Bicocchi MP - Search Results

1

Molecular cytogenetic definition of a translocation t(X;15) associated with premature ovarian failure.

Bertini V, Ghirri P, Bicocchi MP, Simi P, Valetto A. Bertini V, et al. Among authors: bicocchi mp. Fertil Steril. 2010 Aug;94(3):1097.e5-8. doi: 10.1016/j.fertnstert.2010.02.013. Epub 2010 Mar 24. Fertil Steril. 2010. PMID: 20338563 Free article.

2

Mosaic ring Y chromosome in two normal healthy men with azoospermia.

Bertini V, Canale D, Bicocchi MP, Simi P, Valetto A. Bertini V, et al. Among authors: bicocchi mp. Fertil Steril. 2005 Dec;84(6):1744. doi: 10.1016/j.fertnstert.2005.06.034. Fertil Steril. 2005. PMID: 16359976 Free article.

3

A new strategy for prenatal diagnosis in a sporadic haemophilia B family.

Acquila M, Bottini F, Valetto A, Caprino D, Mori PG, Bicocchi MP. Acquila M, et al. Among authors: bicocchi mp. Haemophilia. 2001 Jul;7(4):416-8. doi: 10.1046/j.1365-2516.2001.00514.x. Haemophilia. 2001. PMID: 11442646

4

Inversion mutation as a major cause of severe hemophilia A in Italian patients.

Mori PG, Caprino D, Bicocchi MP, Valetto A, Bottini F, Aquila M. Mori PG, et al. Among authors: bicocchi mp. Haematologica. 1997 Jan-Feb;82(1):75-6. Haematologica. 1997. PMID: 9107090

5

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.

Acquila M, Bicocchi MP, Mori PG, Odino S, Valetto A, Bottini F. Acquila M, et al. Among authors: bicocchi mp. Eur J Haematol. 2000 Jul;65(1):80-1. doi: 10.1034/j.1600-0609.2000.9l140.x. Eur J Haematol. 2000. PMID: 10914946 No abstract available.

6

Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patient.

Giacomo Consalez G, Gecz J, Stayton CL, Dabovic B, Pasini B, Pezzolo A, Bicocchi MP, Fontes M, Romeo G. Giacomo Consalez G, et al. Among authors: bicocchi mp. Genomics. 1992 Nov;14(3):557-61. doi: 10.1016/s0888-7543(05)80151-x. Genomics. 1992. PMID: 1427884

7

Unusual presentation of haemophilia in two paediatric patients.

De Luca M, Carducci FI, Pansini V, Coletti V, Tucci FM, Cirillo M, Acquila M, Bicocchi MP, D'Argenio P, Luciani M. De Luca M, et al. Among authors: bicocchi mp. Blood Coagul Fibrinolysis. 2013 Sep;24(6):645-8. doi: 10.1097/MBC.0b013e32835fad85. Blood Coagul Fibrinolysis. 2013. PMID: 23492911

8

Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease.

Luo Y, Ceccherini I, Pasini B, Matera I, Bicocchi MP, Barone V, Bocciardi R, Kääriäinen H, Weber D, Devoto M, et al. Luo Y, et al. Among authors: bicocchi mp. Hum Mol Genet. 1993 Nov;2(11):1803-8. doi: 10.1093/hmg/2.11.1803. Hum Mol Genet. 1993. PMID: 7904208

9

Analysis of 18 novel mutations in the factor VIII gene.

Bicocchi MP, Pasino M, Lanza T, Bottini F, Boeri E, Mori PG, Molinari AC, Rosano C, Acquila M. Bicocchi MP, et al. Br J Haematol. 2003 Sep;122(5):810-7. doi: 10.1046/j.1365-2141.2003.04494.x. Br J Haematol. 2003. PMID: 12930394 Free article.

10

Mutation analysis impact on the genetic counseling of sporadic hemophilia B families.

Bicocchi MP, Pasino M, Bottini F, Lanza T, Mori PG, Acquila M. Bicocchi MP, et al. Am J Med Genet A. 2003 May 1;118A(4):328-31. doi: 10.1002/ajmg.a.20016. Am J Med Genet A. 2003. PMID: 12687663

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