Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fabiana, Tammaro"'
Autor:
Elena, Puricelli, Alberto, Bettinelli, Nicolò, Borsa, Francesca, Sironi, Camilla, Mattiello, Fabiana, Tammaro, Silvana, Tedeschi, Mario G, Bianchetti, Aurora, Rossodivita
Publikováno v:
Puricelli, Elena; Bettinelli, Alberto; Borsa, Nicolò; Sironi, Francesca; Mattiello, Camilla; Tammaro, Fabiana; Tedeschi, Silvana; Bianchetti, Mario G (2010). Long-term follow-up of patients with Bartter syndrome type I and II. Nephrology, dialysis, transplantation, 25(9), pp. 2976-2981. Oxford: Oxford University Press 10.1093/ndt/gfq119
BACKGROUND: Little information is available on a long-term follow-up in Bartter syndrome type I and II. METHODS: Clinical presentation, treatment and long-term follow-up (5.0-21, median 11 years) were evaluated in 15 Italian patients with homozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::045f15b85a05ccf177a5349411c8c44d
http://doc.rero.ch/record/303001/files/gfq119.pdf
http://doc.rero.ch/record/303001/files/gfq119.pdf
Autor:
Fabiana Tammaro, Laura Longoni, Mario G. Bianchetti, Luca Garzoni, Pietro B. Faré, Alberto Bettinelli
Publikováno v:
Pediatric Nephrology. 27:733-739
Hypotonic hyponatremia, a serious and recognized complication of any intracranial disorder, results from extra-cellular fluid volume depletion, inappropriate anti-diuresis or renal salt-wasting. The putative mechanisms by which intracranial disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac20be19b23040c19fef7ad42e5352fa
https://doi.org/10.1007/s00467-011-2093-5
https://doi.org/10.1007/s00467-011-2093-5
Autor:
Donatella Cattarelli, Marie Louise Syren, Silvana Tedeschi, Mario G. Bianchetti, Fabiana Tammaro, Alberto Bettinelli, Alessandra Cavazza, Carla Colombo
Publikováno v:
Pediatric nephrology (Berlin, Germany). 25(10)
Inactivating mutations in the SLC12A3 gene that encodes the thiazide-sensitive co-transporter causes Gitelman syndrome. The main features of this syndrome include normal or low blood pressure, hypokalemia, metabolic alkalosis, hypomagnesemia, hypocal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f402e585660ba2a52489c893b5cb4357
https://pubmed.ncbi.nlm.nih.gov/20552229
https://pubmed.ncbi.nlm.nih.gov/20552229
Autor:
Alberto Bettinelli, Maria Caiata-Zufferey, Cinzia Cortesi, Mario G. Bianchetti, Olivier Giannini, Sebastiano A. G. Lava, Fabiana Tammaro
Publikováno v:
Cortesi, Cinzia; Lava, Sebastiano A. G.; Bettinelli, Alberto; Tammaro, Fabiana; Giannini, Olivier; Caiata-Zufferey, Maria; Bianchetti, Mario G. (2010). Cardiac arrhythmias and rhabdomyolysis in Bartter–Gitelman patients. Pediatric nephrology, 25(10), pp. 2005-2008. Springer-Verlag 10.1007/s00467-010-1580-4
Recent data demonstrate that patients affected with hypokalemic salt-losing tubulopathies are prone to acute cardiac arrhythmias and rhabdomyolysis. The tendency to these potentially fatal complications is especially high if chronic hypokalemia is se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::070ccd96664e626c35b2785561f21dbe
Autor:
Fabiana Tammaro, Tiziana Piccolo, Rosa Penza, Lucia Lospalluti, Giovanni Pannarale, E. Bonifazi, Gabriella Aceto, Raffaele Calabrese, Lucrezia Garofalo
Publikováno v:
Pediatric nephrology (Berlin, Germany). 23(1)
Epidermolysis bullosa (EB) consists of a group of dominant or recessive autosomal diseases characterised by skin and mucosa fragility. The lesions leave erosions and scars that, in turn, can cause stenosis of tracheal, oesophageal, and genitourinary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::219540009da103c74dfa179d30c26e73
https://pubmed.ncbi.nlm.nih.gov/17955267
https://pubmed.ncbi.nlm.nih.gov/17955267