4c8e2ff6b24429e291
Autor:
Chiara Tudisca, Maria Chiara Terranova, Cinzia Chiaramonte, Giuseppe Lo Re, Giuseppe Li Voti, Sergio Salerno
Publikováno v:
Gazzetta Medica Italiana Archivio per le Scienze Mediche. 179
Congenital anomalies of kidney and urinary tract (CAKUT) occur in up to 3.2% of infants, and in almost one third of cases they are associated to genital aberrations. DMSA renal scintigraphy is considered the gold standard in CAKUT patients, to assess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4febce66dd1e0082627af6e2b4febcb2
https://doi.org/10.23736/s0393-3660.19.04056-7
https://doi.org/10.23736/s0393-3660.19.04056-7
Autor:
Elisa, Zambaiti1, Cinzia, Chiaramonte1, Sergio, Salerno2, Giuseppe, Li Voti1, Fortunato, Siracusa1
Publikováno v:
Case Reports in Pediatrics. 3/15/2016, p1-4. 4p.
Autor:
Flavia Tripi, F. Cataliotti, Elettra Vestri, Cinzia Chiaramonte, Antonino Giulio Giannone, Marcello Cimador
Background Female vaginoplasty reconstruction, by choice, is usually performed with adjacent tissue. However in some clinical conditions such as high urogenital confluence sinus, cloacal malformation with extreme vaginal hypoplasia, local tissue may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7dfe91ab21343f91498910e31913c2b
http://hdl.handle.net/10447/403051
http://hdl.handle.net/10447/403051
Publikováno v:
Urology. 95
Objective To highlight genetic pattern of posterior urethral valves (PUVs), we performed a genetic study on 2 siblings affected. PUVs are the most common congenital cause of lower urinary tract obstruction and an important cause of renal failure in i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8835467df1cbcbc2629c62e678b9d9b
https://pubmed.ncbi.nlm.nih.gov/27261184
https://pubmed.ncbi.nlm.nih.gov/27261184
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
In the article titled “Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation” [1], the authors' first and last names were reversed. The correct author list is shown above.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d16d9b5aebc045e5984c2b648903fe
https://doi.org/10.1155/2016/5353012
https://doi.org/10.1155/2016/5353012