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Alberto Bettinelli

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Pediatric Research|November 25, 2005
Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndromeAlberto Bettinelli, Nicolò Borsa, Marie-Louise Syrén, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 26, 2014
Urinary exosomes in the diagnosis of Gitelman and Bartter syndromesSamuele Corbetta, Francesca Raimondo, Silvana Tedeschi, et al.
The American Journal of Medicine|April 6, 2004
Normal plasma total magnesium in Gitelman syndromeFederica Tosi, Nicola D F Bianda, Anita C Truttmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 3, 2010
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestorMarie-Louise Syrén, Nicolò Borsa Ghiringhelli, Alberto Bettinelli, et al.
Italian Journal of Pediatrics|December 15, 2010
Body fluids and salt metabolism - part IIMattia Peruzzo, Gregorio P Milani, Luca Garzoni, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2000
Nephrogenic diabetes insipidus: functional analysis of new AVPR2 mutations identified in Italian familiesElena Albertazzi, Deborah Zanchetta, Pascaline Barbier, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 19, 2007
A thiazide test for the diagnosis of renal tubular hypokalemic disordersGiacomo Colussi, Alberto Bettinelli, Silvana Tedeschi, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2013
Transient benign hyperphophatasemiaGianluca Gualco, Sebastiano A G Lava, Luca Garzoni, et al.
Italian Journal of Pediatrics|September 6, 2013
Symptomatic fever management among 3 different groups of pediatricians in Northern Lombardy (Italy): results of an explorative cross-sectional surveyAlberto Bettinelli, Maria Cristina Provero, Felice Cogliati, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 23, 2006
Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcomeAlberto Bettinelli, Nicolò Borsa, Rosa Bellantuono, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Pediatric Research|November 25, 2005
Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndromeAlberto Bettinelli, Nicolò Borsa, Marie-Louise Syrén, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 26, 2014
Urinary exosomes in the diagnosis of Gitelman and Bartter syndromesSamuele Corbetta, Francesca Raimondo, Silvana Tedeschi, et al.
The American Journal of Medicine|April 6, 2004
Normal plasma total magnesium in Gitelman syndromeFederica Tosi, Nicola D F Bianda, Anita C Truttmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 3, 2010
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestorMarie-Louise Syrén, Nicolò Borsa Ghiringhelli, Alberto Bettinelli, et al.
Italian Journal of Pediatrics|December 15, 2010
Body fluids and salt metabolism - part IIMattia Peruzzo, Gregorio P Milani, Luca Garzoni, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2000
Nephrogenic diabetes insipidus: functional analysis of new AVPR2 mutations identified in Italian familiesElena Albertazzi, Deborah Zanchetta, Pascaline Barbier, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 19, 2007
A thiazide test for the diagnosis of renal tubular hypokalemic disordersGiacomo Colussi, Alberto Bettinelli, Silvana Tedeschi, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2013
Transient benign hyperphophatasemiaGianluca Gualco, Sebastiano A G Lava, Luca Garzoni, et al.
Italian Journal of Pediatrics|September 6, 2013
Symptomatic fever management among 3 different groups of pediatricians in Northern Lombardy (Italy): results of an explorative cross-sectional surveyAlberto Bettinelli, Maria Cristina Provero, Felice Cogliati, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 23, 2006
Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcomeAlberto Bettinelli, Nicolò Borsa, Rosa Bellantuono, et al.
Pageof 5