Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Alberto Bettinelli"'
Publikováno v:
Pediatric Kidney Disease ISBN: 9783031116643
Pediatric Kidney Disease ISBN: 9783662529706
Pediatric Kidney Disease ISBN: 9783662529706
Disturbances involving fluid, electrolyte and acid-base balance are rather common. Very often, more than one disturbance in fluid, electrolyte and acid-base homeostasis concurrently occurs in the same subject. In general, the etiology of fluid, elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::348e0bcc75ebe9135893bbb6da4ad0bb
https://doi.org/10.1007/978-3-031-11665-0_34
https://doi.org/10.1007/978-3-031-11665-0_34
Autor:
Rodo O. von Vigier, Carmen Casaulta Aebischer, Anita C. Truttmann, Alberto Bettinelli, Mario G. Bianchetti, Bendicht Wermuth, Karin Zindler‐Schmocker
Publikováno v:
von Vigier, Rodo O.; Truttmann, Anita C.; Zindler-Schmocker, Karin; Bettinelli, Alberto; Casaulta Aebischer, Carmen; Wermuth, Bendicht; Bianchetti, Mario G. (2000). Aminoglycosides and renal magnesium homeostasis in humans. Nephrology, dialysis, transplantation, 15(6), pp. 822-826. Oxford University Press 10.1093/ndt/15.6.822
complication of aminoglycosides, which is mostly asso- ciated with acute renal failure, has been documented Background. The use of aminoglycosides has been linked with hypomagnesaemia in scattered reports. The in scattered anecdotal reports (1-5). Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d766f5808092e02e6b2c37beafd5d05a
http://doc.rero.ch/record/298748/files/150822.pdf
http://doc.rero.ch/record/298748/files/150822.pdf
Publikováno v:
Peters, N.; Bettinelli, A.; Spicher, I.; Basilico, E.; Metta, M. G.; Bianchetti, M. G. (1995). Renal tubular function in children and adolescents with Gitelnian's syndrome, the hypocalciuric variant of Bartter's syndrome. Nephrology, dialysis, transplantation, 10(8), pp. 1313-1319. Oxford University Press 10.1093/ndt/10.8.1313
Renal tubular function was studied in 14 patients with Gitelman's syndrome and 14 control subjects. Apart from the biochemical hallmarks of Gitelman's syndrome, namely alkalaemia, hyperbi carbonataemia, hypokalaemia, hypomagnesaemia (with increased m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::834e4aaa646ee01a2f4d18fb4b678087
http://doc.rero.ch/record/300401/files/10-8-1313.pdf
http://doc.rero.ch/record/300401/files/10-8-1313.pdf
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:
Alberto Bettinelli, Mario G. Bianchetti, Sebastiano A. G. Lava, Camilla Lavagno, Emilio F. Fossali, Pietro B. Faré, Gregorio P. Milani
Publikováno v:
Journal of Medicine and the Person. 12:68-72
“Problem-based learning” differs from lecture-based teaching because it centers on problems using scenarios to illustrate previously taught material and takes place within a group, where participants contribute to the learning process at every st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7cb81fa8f77a9c5044e83556c1353ae
https://doi.org/10.1007/s12682-014-0179-0
https://doi.org/10.1007/s12682-014-0179-0
Autor:
Barbara Scicchitano, Alessandra Albisetti, Alberto Bettinelli, Cristina Viganò, Maria Cristina Provero, Mario G. Bianchetti, Francesco Barretta, Silvana Tedeschi
Publikováno v:
Pediatric Nephrology. 29:2133-2138
Bartter patients may be hypercalciuric. Additional abnormalities in the metabolism of calcium, phosphate, and calciotropic hormones have occasionally been reported. The metabolism of calcium, phosphate, and calciotropic hormones was investigated in 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f167b3382e77480b25d7ce3e49e0d8
https://doi.org/10.1007/s00467-014-2846-z
https://doi.org/10.1007/s00467-014-2846-z
Autor:
Giacomo D. Simonetti, Mario G. Bianchetti, Alberto Bettinelli, Gianluca Gualco, Luca Garzoni, Sebastiano A. G. Lava, Maria Cristina Provero, Gregorio P. Milani
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 57:167-171
Background and aim Sometimes, a temporary increase in alkaline phosphatase level is found in healthy infants and toddlers without evidence of liver or bone disease. The condition is customarily termed transient benign hyperphosphatasemia of infancy a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7204e10214a9a40bd28da12a34a61aab
https://doi.org/10.1097/mpg.0b013e3182922807
https://doi.org/10.1097/mpg.0b013e3182922807
Autor:
Alberto Bettinelli, Oliver Large, Frances M. Ashcroft, Peter Kotanko, Anita A C Reed, Rayaz A. Malik, Connie Schrander-Stumpel, M. Andrew Nesbit, Noemia P. Goldraich, Bernd Hoppe, Jonathan D. Lippiat, Paul T. Christie, Dvora Rubinger, Karl Lhotta, Bernard Roussel, Fiona Wu, Delphine Morel, Michael J. Dillon, Chantal Loirat, Erkin Serdaroglu, Rajesh V. Thakker, Nellie Y. Loh, Sian Williams
Background/Aims: Dent’s disease is caused by mutations in the chloride/proton antiporter, CLC-5, or oculo-cerebro-renal-syndrome-of-Lowe (OCRL1) genes. Methods: Eighteen probands with Dent’s disease were investigated for mutations in CLC-5 and tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f982b1d761cc0bf01d7c4a439599bbd6
https://ora.ox.ac.uk/objects/uuid:308ee457-811b-4cef-b426-9efa7bc5847e
https://ora.ox.ac.uk/objects/uuid:308ee457-811b-4cef-b426-9efa7bc5847e
Autor:
Ira Davis, Beatrice Goilav, Detlef Bockenhauer, Jeffrey J. Fadrowski, Ben A. Semmekrot, Trevor Cole, Lynn M. Boyden, Shrikant Mane, Margo Whiteford, Robert D. Bjornson, Giacomo Colussi, Tracy E. Hunley, Joseph R. Tucci, Fiona E. Karet, Craig C. Porter, Mohan Shenoy, Murim Choi, Priya Vaidyanathan, John W. Foreman, Jai Radhakrishnan, Stephanie Dewar, Alain Poujol, Sami A. Sanjad, Keith A. Choate, Carol Nelson-Williams, Kim M. Keppler-Noreuil, Richard D. Gordon, Matti Välimäki, Majid Rasoulpour, Richard P. Lifton, Maury Pinsk, Ali G. Gharavi, Craig W. Belsha, Hania Z. Al-Shahrouri, Sudhir K. Anand, Irina Tikhonova, Maria Elisabetta De Ferrari, Jim R. Stockigt, Marcel Lebel, Raoul D. Nelson, Howard Trachtman, Anita Farhi, Michael Gutkin, Alberto Bettinelli, Farook Thameem, Hakan R. Toka
Publikováno v:
Nature
Hypertension affects one billion people and is a principal reversible risk factor for cardiovascular disease. Pseudohypoaldosteronism type II (PHAII), a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis, has reveale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b392806a0877cd37740f1ac637bafa2
https://doi.org/10.1038/nature10814
https://doi.org/10.1038/nature10814
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