M. Bicocchi

发表

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

J. Gécz, B. Pasini, G. Romeo, 1992, Genomics.

Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10

G. Gimelli, A. Puliti, G. Romeo, 1992, Pediatric Surgery International.

Epidemiological Findings on the Prevalence of Dysuria and Benign Prostatic Hypertrophy in 7303 Patients over 50 Years Old

M. Bicocchi, G. Mauceri, M. Fini, 1994 .

Exon skipping partially restores factor VIII coagulant activity in patients with mild hemophilia A with exon 13 duplication.

C. Rosano, M. Bicocchi, A. Molinari, 2005, Haematologica.

Diagnostic potential of hepcidin testing in pediatrics

A. Martini, A. Pistorio, M. Bicocchi, 2013, European journal of haematology.

Unusual presentation of haemophilia in two paediatric patients.

P. D’argenio, M. Bicocchi, M. Luciani, 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype

M. Margaglione, E. Grandone, F. Torricelli, 2008, Haematologica.

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

M. Bicocchi, M. Pasino, P. Mori, 2003, American journal of medical genetics. Part A.

A novel point mutation in severe haemophilia A: a further proof of genotype‐phenotype correlation

M. Bicocchi, A. Borchiellini, M. Acquila, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Prenatal diagnosis of haemophilia B: the Italian experience

M. Bicocchi, I. Garagiola, A. Rocino, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Mutation analysis is an essential strategy in the genetic counselling of sporadic haemophilia B families

M. Bicocchi, M. Pasino, T. Lanza, 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

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

M. Bicocchi, D. Caprino, P. Mori, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

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

P. Simi, M. Bicocchi, D. Canale, 2005, Fertility and sterility.

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

M. Bicocchi, D. Caprino, P. Mori, 1997, Haematologica.

Ectopic mRNA analysis and molecular modelling substantiate severe haemophilia in a patient with a FVIII gene splice mutation

C. Rosano, M. Bicocchi, A. Molinari, 2005, Thrombosis and Haemostasis.

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

M. Devoto, B. Pasini, R. Bocciardi, 1993, Human molecular genetics.

Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection.

A. Covone, A. Puliti, G. Romeo, 1993, Cytogenetics and cell genetics.

Duplication of exon 13 causes one third of the cases of mild hemophilia A in northern Italy.

M. Bicocchi, A. Molinari, M. Pasino, 2004, Haematologica.

MLPA assay in F8 gene mutation screening

M. Bicocchi, A. Molinari, M. Pasino, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

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

P. Simi, M. Bicocchi, P. Ghirri, 2010, Fertility and sterility.

Three-year longitudinal study with quantitative ultrasound at the hand phalanx in a female population

M. Bicocchi, R. Cadossi, V. Ventura, 2007, Osteoporosis International.

Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A

B. Migeon, F. Corsolini, M. Bicocchi, 2005, European Journal of Human Genetics.

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

M. Bicocchi, D. Caprino, P. Mori, 2001 .

Small FVIII gene rearrangements in 18 hemophilia A patients: Five novel mutations

C. Rosano, M. Bicocchi, A. Molinari, 2005, American journal of hematology.

Numerical and structural aberrations in advanced neuroblastoma tumours by CGH analysis; survival correlates with chromosome 17 status

G. Tonini, C. L. Cunsolo, M. Bicocchi, 2000, British Journal of Cancer.

Frequency of factor VIII intron 1 inversion in a cohort of severe hemophilia A Italian patients.

M. Bicocchi, M. Pasino, T. Lanza, 2003, Haematologica.

Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia A

M. Bicocchi, A. Molinari, M. Pasino, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Analysis of 18 novel mutations in the factor VIII gene

C. Rosano, M. Bicocchi, A. Molinari, 2003, British journal of haematology.

Germ‐line origin of intron 1 inversion in two haemophilia A families

C. Santoro, M. Bicocchi, M. Pasino, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

Replacement of the Y450 (c234) phenyl ring in the carboxyl-terminal region of coagulation factor IX causes pleiotropic effects on secretion and enzyme activity

F. Bernardi, M. Pinotti, A. Branchini, 2013, FEBS letters.

Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation

C. Rosano, M. Bicocchi, M. Acquila, 2013, European journal of haematology.

De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.

M. Bicocchi, G. Serra, C. Cuoco, 1990, American journal of medical genetics.

Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B

C. Rosano, M. Bicocchi, M. Acquila, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Molecular analysis of severe factor XI deficiency in three Italian patients

M. Bicocchi, L. Banov, M. Acquila, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Frequency of factor VIII intron 1 inversion in a cohort of severe hemophilia A Italian patients.

M. Bicocchi, M. Pasino, M. Acquila, 2003 .