Chiumello G - Search Results

1

Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

Alberti L, Proverbio MC, Costagliola S, Romoli R, Boldrighini B, Vigone MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Alberti L, et al. Among authors: chiumello g. J Clin Endocrinol Metab. 2002 Jun;87(6):2549-55. doi: 10.1210/jcem.87.6.8536. J Clin Endocrinol Metab. 2002. PMID: 12050212

2

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. Zamproni I, et al. Among authors: chiumello g. J Clin Endocrinol Metab. 2008 Feb;93(2):605-10. doi: 10.1210/jc.2007-2020. Epub 2007 Nov 27. J Clin Endocrinol Metab. 2008. PMID: 18042646 Free PMC article.

3

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. Corbetta C, et al. Among authors: chiumello g. Clin Endocrinol (Oxf). 2009 Nov;71(5):739-45. doi: 10.1111/j.1365-2265.2009.03568.x. Epub 2009 Mar 28. Clin Endocrinol (Oxf). 2009. PMID: 19486019

4

Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene.

Bonomi M, Proverbio MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Bonomi M, et al. Among authors: chiumello g. J Clin Endocrinol Metab. 2001 Apr;86(4):1600-4. doi: 10.1210/jcem.86.4.7411. J Clin Endocrinol Metab. 2001. PMID: 11297590

5

A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism.

Alberti L, Proverbio MC, Costagliola S, Weber G, Beck-Peccoz P, Chiumello G, Persani L. Alberti L, et al. Among authors: chiumello g. Eur J Endocrinol. 2001 Sep;145(3):249-54. doi: 10.1530/eje.0.1450249. Eur J Endocrinol. 2001. PMID: 11517004

6

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. Vigone MC, et al. Among authors: chiumello g. J Pediatr Endocrinol Metab. 2012;25(1-2):153-5. doi: 10.1515/jpem.2011.438. J Pediatr Endocrinol Metab. 2012. PMID: 22570966

7

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. Rabbiosi S, et al. Among authors: chiumello g. J Clin Endocrinol Metab. 2013 Apr;98(4):1395-402. doi: 10.1210/jc.2012-3174. Epub 2013 Feb 20. J Clin Endocrinol Metab. 2013. PMID: 23426615 Free article.

8

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. Vigone MC, et al. Among authors: chiumello g. Hum Mutat. 2005 Oct;26(4):395. doi: 10.1002/humu.9372. Hum Mutat. 2005. PMID: 16134168

9

Measurement of urinary iodine excretion to reveal iodine excess in neonatal transient hypothyroidism.

Bona G, Chiorboli E, Rapa A, Weber G, Vigone MC, Chiumello G. Bona G, et al. Among authors: chiumello g. J Pediatr Endocrinol Metab. 1998 Nov-Dec;11(6):739-43. doi: 10.1515/jpem.1998.11.6.739. J Pediatr Endocrinol Metab. 1998. PMID: 9829229

10

Congenital hypothyroidism with gland in situ: diagnostic re-evaluation.

Weber G, Vigone MC, Passoni A, Odoni M, Paesano PL, Dosio F, Proverbio MC, Corbetta C, Persani L, Chiumello G. Weber G, et al. Among authors: chiumello g. J Endocrinol Invest. 2005 Jun;28(6):516-22. doi: 10.1007/BF03347239. J Endocrinol Invest. 2005. PMID: 16117192

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