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Items: 1 to 50 of 101

1.

Impact of acquisition count statistics reduction and SUV discretization on PET radiomic features in pediatric 18F-FDG-PET/MRI examinations.

Branchini M, Zorz A, Zucchetta P, Bettinelli A, De Monte F, Cecchin D, Paiusco M.

Phys Med. 2019 Mar;59:117-126. doi: 10.1016/j.ejmp.2019.03.005. Epub 2019 Mar 16.

PMID:
30928060
2.

Validity and reliability of Italian version of the Non-Communicating Children's Pain Checklist: revised version.

Murgia M, Izzo R, Bettinelli A, Di Maggio C, De Angelis M, Mangone M, Paoloni M, Bernetti A, Torquati A, Leuzzi V, Santilli V.

Eur J Phys Rehabil Med. 2019 Feb;55(1):89-94. doi: 10.23736/S1973-9087.18.05314-5. Epub 2018 Aug 29.

3.

Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.

Corbetta S, Raimondo F, Tedeschi S, Syrèn ML, Rebora P, Savoia A, Baldi L, Bettinelli A, Pitto M.

Nephrol Dial Transplant. 2015 Apr;30(4):621-30. doi: 10.1093/ndt/gfu362. Epub 2014 Nov 23.

PMID:
25422309
4.

Fever phobia among Italian caregivers: a survey in a pediatric emergency department.

Saettini F, Bettinelli A.

Minerva Pediatr. 2014 Aug;66(4):261-6.

PMID:
25198561
5.

Best practice guidelines for idiopathic nephrotic syndrome: recommendations versus reality.

Pasini A, Aceto G, Ammenti A, Ardissino G, Azzolina V, Bettinelli A, Cama E, Cantatore S, Crisafi A, Conti G, D'Agostino M, Dozza A, Edefonti A, Fede C, Groppali E, Gualeni C, Lavacchini A, Lepore M, Maringhini S, Mariotti P, Materassi M, Mencarelli F, Messina G, Negri A, Piepoli M, Ravaglia F, Simoni A, Spagnoletta L, Montini G; NefroKid Study Group.

Pediatr Nephrol. 2015 Jan;30(1):91-101. doi: 10.1007/s00467-014-2903-7. Epub 2014 Aug 17.

6.

Simulation and optimization models for emergency medical systems planning.

Bettinelli A, Cordone R, Ficarelli F, Righini G.

J Emerg Manag. 2014 Jul-Aug;12(4):287-301. doi: 10.5055/jem.2014.0180.

PMID:
25069023
7.

Phosphate homeostasis in Bartter syndrome: a case-control study.

Bettinelli A, Viganò C, Provero MC, Barretta F, Albisetti A, Tedeschi S, Scicchitano B, Bianchetti MG.

Pediatr Nephrol. 2014 Nov;29(11):2133-8. doi: 10.1007/s00467-014-2846-z. Epub 2014 Jun 6.

PMID:
24902942
8.

Ureteral or vesical involvement in Henoch-Schönlein syndrome: a systematic review of the literature.

Siegenthaler GM, Rizzi M, Bettinelli A, Simonetti GD, Ferrarini A, Bianchetti MG.

Pediatr Nephrol. 2014 Feb;29(2):235-9. doi: 10.1007/s00467-013-2621-6. Epub 2013 Sep 24. Review.

PMID:
24061644
9.

Symptomatic fever management among 3 different groups of pediatricians in Northern Lombardy (Italy): results of an explorative cross-sectional survey.

Bettinelli A, Provero MC, Cogliati F, Villella A, Marinoni M, Saettini F, Bianchetti MG, Nespoli L, Galluzzo C, Lava SA.

Ital J Pediatr. 2013 Sep 2;39:51. doi: 10.1186/1824-7288-39-51.

10.

Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.

Bettinelli AL, Mulder TJ, Funke BH, Lafferty KA, Longo SA, Niyazov DM.

Am J Med Genet A. 2013 Dec;161A(12):3187-90. doi: 10.1002/ajmg.a.36182. Epub 2013 Aug 16.

PMID:
23956225
11.

Transient benign hyperphophatasemia.

Gualco G, Lava SA, Garzoni L, Simonetti GD, Bettinelli A, Milani GP, Provero MC, Bianchetti MG.

J Pediatr Gastroenterol Nutr. 2013 Aug;57(2):167-71. doi: 10.1097/MPG.0b013e3182922807.

PMID:
23539049
12.

