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Molecular characterization of an Italian series of sporadic GISTs

Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2013-10, Vol.16 (4), p.596-601

2013

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SOD1 mutations in amyotrophic lateral sclerosis : Results from a multicenter Italian study

Journal of neurology, 2005-07, Vol.252 (7), p.782-788

2005

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GIST mutational status and survival

European journal of surgical oncology, 2013-09, Vol.39 (9), p.S57-S57

2013

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Identifcation of the Nramp Gene in TV-I fibroblasts from Turbot Psetta maxima, formerly Scophthalmus maximus L. I758 (Pisces: scophthalmidae)

Journal of biological research (Catanzaro), 2010-01, Vol.83 (1)

2010

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Genetic counselling in ALS: facts, uncertainties and clinical suggestions

Journal of Neurology, Neurosurgery and Psychiatry, 2014-05, Vol.85 (5), p.478-485

2014

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Novel MC1R variants in Ligurian melanoma patients and controls

Human mutation, 2004-07, Vol.24 (1), p.103-103

2004

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Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma

American journal of medical genetics, 2003-05, Vol.118A (4), p.309-313

2003

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Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases

Molecular and cellular probes, 1993-10, Vol.7 (5), p.415-418

1993

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Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test

Journal of the neurological sciences, 2003-08, Vol.212 (1), p.75-78

2003

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Mutation analysis of oxisterol-binding-protein gene in patients with age-related macular degeneration

Genetic testing, 2007-12, Vol.11 (4), p.421-426

2007

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Search for loss of heterozygosity and mutation analysis of KRIT1 gene in CCM patients

American journal of medical genetics, 2004-09, Vol.130A (1), p.98-101

2004

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The Genoa experience of prenatal diagnosis in NF1

Prenatal diagnosis, 2000-09, Vol.20 (9), p.719-724

2000

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Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant

Clinical genetics, 1995-06, Vol.47 (6), p.281-284

1995

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Early and long term follow-up with minisatellite probes in bone marrow transplanted patients

Leukemia, 1990-10, Vol.4 (10), p.704-707

1990

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Expression and Genomic Configuration of GM-CSF, IL-3, M-CSF Receptor (C-FMS), Early Growth Response Gene-1 (EGR-1) and M-CSF Genes in Primary Myelodysplastic Syndromes

Leukemia & lymphoma, 1994, Vol.15 (1-2), p.135-141

1994

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Amplification of c- myc and pvt-1 homologous sequences in acute nonlymphatic leukemia

Leukemia research, 1988, Vol.12 (6), p.523-527

1988

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Linkage studies in Italian families with familial adenomatous polyposis

Human genetics, 1993, Vol.90 (5), p.545-550

1993

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An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation

Amyotrophic lateral sclerosis, 2003-09, Vol.4 (3), p.167-170

2003

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Amplification of c-myc and put-1 homologous sequences in acute nonlymphatic leukemia

Leukemia research, 1988, Vol.12 (6), p.523-527

1988

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Involvement of chromosomal region 9q34 in a case of variant Ph1 translocation t(22;22)

Leukemia research, 1986, Vol.10 (9), p.1131-1137

1986

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Molecular analysis of Philadelphia-negative myeloproliferative syndromes with i(17q)

Cancer genetics and cytogenetics, 1989-12, Vol.43 (2), p.195-201

1989

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Translocation t(9;9)(p13;q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangement

Cancer genetics and cytogenetics, 1989-11, Vol.43 (1), p.51-56

1989

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Translation t(9; 9)(p13; q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangement

Cancer genetics and cytogenetics, 1989-01, Vol.43 (1), p.51-56

1989

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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.784-793

2012

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Clinicopathologic and genetic analysis of siblings with NF1 and adult-onset gliomas

Journal of the neurological sciences, 2006-08, Vol.247 (1), p.105-108

2006

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Molecular characterization of an Italian series of sporadic GISTs

SOD1 mutations in amyotrophic lateral sclerosis : Results from a multicenter Italian study

GIST mutational status and survival

Identifcation of the Nramp Gene in TV-I fibroblasts from Turbot Psetta maxima, formerly Scophthalmus maximus L. I758 (Pisces: scophthalmidae)

Genetic counselling in ALS: facts, uncertainties and clinical suggestions

Novel MC1R variants in Ligurian melanoma patients and controls

Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma

Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases

Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test

Mutation analysis of oxisterol-binding-protein gene in patients with age-related macular degeneration

Search for loss of heterozygosity and mutation analysis of KRIT1 gene in CCM patients

The Genoa experience of prenatal diagnosis in NF1

Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant

Early and long term follow-up with minisatellite probes in bone marrow transplanted patients

Expression and Genomic Configuration of GM-CSF, IL-3, M-CSF Receptor (C-FMS), Early Growth Response Gene-1 (EGR-1) and M-CSF Genes in Primary Myelodysplastic Syndromes

Amplification of c- myc and pvt-1 homologous sequences in acute nonlymphatic leukemia

Linkage studies in Italian families with familial adenomatous polyposis

An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation

Amplification of c-myc and put-1 homologous sequences in acute nonlymphatic leukemia

Involvement of chromosomal region 9q34 in a case of variant Ph1 translocation t(22;22)

Molecular analysis of Philadelphia-negative myeloproliferative syndromes with i(17q)

Translocation t(9;9)(p13;q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangement

Translation t(9; 9)(p13; q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangement

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

Clinicopathologic and genetic analysis of siblings with NF1 and adult-onset gliomas

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