Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 304

1.

Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study.

Fintini D, Grugni G, Bocchini S, Brufani C, Di Candia S, Corrias A, Delvecchio M, Salvatoni A, Ragusa L, Greggio N, Franzese A, Scarano E, Trifirò G, Mazzanti L, Chiumello G, Cappa M, Crinò A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

Nutr Metab Cardiovasc Dis. 2016 Sep;26(9):842-7. doi: 10.1016/j.numecd.2016.05.010. Epub 2016 Jun 3.

PMID:
27381990
2.

Necrobiosis Lipoidica Diabeticorum: A pediatric case report.

Bonura C, Frontino G, Rigamonti A, Battaglino R, Favalli V, Ferro G, Rubino C, Del Barba P, Pesapane F, Nazzaro G, Gianotti R, Bonfanti R, Meschi F, Chiumello G.

Dermatoendocrinol. 2014 Jan 1;6(1):e27790. doi: 10.4161/derm.27790. Epub 2014 Jan 17.

3.

Severe hypoglycemia and ketoacidosis over one year in Italian pediatric population with type 1 diabetes mellitus: a multicenter retrospective observational study.

Cherubini V, Pintaudi B, Rossi MC, Lucisano G, Pellegrini F, Chiumello G, Frongia AP, Monciotti C, Patera IP, Toni S, Zucchini S, Nicolucci A; SHIP-D Study Group.

Nutr Metab Cardiovasc Dis. 2014 May;24(5):538-46. doi: 10.1016/j.numecd.2013.11.004. Epub 2013 Dec 3.

PMID:
24418381
4.

Sexual function in adult life following Passerini-Glazel feminizing genitoplasty in patients with congenital adrenal hyperplasia.

Lesma A, Bocciardi A, Corti S, Chiumello G, Rigatti P, Montorsi F.

J Urol. 2014 Jan;191(1):206-11. doi: 10.1016/j.juro.2013.07.097. Epub 2013 Aug 6.

PMID:
23933397
5.

Growth hormone therapy and respiratory disorders: long-term follow-up in PWS children.

Berini J, Spica Russotto V, Castelnuovo P, Di Candia S, Gargantini L, Grugni G, Iughetti L, Nespoli L, Nosetti L, Padoan G, Pilotta A, Trifirò G, Chiumello G, Salvatoni A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

J Clin Endocrinol Metab. 2013 Sep;98(9):E1516-23. doi: 10.1210/jc.2013-1831. Epub 2013 Jul 26.

PMID:
23894156
6.

Rare cases of autoimmune hypothyroidism in young children.

Tronconi GM, Caiulo S, Di Frenna M, Vigone MC, Chiumello G, Weber G.

J Pediatr Endocrinol Metab. 2013;26(9-10):963-6. doi: 10.1515/jpem-2012-0423.

PMID:
23612641
7.

Future Perspectives in Glucose Monitoring Sensors.

Frontino G, Meschi F, Bonfanti R, Rigamonti A, Battaglino R, Favalli V, Bonura C, Ferro G, Chiumello G.

Eur Endocrinol. 2013 Mar;9(1):6-11. doi: 10.17925/EE.2013.09.01.21. Epub 2013 Mar 15. Review.

8.

Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation.

Rabbiosi S, Vigone MC, Cortinovis F, Zamproni I, Fugazzola L, Persani L, Corbetta C, Chiumello G, Weber G.

J Clin Endocrinol Metab. 2013 Apr;98(4):1395-402. doi: 10.1210/jc.2012-3174. Epub 2013 Feb 20.

9.

Central adrenal insufficiency in young adults with Prader-Willi syndrome.

Grugni G, Beccaria L, Corrias A, Crinò A, Cappa M, De Medici C, Di Candia S, Gargantini L, Ragusa L, Salvatoni A, Sartorio A, Spera S, Andrulli S, Chiumello G, Mussa A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

Clin Endocrinol (Oxf). 2013 Sep;79(3):371-8. doi: 10.1111/cen.12150. Epub 2013 May 11.

PMID:
23311724
10.

Metabolic syndrome in adult patients with Prader-Willi syndrome.

Grugni G, Crinò A, Bedogni G, Cappa M, Sartorio A, Corrias A, Di Candia S, Gargantini L, Iughetti L, Pagano C, Ragusa L, Salvatoni A, Spera S, Vettor R, Chiumello G, Brambilla P.

