Milana G - Search Results

1

No association between apolipoprotein E polymorphisms and recurrent pregnancy loss.

Bianca S, Barrano B, Cutuli N, Indaco L, Cataliotti A, Milana G, Barone C, Ettore G. Bianca S, et al. Among authors: milana g. Fertil Steril. 2010 Jan;93(1):276. doi: 10.1016/j.fertnstert.2009.07.971. Epub 2009 Sep 3. Fertil Steril. 2010. PMID: 19732892 Free article.

2

Recurrent pregnancy loss and inherited thrombophilia: who should be tested?

Bianca S, Barrano B, Cutuli N, Indaco L, Ingegnosi C, Cataliotti A, Milana G, Ettore G. Bianca S, et al. Among authors: milana g. J Clin Pathol. 2008 Oct;61(10):1149-50. doi: 10.1136/jcp.2008.060525. J Clin Pathol. 2008. PMID: 18820106 No abstract available.

3

Unexplained infertility and inherited thrombophilia.

Bianca S, Barrano B, Cutuli N, Indaco L, Cataliotti A, Milana G, Barone C, Ettore G. Bianca S, et al. Among authors: milana g. Fertil Steril. 2009 Jul;92(1):e4; author reply e5. doi: 10.1016/j.fertnstert.2009.02.007. Epub 2009 May 23. Fertil Steril. 2009. PMID: 19476939 Free article. No abstract available.

4

Hereditary haemorrhagic telangiectasia and genetic thrombophilia.

Bianca S, Cutuli N, Bianca M, Barrano B, Cataliotti A, Barone C, Indaco L, Milana G. Bianca S, et al. Among authors: milana g. Eur J Hum Genet. 2010 Apr;18(4):405; author reply 405-6. doi: 10.1038/ejhg.2009.204. Epub 2009 Nov 11. Eur J Hum Genet. 2010. PMID: 19904300 Free PMC article. No abstract available.

5

Clinical management of Rendu-Osler-Weber syndrome and genetic thrombophilia.

Bianca S, Cutuli N, Bianca M, Barrano B, Cataliotti A, Barone C, Milana G. Bianca S, et al. Among authors: milana g. Blood Coagul Fibrinolysis. 2009 Dec;20(8):733. doi: 10.1097/MBC.0b013e32832f42e8. Blood Coagul Fibrinolysis. 2009. PMID: 20519971 Clinical Trial. No abstract available.

6

High prevalence of hepatitis G virus in multitransfused Sicilian patients with beta-thalassaemia.

Cutuli N, Milana G, Musumeci S. Cutuli N, et al. Among authors: milana g. Vox Sang. 2000;79(4):247. doi: 10.1159/000056740. Vox Sang. 2000. PMID: 11155079 No abstract available.

7

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G. Gangarossa S, et al. Among authors: milana g. Am J Med Genet. 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882392

8

Routine clinical application of the FRAXA Pfu PCR assay: limits and utility.

Condorelli DF, Milana G, Dell'Albani P, Roccazzello AM, Insirello E, Pavone L, Mollica F. Condorelli DF, et al. Among authors: milana g. Clin Genet. 1996 Nov;50(5):366-71. doi: 10.1111/j.1399-0004.1996.tb02389.x. Clin Genet. 1996. PMID: 9007325

9

Unstable translocations: a new case?

Mattina T, Milana G, D'Agata A, Conti L, Sciacca F. Mattina T, et al. Among authors: milana g. Clin Genet. 1991 Feb;39(2):149-50. doi: 10.1111/j.1399-0004.1991.tb03002.x. Clin Genet. 1991. PMID: 1826645

10

Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities.

Dunnill MG, Richards AJ, Milana G, Mollica F, Atherton D, Winship I, Farrall M, al-Imara L, Eady RA, Pope FM. Dunnill MG, et al. Among authors: milana g. J Med Genet. 1994 Oct;31(10):745-8. doi: 10.1136/jmg.31.10.745. J Med Genet. 1994. PMID: 7837248 Free PMC article.

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