Algorithm for parametric community detection in networks.

Bettinelli A, Hansen P, Liberti L.

Phys Rev E Stat Nonlin Soft Matter Phys. 2012 Jul;86(1 Pt 2):016107. Epub 2012 Jul 13.

PMID:
23005491
13.

Renal phosphate handling in Gitelman syndrome--the results of a case-control study.

Viganò C, Amoruso C, Barretta F, Minnici G, Albisetti W, Syrèn ML, Bianchetti MG, Bettinelli A.

Pediatr Nephrol. 2013 Jan;28(1):65-70. doi: 10.1007/s00467-012-2297-3. Epub 2012 Sep 19.

PMID:
22990302
14.

Puberty is associated with increased deterioration of renal function in patients with CKD: data from the ItalKid Project.

Ardissino G, Testa S, Daccò V, Paglialonga F, Viganò S, Felice-Civitillo C, Battaglino F, Bettinelli A, Bordugo A, Cecchetti V, De Pascale S, La Manna A, Li Volti S, Maringhini S, Montini G, Pennesi M, Peratoner L.

Arch Dis Child. 2012 Oct;97(10):885-8. doi: 10.1136/archdischild-2011-300685. Epub 2012 Jul 25.

PMID:
22833407
15.

Living with Gitelman disease: an insight into patients' daily experiences.

Caiata-Zufferey M, Zanini CA, Schulz PJ, Syrén ML, Bianchetti MG, Bettinelli A.

Nephrol Dial Transplant. 2012 Aug;27(8):3196-201. doi: 10.1093/ndt/gfs017. Epub 2012 Feb 14.

PMID:
22334612
16.

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.

Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Välimäki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, Tucci JR, Stockigt JR, Keppler-Noreuil KM, Porter CC, Anand SK, Whiteford ML, Davis ID, Dewar SB, Bettinelli A, Fadrowski JJ, Belsha CW, Hunley TE, Nelson RD, Trachtman H, Cole TR, Pinsk M, Bockenhauer D, Shenoy M, Vaidyanathan P, Foreman JW, Rasoulpour M, Thameem F, Al-Shahrouri HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP.

Nature. 2012 Jan 22;482(7383):98-102. doi: 10.1038/nature10814.

17.

Renal salt-wasting syndrome in children with intracranial disorders.

Bettinelli A, Longoni L, Tammaro F, Faré PB, Garzoni L, Bianchetti MG.

Pediatr Nephrol. 2012 May;27(5):733-9. doi: 10.1007/s00467-011-2093-5. Epub 2012 Jan 12. Review.

PMID:
22237777
18.

Conditions underlying significant community-acquired hyponatremia in childhood.

Bettinelli A, Aliprandi S, Bianchetti MG.

Acta Paediatr. 2011 Oct;100(10):e145-6. doi: 10.1111/j.1651-2227.2011.02421.x. Epub 2011 Aug 18. No abstract available.

PMID:
21767314
19.

Acute hemorrhagic edema of young children: a concise narrative review.

Fiore E, Rizzi M, Simonetti GD, Garzoni L, Bianchetti MG, Bettinelli A.

Eur J Pediatr. 2011 Dec;170(12):1507-11. doi: 10.1007/s00431-011-1508-4. Epub 2011 Jun 15. Review.

20.

Pregnancy in inherited hypokalemic salt-losing renal tubular disorder.

Mascetti L, Bettinelli A, Simonetti GD, Tagliabue A, Syrén ML, Nordio F, Bianchetti MG.

Obstet Gynecol. 2011 Feb;117(2 Pt 2):512-6. doi: 10.1097/AOG.0b013e3182075317.

PMID:
21252808
21.

Antimicrobial resistance among Escherichia coli that cause childhood community-acquired urinary tract infections in Northern Italy.

Caracciolo A, Bettinelli A, Bonato C, Isimbaldi C, Tagliabue A, Longoni L, Bianchetti MG.

Ital J Pediatr. 2011 Jan 6;37:3. doi: 10.1186/1824-7288-37-3.

22.

Body fluids and salt metabolism - part II.

Peruzzo M, Milani GP, Garzoni L, Longoni L, Simonetti GD, Bettinelli A, Fossali EF, Bianchetti MG.

Ital J Pediatr. 2010 Dec 13;36(1):78. doi: 10.1186/1824-7288-36-78. Review.

23.

The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestor.

