Cirillo G - Search Results

1

Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis.

Grandone A, Torella A, Santoro C, Giugliano T, Del Vecchio Blanco F, Mutarelli M, Cirillo M, Cirillo G, Piluso G, Capristo C, Festa A, Marzuillo P, Miraglia Del Giudice E, Perrone L, Nigro V. Grandone A, et al. Among authors: cirillo g, cirillo m. Clin Genet. 2016 Nov;90(5):445-450. doi: 10.1111/cge.12771. Epub 2016 Apr 29. Clin Genet. 2016. PMID: 26940245

2

Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor.

Miraglia del Giudice E, Coppola G, Scuccimarra G, Cirillo G, Bellini G, Pascotto A. Miraglia del Giudice E, et al. Among authors: cirillo g. Eur J Hum Genet. 2000 Dec;8(12):994-7. doi: 10.1038/sj.ejhg.5200570. Eur J Hum Genet. 2000. PMID: 11175290

3

Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations.

Miraglia del Giudice E, Cirillo G, Santoro N, D'Urso L, Carbone MT, Di Toro R, Perrone L. Miraglia del Giudice E, et al. Among authors: cirillo g. Int J Obes Relat Metab Disord. 2001 Jan;25(1):61-7. doi: 10.1038/sj.ijo.0801485. Int J Obes Relat Metab Disord. 2001. PMID: 11244459

4

Mutational screening of the CART gene in obese children: identifying a mutation (Leu34Phe) associated with reduced resting energy expenditure and cosegregating with obesity phenotype in a large family.

del Giudice EM, Santoro N, Cirillo G, D'Urso L, Di Toro R, Perrone L. del Giudice EM, et al. Among authors: cirillo g. Diabetes. 2001 Sep;50(9):2157-60. doi: 10.2337/diabetes.50.9.2157. Diabetes. 2001. PMID: 11522684

5

Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity.

Miraglia Del Giudice E, Cirillo G, Nigro V, Santoro N, D'Urso L, Raimondo P, Cozzolino D, Scafato D, Perrone L. Miraglia Del Giudice E, et al. Among authors: cirillo g. Int J Obes Relat Metab Disord. 2002 May;26(5):647-51. doi: 10.1038/sj.ijo.0801983. Int J Obes Relat Metab Disord. 2002. PMID: 12032748

6

Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity.

Miraglia del Giudice E, Santoro N, Cirillo G, Raimondo P, Grandone A, D'Aniello A, Di Nardo M, Perrone L. Miraglia del Giudice E, et al. Among authors: cirillo g. Int J Obes Relat Metab Disord. 2004 Mar;28(3):447-50. doi: 10.1038/sj.ijo.0802572. Int J Obes Relat Metab Disord. 2004. PMID: 14724664

7

An insertional polymorphism of the proopiomelanocortin gene is associated with fasting insulin levels in childhood obesity.

Santoro N, del Giudice EM, Cirillo G, Raimondo P, Corsi I, Amato A, Grandone A, Perrone L. Santoro N, et al. Among authors: cirillo g. J Clin Endocrinol Metab. 2004 Oct;89(10):4846-9. doi: 10.1210/jc.2004-0333. J Clin Endocrinol Metab. 2004. PMID: 15472174

8

Melanocortin-4 receptor molecular scanning and pro-opiomelanocortin R236G variant screening in binge eating disorder.

Tortorella A, Monteleone P, del Giudice EM, Cirillo G, Perrone L, Castaldo E, Maj M. Tortorella A, et al. Among authors: cirillo g. Psychiatr Genet. 2005 Sep;15(3):161. doi: 10.1097/00041444-200509000-00004. Psychiatr Genet. 2005. PMID: 16094248 No abstract available.

9

Weight loss in obese children carrying the proopiomelanocortin R236G variant.

Santoro N, Perrone L, Cirillo G, Raimondo P, Amato A, Coppola F, Santarpia M, D'Aniello A, Miraglia Del Giudice E. Santoro N, et al. Among authors: cirillo g. J Endocrinol Invest. 2006 Mar;29(3):226-30. doi: 10.1007/BF03345544. J Endocrinol Invest. 2006. PMID: 16682835

10

Insulin gene variable number of tandem repeats (INS VNTR) genotype and metabolic syndrome in childhood obesity.

Santoro N, Cirillo G, Amato A, Luongo C, Raimondo P, D'Aniello A, Perrone L, Miraglia del Giudice E. Santoro N, et al. Among authors: cirillo g. J Clin Endocrinol Metab. 2006 Nov;91(11):4641-4. doi: 10.1210/jc.2005-2705. Epub 2006 Jul 25. J Clin Endocrinol Metab. 2006. PMID: 16868061

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