Nutr Metab Cardiovasc Dis. 2013 Nov;23(11):1134-40. doi: 10.1016/j.numecd.2012.11.006. Epub 2012 Dec 7.

PMID:
23220075
11.

POI: a score to modulate GH treatment in children with Prader-Willi syndrome.

Salvatoni A, Berini J, Chiumello G, Crinò A, Di Candia S, Gargantini L, Grugni G, Iughetti L, Luce A, Musolino G, Sogno Valin P, Spica Russotto V, Trifirò G.

Horm Res Paediatr. 2012;78(3):201-2. doi: 10.1159/000342649. Epub 2012 Sep 11. No abstract available.

PMID:
22986481
12.

[Long term efficacy of insulin pump therapy in preschool children with diabetes].

Favalli V, Bonfanti R, Meschi F, Viscardi M, Rigamonti A, Biffi V, Frontino G, Battaglino R, Bonura C, Chiumello G.

Pediatr Med Chir. 2012 May-Jun;34(3):129-32. Italian. No abstract available.

PMID:
22966725
13.

Asymptomatic thyrotropin-secreting pituitary macroadenoma in a 13-year-old girl: successful first-line treatment with somatostatin analogs.

Rabbiosi S, Peroni E, Tronconi GM, Chiumello G, Losa M, Weber G.

Thyroid. 2012 Oct;22(10):1076-9. doi: 10.1089/thy.2012.0077. Epub 2012 Sep 4.

PMID:
22947349
14.

Sensor-augmented pump therapy in very young children with type 1 diabetes: an efficacy and feasibility observational study.

Frontino G, Bonfanti R, Scaramuzza A, Rabbone I, Meschi F, Rigamonti A, Battaglino R, Favalli V, Bonura C, Sicignano S, Gioia E, Zuccotti GV, Cerutti F, Chiumello G.

Diabetes Technol Ther. 2012 Sep;14(9):762-4. doi: 10.1089/dia.2012.0044. Epub 2012 Jun 13.

PMID:
22694194
15.

46,XY karyotype in a female phenotype fetus: a challenging diagnosis.

Russo G, di Lascio A, Ferrario M, Meroni S, Hiort O, Chiumello G.

J Pediatr Adolesc Gynecol. 2012 Jun;25(3):e77-9. doi: 10.1016/j.jpag.2012.03.001.

PMID:
22578489
16.

Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangioma.

Vigone MC, Cortinovis F, Rabbiosi S, Di Frenna M, Passoni A, Persani L, Chiumello G, Gelmetti C, Weber G.

J Pediatr Endocrinol Metab. 2012;25(1-2):153-5.

PMID:
22570966
17.

Surgical management of pediatric Graves' disease: an effective definitive treatment.

Peroni E, Angiolini MR, Vigone MC, Mari G, Chiumello G, Beretta E, Weber G.

Pediatr Surg Int. 2012 Jun;28(6):609-14. doi: 10.1007/s00383-012-3095-5. Epub 2012 Apr 29.

PMID:
22543510
18.

[Glucose monitoring in children with type 1 diabetes mellitus. New insights].

Battaglino R, Bonfanti R, Favalli V, Viscardi M, Meschi F, Chiumello G.

Pediatr Med Chir. 2011 Sep-Dec;33(5-6):217-20. Italian. No abstract available.

PMID:
22428429
19.

GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.

Ludvigsson J, Krisky D, Casas R, Battelino T, Castaño L, Greening J, Kordonouri O, Otonkoski T, Pozzilli P, Robert JJ, Veeze HJ, Palmer J, Samuelsson U, Elding Larsson H, Åman J, Kärdell G, Neiderud Helsingborg J, Lundström G, Albinsson E, Carlsson A, Nordvall M, Fors H, Arvidsson CG, Edvardson S, Hanås R, Larsson K, Rathsman B, Forsgren H, Desaix H, Forsander G, Nilsson NÖ, Åkesson CG, Keskinen P, Veijola R, Talvitie T, Raile K, Kapellen T, Burger W, Neu A, Engelsberger I, Heidtmann B, Bechtold S, Leslie D, Chiarelli F, Cicognani A, Chiumello G, Cerutti F, Zuccotti GV, Gomez Gila A, Rica I, Barrio R, Clemente M, López Garcia MJ, Rodriguez M, Gonzalez I, Lopez JP, Oyarzabal M, Reeser HM, Nuboer R, Stouthart P, Bratina N, Bratanic N, de Kerdanet M, Weill J, Ser N, Barat P, Bertrand AM, Carel JC, Reynaud R, Coutant R, Baron S.

