Syrén ML - Search Results

1

Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndrome.

Syrén ML, Tedeschi S, Cesareo L, Bellantuono R, Colussi G, Procaccio M, Alì A, Domenici R, Malberti F, Sprocati M, Sacco M, Miglietti N, Edefonti A, Sereni F, Casari G, Coviello DA, Bettinelli A. Syrén ML, et al. Hum Mutat. 2002 Jul;20(1):78. doi: 10.1002/humu.9045. Hum Mutat. 2002. PMID: 12112667

2

Increased renal tubular Na-K-ATPase activity in Milan hypertensive rats in the prehypertensive period.

Melzi ML, Syrén ML, Assael BM, Sereni F, Aperia A. Melzi ML, et al. Among authors: syren ml. Pediatr Nephrol. 1991 Nov;5(6):700-3. doi: 10.1007/BF00857877. Pediatr Nephrol. 1991. PMID: 1662981

3

Regulation of sodium-potassium-adenosine-triphosphatase activity by extracellular guanosine 3', 5'-cyclic monophosphate in rat kidney.

Syrén ML, Tirelli AS, Assael BM, Sereni F. Syrén ML, et al. Acta Physiol Scand. 1996 Nov;158(3):295-6. doi: 10.1046/j.1365-201X.1996.546314000.x. Acta Physiol Scand. 1996. PMID: 8931773 No abstract available.

4

Phenotypic variability in Bartter syndrome type I.

Bettinelli A, Ciarmatori S, Cesareo L, Tedeschi S, Ruffa G, Appiani AC, Rosini A, Grumieri G, Mercuri B, Sacco M, Leozappa G, Binda S, Cecconi M, Navone C, Curcio C, Syren ML, Casari G. Bettinelli A, et al. Among authors: syren ml. Pediatr Nephrol. 2000 Sep;14(10-11):940-5. doi: 10.1007/pl00013418. Pediatr Nephrol. 2000. PMID: 10975303

5

Bartter syndrome type 3: an unusual cause of nephrolithiasis.

Colussi G, De Ferrari ME, Tedeschi S, Prandoni S, Syrén ML, Civati G. Colussi G, et al. Among authors: syren ml. Nephrol Dial Transplant. 2002 Mar;17(3):521-3. doi: 10.1093/ndt/17.3.521. Nephrol Dial Transplant. 2002. PMID: 11865110 No abstract available.

6

Cardiac arrhythmias due to severe hypokalemia in a patient with classic Bartter disease.

Malafronte C, Borsa N, Tedeschi S, Syrèn ML, Stucchi S, Bianchetti MG, Achilli F, Bettinelli A. Malafronte C, et al. Among authors: syren ml. Pediatr Nephrol. 2004 Dec;19(12):1413-5. doi: 10.1007/s00467-004-1611-0. Pediatr Nephrol. 2004. PMID: 15338397

7

Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome.

Bettinelli A, Borsa N, Syrén ML, Mattiello C, Coviello D, Edefonti A, Giani M, Travi M, Tedeschi S. Bettinelli A, et al. Among authors: syren ml. Pediatr Res. 2005 Dec;58(6):1269-73. doi: 10.1203/01.pdr.0000185267.95466.41. Pediatr Res. 2005. PMID: 16306206

8

Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome.

Vezzoli G, Arcidiacono T, Paloschi V, Terranegra A, Biasion R, Weber G, Mora S, Syren ML, Coviello D, Cusi D, Bianchi G, Soldati L. Vezzoli G, et al. Among authors: syren ml. J Nephrol. 2006 Jul-Aug;19(4):525-8. J Nephrol. 2006. PMID: 17048213

9

Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome.

Bettinelli A, Borsa N, Bellantuono R, Syrèn ML, Calabrese R, Edefonti A, Komninos J, Santostefano M, Beccaria L, Pela I, Bianchetti MG, Tedeschi S. Bettinelli A, et al. Among authors: syren ml. Am J Kidney Dis. 2007 Jan;49(1):91-8. doi: 10.1053/j.ajkd.2006.10.001. Am J Kidney Dis. 2007. PMID: 17185149

10

A thiazide test for the diagnosis of renal tubular hypokalemic disorders.

Colussi G, Bettinelli A, Tedeschi S, De Ferrari ME, Syrén ML, Borsa N, Mattiello C, Casari G, Bianchetti MG. Colussi G, et al. Among authors: syren ml. Clin J Am Soc Nephrol. 2007 May;2(3):454-60. doi: 10.2215/CJN.02950906. Epub 2007 Mar 14. Clin J Am Soc Nephrol. 2007. PMID: 17699451

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