Melis D - Search Results

1

Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype.

Genesio R, Melis D, Gatto S, Izzo A, Ronga V, Cappuccio G, Lanzo A, Andria G, D'Esposito M, Matarazzo MR, Conti A, Nitsch L. Genesio R, et al. Among authors: d esposito m, melis d. Epigenetics. 2011 Oct 1;6(10):1242-7. doi: 10.4161/epi.6.10.17698. Epub 2011 Oct 1. Epigenetics. 2011. PMID: 21931280 Free article.

2

Should patients perception of health status be integrated in the prognostic assessment of heart failure patients? A prospective study.

Network of Nurses of GISSI-HF; Di Giulio P. Network of Nurses of GISSI-HF, et al. Qual Life Res. 2014 Feb;23(1):49-56. doi: 10.1007/s11136-013-0468-8. Epub 2013 Aug 4. Qual Life Res. 2014. PMID: 23912852 Free article. Clinical Trial.

3

Mild phenotype associated with an interstitial deletion of the long arm of chromosome 1.

Melis D, Perone L, Sperandeo MP, Sabbatino MS, Tuzzi MR, Romano A, Parenti G, Andria G. Melis D, et al. J Med Genet. 1998 Dec;35(12):1047-9. doi: 10.1136/jmg.35.12.1047. J Med Genet. 1998. PMID: 9863608 Free PMC article.

4

Crohn's-like ileo-colitis in patients affected by glycogen storage disease Ib: two years' follow-up of patients with a wide spectrum of gastrointestinal signs.

Melis D, Parenti G, Della Casa R, Sibilio M, Berni Canani R, Terrin G, Cucchiara S, Andria G. Melis D, et al. Acta Paediatr. 2003 Dec;92(12):1415-21. doi: 10.1080/08035250310007033. Acta Paediatr. 2003. PMID: 14971792

5

Brain damage in glycogen storage disease type I.

Melis D, Parenti G, Della Casa R, Sibilio M, Romano A, Di Salle F, Elefante R, Mansi G, Santoro L, Perretti A, Paludetto R, Sequino L, Andria G. Melis D, et al. J Pediatr. 2004 May;144(5):637-42. doi: 10.1016/j.jpeds.2004.02.033. J Pediatr. 2004. PMID: 15127000

6

A new familial case of spondylo-epi-metaphyseal dysplasia with multiple dislocations Hall type (leptodactylic form).

Rossi M, De Brasi D, Hall CM, Battagliese A, Melis D, Sebastio G, Andria G. Rossi M, et al. Among authors: melis d. Clin Dysmorphol. 2005 Jan;14(1):13-18. Clin Dysmorphol. 2005. PMID: 15602087

7

Genotype/phenotype correlation in glycogen storage disease type 1b: a multicentre study and review of the literature.

Melis D, Fulceri R, Parenti G, Marcolongo P, Gatti R, Parini R, Riva E, Della Casa R, Zammarchi E, Andria G, Benedetti A. Melis D, et al. Eur J Pediatr. 2005 Aug;164(8):501-8. doi: 10.1007/s00431-005-1657-4. Epub 2005 May 19. Eur J Pediatr. 2005. PMID: 15906092 Review.

8

Mosaic 13q13.2-ter deletion restricted to tissues of ectodermal and mesodermal origins.

Melis D, Pia Sperandeo M, Perone L, Staiano A, Andria G, Sebastio G. Melis D, et al. Clin Dysmorphol. 2006 Jan;15(1):13-18. doi: 10.1097/01.mcd.0000181602.70629.67. Clin Dysmorphol. 2006. PMID: 16317301

9

Increased prevalence of thyroid autoimmunity and hypothyroidism in patients with glycogen storage disease type I.

Melis D, Pivonello R, Parenti G, Della Casa R, Salerno M, Lombardi G, Sebastio G, Colao A, Andria G. Melis D, et al. J Pediatr. 2007 Mar;150(3):300-5, 305.e1. doi: 10.1016/j.jpeds.2006.11.056. J Pediatr. 2007. PMID: 17307551

10

Trisomy 18 and hypertrophy cardiomyopathy in an 18-year-old woman.

Limongelli G, Pacileo G, Melis D, Calabro' P, Digilio MC, Sarkozy A, Maddaloni V, Capozzi G, Sebastio G, Andria G, Calabro' R. Limongelli G, et al. Among authors: melis d. Am J Med Genet A. 2008 Feb 1;146A(3):327-9. doi: 10.1002/ajmg.a.32149. Am J Med Genet A. 2008. PMID: 18203191 No abstract available.

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