N Engl J Med. 2012 Feb 2;366(5):433-42. doi: 10.1056/NEJMoa1107096.

20.

Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome.

Corrias A, Grugni G, Crinò A, Di Candia S, Chiabotto P, Cogliardi A, Chiumello G, De Medici C, Spera S, Gargantini L, Iughetti L, Luce A, Mariani B, Ragusa L, Salvatoni A, Andrulli S, Mussa A, Beccaria L; Study Group for Genetic Obesity of Italian Society of Pediatric Endocrinology and Diabetology (SIEDP/ISPED).

Clin Endocrinol (Oxf). 2012 Jun;76(6):843-50. doi: 10.1111/j.1365-2265.2011.04313.x.

PMID:
22150958
21.

Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports.

Donghi V, Di Frenna M, di Lascio A, Chiumello G, Weber G.

J Pediatr Endocrinol Metab. 2011;24(9-10):801-5.

PMID:
22145480
22.

Early onset of puberty in young girls: an Italian cross-sectional study.

Russo G, Brambilla P, Della Beffa F, Ferrario M, Pitea M, Mastropietro T, Marinello R, Picca M, Nizzoli G, Chiumello G.

J Endocrinol Invest. 2012 Oct;35(9):804-8. doi: 10.3275/8062. Epub 2011 Nov 8.

PMID:
22082715
23.

Neurosurgical treatment of craniopharyngioma in adults and children: early and long-term results in a large case series.

Mortini P, Losa M, Pozzobon G, Barzaghi R, Riva M, Acerno S, Angius D, Weber G, Chiumello G, Giovanelli M.

J Neurosurg. 2011 May;114(5):1350-9. doi: 10.3171/2010.11.JNS10670. Epub 2011 Jan 7.

PMID:
21214336
24.

Patients' evaluation of nocturnal hypoglycaemia with GlucoDay continuous glucose monitoring in paediatric patients.

Meschi F, Bonfanti R, Rigamonti A, Giulio F, Battaglino R, Viscardi M, Poscia A, Chiumello G.

Acta Diabetol. 2010 Dec;47(4):295-300. doi: 10.1007/s00592-010-0181-9. Epub 2010 Mar 27.

PMID:
20683627
25.

Newborn of mothers affected by autoimmune thyroiditis: the importance of thyroid function monitoring in the first months of life.

Rovelli R, Vigone MC, Giovanettoni C, Passoni A, Maina L, Corrias A, Corbetta C, Mosca F, Chiumello G, Weber G.

Ital J Pediatr. 2010 Mar 10;36:24. doi: 10.1186/1824-7288-36-24.

26.

Pediatric otorhinolaryngologic manifestations of endocrinological pathologies.

Luce FL, Sarandria D, Pozzobon G, Chiumello G, Bussi M.

Int J Pediatr Otorhinolaryngol. 2009 Dec;73 Suppl 1:S49-55. doi: 10.1016/S0165-5876(09)70010-2. Review.

PMID:
20114156
27.

Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesity.

Brambilla P, Crinò A, Bedogni G, Bosio L, Cappa M, Corrias A, Delvecchio M, Di Candia S, Gargantini L, Grechi E, Iughetti L, Mussa A, Ragusa L, Sacco M, Salvatoni A, Chiumello G, Grugni G; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

Nutr Metab Cardiovasc Dis. 2011 Apr;21(4):269-76. doi: 10.1016/j.numecd.2009.10.004. Epub 2010 Jan 20.

PMID:
20089384
28.

A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs.

Crinò A, Di Giorgio G, Livieri C, Grugni G, Beccaria L, Bosio L, Corrias A, Chiumello G, Trifirò G, Salvatoni A, Tonini G, Gargantini L, de Toni T, Valerio G, Ragusa L, Franzese A, Rinaldi MM, Spera S, Gattinara GC, Villani S, Iughetti L; Genetic Obesity Study Group; Italian Society of Pediatric Endocrinology and Diabetology.