Syrén ML, Borsa Ghiringhelli N, Bettinelli A, Colussi G, Vargas-Poussou R, Tammaro F, Coviello DA, Tedeschi S; Italian Collaborative Group for Gitelman Syndrome.

Nephrol Dial Transplant. 2011 Feb;26(2):557-61. doi: 10.1093/ndt/gfq458. Epub 2010 Jul 30.

PMID:
20675610
24.

Preference for formulations containing calcium and vitamin D(3) in childhood: a randomized-sequence, open-label trial.

Bianchetti AA, Lava SA, Bettinelli A, Rizzi M, Simonetti GD, Bianchetti MG.

Clin Ther. 2010 Jun;32(6):1083-7. doi: 10.1016/j.clinthera.2010.06.006.

PMID:
20637962
25.

Early appearance of hypokalemia in Gitelman syndrome.

Tammaro F, Bettinelli A, Cattarelli D, Cavazza A, Colombo C, Syrén ML, Tedeschi S, Bianchetti MG.

Pediatr Nephrol. 2010 Oct;25(10):2179-82. doi: 10.1007/s00467-010-1575-1. Epub 2010 Jun 16.

PMID:
20552229
26.

Cardiac arrhythmias and rhabdomyolysis in Bartter-Gitelman patients.

Cortesi C, Lava SA, Bettinelli A, Tammaro F, Giannini O, Caiata-Zufferey M, Bianchetti MG.

Pediatr Nephrol. 2010 Oct;25(10):2005-8. doi: 10.1007/s00467-010-1580-4. Epub 2010 Jun 13.

PMID:
20549246
27.

Long-term follow-up of patients with Bartter syndrome type I and II.

Puricelli E, Bettinelli A, Borsa N, Sironi F, Mattiello C, Tammaro F, Tedeschi S, Bianchetti MG; Italian Collaborative Group for Bartter Syndrome.

Nephrol Dial Transplant. 2010 Sep;25(9):2976-81. doi: 10.1093/ndt/gfq119. Epub 2010 Mar 10.

28.

Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature.

Pezzella M, Yeghiazaryan NS, Veggiotti P, Bettinelli A, Giudizioso G, Zara F, Striano P, Minetti C.

Seizure. 2010 Mar;19(2):132-5. doi: 10.1016/j.seizure.2009.12.002. Epub 2010 Jan 18. Review.

29.

Hypokalemic rhabdomyolysis in congenital tubular disorders: a case series and a systematic review.

von Vigier RO, Ortisi MT, La Manna A, Bianchetti MG, Bettinelli A.

Pediatr Nephrol. 2010 May;25(5):861-6. doi: 10.1007/s00467-009-1388-2. Epub 2009 Dec 22. Review.

PMID:
20033223
30.

Body fluids and salt metabolism - Part I.

Bianchetti MG, Simonetti GD, Bettinelli A.

Ital J Pediatr. 2009 Nov 19;35(1):36. doi: 10.1186/1824-7288-35-36.

31.

Vasculitides associated with IgG antineutrophil cytoplasmic autoantibodies in childhood.

Vanoni F, Bettinelli A, Keller F, Bianchetti MG, Simonetti GD.

Pediatr Nephrol. 2010 Feb;25(2):205-12. doi: 10.1007/s00467-009-1253-3. Epub 2009 Jul 30. Review.

32.

Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease.

Wu F, Reed AA, Williams SE, Loh NY, Lippiat JD, Christie PT, Large O, Bettinelli A, Dillon MJ, Goldraich NP, Hoppe B, Lhotta K, Loirat C, Malik R, Morel D, Kotanko P, Roussel B, Rubinger D, Schrander-Stumpel C, Serdaroglu E, Nesbit MA, Ashcroft F, Thakker RV.

Nephron Physiol. 2009;112(4):p53-62. doi: 10.1159/000225944. Epub 2009 Jun 20.

PMID:
19546591
33.

Body mass index modulates postural proteinuria.

Milani G, Bianchetti MG, Bozzani S, Bettinelli A, Fossali EF.

Int Urol Nephrol. 2010 Jun;42(2):513-5. doi: 10.1007/s11255-009-9550-0. Epub 2009 Mar 13. No abstract available.

PMID:
19283505
34.

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.

Clin J Am Soc Nephrol. 2007 May;2(3):454-60. Epub 2007 Mar 14.

35.

Monolateral visual loss due to sphenoid sinus mucocele: a rare complication of transsphenoidal surgery.

