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A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning

Molecular cytogenetics, 2017-06, Vol.10 (1), p.22-7, Article 22

2017

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The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

Leukemia, 2014-06, Vol.28 (6), p.1377-1379

2014

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The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

Leukemia, 2014-06, Vol.28 (6), p.1380-1380

2014

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6131 POSTER Evaluation of BRAF Mutational Status in Wild Type (WT) KRAS Metastatic Colon-Rectal Cancer (MCRC) Patients (pts) Treated With Cetuximab (C) – a Single Institution Experience

European journal of cancer (1990), 2011, Vol.47, p.S431-S431

2011

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Novel human pathological mutations. Gene symbol: ALPL. Disease: hypophosphatasia

Human genetics, 2009-04, Vol.125 (3), p.334-334

2009

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Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families

Blood, 1998-10, Vol.92 (7), p.2353-2358

1998

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Erratum: The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

Leukemia, 2014-06, Vol.28 (6), p.1380-1380

2014

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The role of PAX5 and C/EBP [alpha]/[beta] in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

Leukemia, 2014-06, Vol.28 (6), p.1380

2014

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The role of PAX5 and C/EBP [alpha] / [beta] in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

Leukemia, 2014-06, Vol.28 (6), p.1377

2014

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A nomenclature system for metabolic gene polymorphisms

IARC scientific publications, 1999 (148), p.5

1999

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Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis

Prenatal diagnosis, 2001-10, Vol.21 (10), p.801-805

2001

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Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease

Neurological sciences, 2001-02, Vol.22 (1), p.65-66

2001

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Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer

Neuromuscular disorders : NMD, 1995-07, Vol.5 (4), p.291-295

1995

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Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis

International journal of cancer, 2003-11, Vol.107 (3), p.493-497

2003

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Re: "Validated questionnaire for the identification of previous personal or familial venous thromboembolism"

American journal of epidemiology, 1998-03, Vol.147 (6), p.605-606

1998

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Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories

Genetics in medicine, 2005-11, Vol.7 (9), p.620-625

2005

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Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature

Prenatal diagnosis, 2005-02, Vol.25 (2), p.140-147

2005

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An HLA haplotype with a deletion at the HLA-A locus: A case report

Genes and immunity, 2005-04, Vol.6, p.S20-S20

2005

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Cimetidine treatment in hyper-IgM hypogammaglobulinemia

JAMA : the journal of the American Medical Association, 1987-10, Vol.258 (14), p.1892

1987

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Signal transduction in human tumor infiltrating lymphocytes

Archivum Immunologiae et Therapiae Experimentalis, 1993, Vol.41 (1), p.33-39

1993

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Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia

Leukemia research, 2000-11, Vol.24 (11), p.971-974

2000

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Appropriateness of hospital use: Report from an Italian study

European journal of public health, 1997-03, Vol.7 (1), p.34-39

1997

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Impairment of lymphocyte-suppressive system in recent-onset insulin-dependent diabetes mellitus. Correlation with metabolic control

Diabetes (New York, N.Y.), 1986-09, Vol.35 (9), p.1053

1986

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Central nervous system involvement in elderly patients with non-insulin-dependent diabetes mellitus

Acta Diabetologica Latina, 1990-10, Vol.27 (4), p.343-348

1990

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RE: “VALIDATED QUESTONNAIRE FOR THE INDENTIFICATION OF PREVIOUS PERSONAL OR FAMILAL VENOUS THROMBOEMBOLISM

American journal of epidemiology, 1998-03, Vol.147 (6), p.605-606

1998

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A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning

The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

6131 POSTER Evaluation of BRAF Mutational Status in Wild Type (WT) KRAS Metastatic Colon-Rectal Cancer (MCRC) Patients (pts) Treated With Cetuximab (C) – a Single Institution Experience

Novel human pathological mutations. Gene symbol: ALPL. Disease: hypophosphatasia

Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families

Erratum: The role of PAX5 and C/EBP α/β in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

The role of PAX5 and C/EBP [alpha]/[beta] in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

The role of PAX5 and C/EBP [alpha] / [beta] in atypical non-Langerhans cell histiocytic tumor post acute lymphoblastic leukemia

A nomenclature system for metabolic gene polymorphisms

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis

Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease

Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis

Re: "Validated questionnaire for the identification of previous personal or familial venous thromboembolism"

Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories

Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature

An HLA haplotype with a deletion at the HLA-A locus: A case report

Cimetidine treatment in hyper-IgM hypogammaglobulinemia

Signal transduction in human tumor infiltrating lymphocytes

Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia

Appropriateness of hospital use: Report from an Italian study

Impairment of lymphocyte-suppressive system in recent-onset insulin-dependent diabetes mellitus. Correlation with metabolic control

Central nervous system involvement in elderly patients with non-insulin-dependent diabetes mellitus

RE: “VALIDATED QUESTONNAIRE FOR THE INDENTIFICATION OF PREVIOUS PERSONAL OR FAMILAL VENOUS THROMBOEMBOLISM

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