J Pediatr Endocrinol Metab. 2009 Oct;22(10):883-93.

PMID:
20020576
29.

Pseudohypoparathyroidism, an often delayed diagnosis: a case series.

Donghi V, Mora S, Zamproni I, Chiumello G, Weber G.

Cases J. 2009 May 28;2:6734. doi: 10.1186/1757-1626-2-6734.

30.

Short-term effects of growth hormone treatment on the upper airways of non severely obese children with Prader-Willi syndrome.

Salvatoni A, Veronelli E, Nosetti L, Berini J, de Simone S, Iughetti L, Bosio L, Chiumello G, Grugni G, Delù G, Castelnuovo P, Trifirò G, Nespoli L.

J Endocrinol Invest. 2009 Jul;32(7):601-5. doi: 10.3275/6295. Epub 2009 May 15.

PMID:
19498323
31.

17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.

Bertelloni S, Balsamo A, Giordani L, Fischetto R, Russo G, Delvecchio M, Gennari M, Nicoletti A, Maggio MC, Concolino D, Cavallo L, Cicognani A, Chiumello G, Hiort O, Baroncelli GI, Faienza MF.

J Endocrinol Invest. 2009 Sep;32(8):666-70. doi: 10.3275/6281. Epub 2009 May 12.

PMID:
19498320
32.

A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH).

Corbetta C, Weber G, Cortinovis F, Calebiro D, Passoni A, Vigone MC, Beck-Peccoz P, Chiumello G, Persani L.

Clin Endocrinol (Oxf). 2009 Nov;71(5):739-45. doi: 10.1111/j.1365-2265.2009.03568.x. Epub 2009 Mar 28.

PMID:
19486019
33.

Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene.

Di Candia S, Gessi A, Pepe G, Sogno Valin P, Mangano E, Chiumello G, Gianolli L, Proverbio MC, Mora S.

Eur J Endocrinol. 2009 Jun;160(6):1019-23. doi: 10.1530/EJE-08-0945. Epub 2009 Mar 24.

PMID:
19318379
34.

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

Gambineri E, Perroni L, Passerini L, Bianchi L, Doglioni C, Meschi F, Bonfanti R, Sznajer Y, Tommasini A, Lawitschka A, Junker A, Dunstheimer D, Heidemann PH, Cazzola G, Cipolli M, Friedrich W, Janic D, Azzi N, Richmond E, Vignola S, Barabino A, Chiumello G, Azzari C, Roncarolo MG, Bacchetta R.

J Allergy Clin Immunol. 2008 Dec;122(6):1105-1112.e1. doi: 10.1016/j.jaci.2008.09.027. Epub 2008 Oct 25.

PMID:
18951619
35.

Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies.

Bonfanti R, Colombo C, Nocerino V, Massa O, Lampasona V, Iafusco D, Viscardi M, Chiumello G, Meschi F, Barbetti F.

Diabetes Care. 2009 Jan;32(1):123-5. doi: 10.2337/dc08-0783. Epub 2008 Oct 7.

36.

Estrogen exposure in a child from hair lotion used by her mother: clinical and hair analysis data.

Guarneri MP, Brambilla G, Loizzo A, Colombo I, Chiumello G.

Clin Toxicol (Phila). 2008 Sep;46(8):762-4. doi: 10.1080/15563650701638941.

PMID:
18763154
37.

Decreased parietal cortex activity during mental rotation in children with congenital hypothyroidism.

Blasi V, Longaretti R, Giovanettoni C, Baldoli C, Pontesilli S, Vigone C, Saccuman C, Nigro F, Chiumello G, Scotti G, Weber G.

Neuroendocrinology. 2009;89(1):56-65. doi: 10.1159/000151397. Epub 2008 Aug 13.

PMID:
18698134
38.

The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.

Grugni G, Crinò A, Bosio L, Corrias A, Cuttini M, De Toni T, Di Battista E, Franzese A, Gargantini L, Greggio N, Iughetti L, Livieri C, Naselli A, Pagano C, Pozzan G, Ragusa L, Salvatoni A, Trifirò G, Beccaria L, Bellizzi M, Bellone J, Brunani A, Cappa M, Caselli G, Cerioni V, Delvecchio M, Giardino D, Iannì F, Memo L, Pilotta A, Pomara C, Radetti G, Sacco M, Sanzari A, Sartorio A, Tonini G, Vettor R, Zaglia F, Chiumello G; Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

Am J Med Genet A. 2008 Apr 1;146A(7):861-72. doi: 10.1002/ajmg.a.32133.