Lavezzi E, Fatti LM, Bucciarelli L, Bettinelli A, Scacchi M, Cavagnini F.

J Endocrinol Invest. 2006 Dec;29(11):1021-2. No abstract available.

PMID:
17259802
36.

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.

Am J Kidney Dis. 2007 Jan;49(1):91-8.

PMID:
17185149
37.

Prescription of drugs blocking the renin-angiotensin system in Italian children.

Bianchetti MG, Ammenti A, Avolio L, Bettinelli A, Bosio M, Fossali E, La Manna A, Maringhini S, Pela I, Ratsch IM, Viganò S, Ardissino G; Italkid Project; CHIld Project.

Pediatr Nephrol. 2007 Jan;22(1):144-8. Epub 2006 Nov 7.

PMID:
17089178
38.

Type IV Bartter syndrome: report of two new cases.

Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F.

Pediatr Nephrol. 2006 Jun;21(6):766-70. Epub 2006 Apr 1.

PMID:
16583241
39.

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.

Pediatr Res. 2005 Dec;58(6):1269-73.

PMID:
16306206
40.

Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies.

Cortesi C, Bettinelli A, Emma F, Fischbach M, Bertolani P, Bianchetti MG.

Nephrol Dial Transplant. 2005 Sep;20(9):1981-3. Epub 2005 Jun 28.

PMID:
15985518
41.

Hypokalemic rhabdomyolysis in a child with Bartter's syndrome.

Pela I, Materassi M, Seracini D, Lavoratti G, Bettinelli A.

Pediatr Nephrol. 2005 Aug;20(8):1189-91. Epub 2005 Jun 8.

PMID:
15942789
42.

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.

Pediatr Nephrol. 2004 Dec;19(12):1413-5.

PMID:
15338397
43.

Normomagnesemic Gitelman's syndrome?

Truttmann AC, Bettinelli A, Crosazzo L, Bianchetti MG.

Am J Kidney Dis. 2004 Jun;43(6):1143-4. No abstract available.

PMID:
15168407
44.

The Fanconi-Bickel syndrome: a case of neonatal onset.

Riva S, Ghisalberti C, Parini R, Furlan F, Bettinelli A, Somaschini M.

J Perinatol. 2004 May;24(5):322-3.

PMID:
15116130
45.

Normal plasma total magnesium in Gitelman syndrome.

Tosi F, Bianda ND, Truttmann AC, Crosazzo L, Bianchetti MG, Bettinelli A, Ramelli GP.

Am J Med. 2004 Apr 15;116(8):573-4. No abstract available.

PMID:
15063827
46.

Hypokalemia and hypomagnesemia of hereditary renal tubular origin. Bartter and Gitelman syndromes.

Bettinelli A, Tedeschi S.

Acta Biomed. 2003 Dec;74(3):163-7. English, Italian. No abstract available.

PMID:
15055023
47.

Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome).

Foglia PE, Bettinelli A, Tosetto C, Cortesi C, Crosazzo L, Edefonti A, Bianchetti MG.

Nephrol Dial Transplant. 2004 Jun;19(6):1398-402. Epub 2004 Mar 19.

PMID:
15034158
48.

Risk factors for poor renal prognosis in children with hemolytic uremic syndrome.

Gianviti A, Tozzi AE, De Petris L, Caprioli A, Ravà L, Edefonti A, Ardissino G, Montini G, Zacchello G, Ferretti A, Pecoraro C, De Palo T, Caringella A, Gaido M, Coppo R, Perfumo F, Miglietti N, Ratsche I, Penza R, Capasso G, Maringhini S, Li Volti S, Setzu C, Pennesi M, Bettinelli A, Peratoner L, Pela I, Salvaggio E, Lama G, Maffei S, Rizzoni G.

Pediatr Nephrol. 2003 Dec;18(12):1229-35. Epub 2003 Oct 31.

PMID:
14593522
49.

Prevention of cardiac arrhythmias in pediatric patients with normotensive-hypokalemic tubulopathy. Current attitude among European pediatricians.

Cortesi C, Foglia PE, Bettinelli A, Bianchetti MG.

Pediatr Nephrol. 2003 Aug;18(8):729-30. Review.

PMID:
12921106
50.

The biochemical diagnosis of Gitelman disease and the definition of "hypocalciuria".

Bianchetti MG, Edefonti A, Bettinelli A.

Pediatr Nephrol. 2003 May;18(5):409-11. Review. No abstract available.

PMID:
12793424

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