PMID:
18203198
39.

Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.

Zamproni I, Grasberger H, Cortinovis F, Vigone MC, Chiumello G, Mora S, Onigata K, Fugazzola L, Refetoff S, Persani L, Weber G.

J Clin Endocrinol Metab. 2008 Feb;93(2):605-10. Epub 2007 Nov 27.

40.

[Hyperinsuline hypoglycemias].

Chiumello G, Bosio L, Di Candia S, Sogno Valin P.

Minerva Pediatr. 2007 Oct;59(5):547. Italian. No abstract available.

PMID:
17947913
41.

Evidence for in vivo primed and expanded autoreactive T cells as a specific feature of patients with type 1 diabetes.

Monti P, Scirpoli M, Rigamonti A, Mayr A, Jaeger A, Bonfanti R, Chiumello G, Ziegler AG, Bonifacio E.

J Immunol. 2007 Nov 1;179(9):5785-92.

42.

Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy.

Biagiotti L, Proverbio MC, Bosio L, Gervasi F, Rovida E, Cerioni V, Bove M, Valin PS, Albarello L, Zamproni I, Grassi S, Doglioni C, Mora S, Chiumello G, Biunno I.

Exp Mol Pathol. 2007 Aug;83(1):59-64. Epub 2007 Jan 17.

PMID:
17316607
43.

[Endocrine disrupters and male gonads].

Guarneri MP, Colombo I, Chiumello G.

Minerva Pediatr. 2006 Aug;58(4):341-5. Review. Italian. No abstract available.

PMID:
17008842
44.

Persistent renal hypertrophy and faster decline of glomerular filtration rate precede the development of microalbuminuria in type 1 diabetes.

Zerbini G, Bonfanti R, Meschi F, Bognetti E, Paesano PL, Gianolli L, Querques M, Maestroni A, Calori G, Del Maschio A, Fazio F, Luzi L, Chiumello G.

Diabetes. 2006 Sep;55(9):2620-5.

45.

Reduced bone mineral density and increased bone metabolism rate in young adult patients with 21-hydroxylase deficiency.

Sciannamblo M, Russo G, Cuccato D, Chiumello G, Mora S.

J Clin Endocrinol Metab. 2006 Nov;91(11):4453-8. Epub 2006 Aug 22.

PMID:
16926248
46.

Insulin therapy and carbohydrate counting.

Chiesa G, Piscopo MA, Rigamonti A, Azzinari A, Bettini S, Bonfanti R, Viscardi M, Meschi F, Chiumello G.

Acta Biomed. 2005;76 Suppl 3:44-8.

PMID:
16915796
47.

Insulin resistance and whole body energy homeostasis in obese adolescents with fatty liver disease.

Perseghin G, Bonfanti R, Magni S, Lattuada G, De Cobelli F, Canu T, Esposito A, Scifo P, Ntali G, Costantino F, Bosio L, Ragogna F, Del Maschio A, Chiumello G, Luzi L.

Am J Physiol Endocrinol Metab. 2006 Oct;291(4):E697-703. Epub 2006 May 9.

48.

Adult height in patients with permanent growth hormone deficiency with and without multiple pituitary hormone deficiencies.

Maghnie M, Ambrosini L, Cappa M, Pozzobon G, Ghizzoni L, Ubertini MG, di Iorgi N, Tinelli C, Pilia S, Chiumello G, Lorini R, Loche S.

J Clin Endocrinol Metab. 2006 Aug;91(8):2900-5. Epub 2006 May 9.

PMID:
16684828
49.

Severe hypocalcemia due to a de novo mutation in the fifth transmembrane domain of the calcium-sensing receptor.

Mora S, Zamproni I, Proverbio MC, Bozzetti V, Chiumello G, Weber G.

Am J Med Genet A. 2006 Jan 1;140(1):98-101. No abstract available.

PMID:
16333828
50.

Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings.

Vigone MC, Fugazzola L, Zamproni I, Passoni A, Di Candia S, Chiumello G, Persani L, Weber G.

Hum Mutat. 2005 Oct;26(4):395.

PMID:
16134168

Supplemental Content

Loading ...
Support Center