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Fcγ-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis

Journal of allergy and clinical immunology, 2016-05, Vol.137 (5), p.1597-1599.e8

2016

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PTPN22 R620W polymorphism in the ANCA-associated vasculitides

Rheumatology (Oxford, England), 2012-05, Vol.51 (5), p.805-812

2012

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BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study

Breast (Edinburgh), 2007-06, Vol.16 (3), p.280-292

2007

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Cryptic 13q34 and 4q35.2 Deletions in an Italian Family

Cytogenetic and genome research, 2015-01, Vol.147 (1), p.24-30

2015

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HLA–DRB4 as a genetic risk factor for Churg‐Strauss syndrome

Arthritis and rheumatism, 2007-09, Vol.56 (9), p.3159-3166

2007

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Chronic periaortitis and HLA–DRB103: Another clue to an autoimmune origin

Arthritis and rheumatism, 2006-02, Vol.55 (1), p.126-130

2006

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A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes

Breast cancer research and treatment, 2005-05, Vol.91 (2), p.203-205

2005

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Alterations of Type IV Collagen α Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss

American journal of nephrology, 2007-01, Vol.27 (2), p.129-137

2007

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Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study

Tumori, 2005-11, Vol.91 (6), p.505-512

2005

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Fc[gamma]-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis

Journal of allergy and clinical immunology, 2016-05, Vol.137 (5), p.1597

2016

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Association of HLA-DRB10401 allele with chronic pancreatitis

Pancreas, 2003-05, Vol.26 (4), p.388-391

2003

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Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas

Hereditary cancer in clinical practice, 2011-08, Vol.9 (1), p.6-6, Article 6

2011

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Multiple changes in thyroid function in patients with chronic active HCV hepatitis treated with recombinant interferon-alpha

The American journal of medicine, 1996-11, Vol.101 (5), p.482-487

1996

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Alterations of Type IV Collagen [alpha] Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss

American journal of nephrology, 2007-04, Vol.27 (2), p.129-137

2007

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The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC)

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A448-A449

2000

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HLA-DRB1 and tumor necrosis factor a but not cystic fibrosis transmembrane conductance regulator genes contribute to the genetic susceptibility of primary sclerosing cholangitis

Gastroenterology (New York, N.Y. 1943), 2001-04, Vol.120 (5), p.A573-A573

2001

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Iodine-induced subclinical hypothyroidism in euthyroid subjects with a previous episode of amiodarone-induced thyrotoxicosis

The journal of clinical endocrinology and metabolism, 1992-11, Vol.75 (5), p.1273-1277

1992

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Fine specificity of the human T-cell response to the hepatitis B virus preS1 antigen

Gastroenterology (New York, N.Y. 1943), 1992-07, Vol.103 (1), p.255-263

1992

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URINARY EXCRETION OF BRUSH-BORDER ANTIGEN REVEALED BY MONOCLONAL ANTIBODY: EARLY INDICATOR OF TOXIC NEPHROPATHY

The Lancet (British edition), 1985-10, Vol.326 (8461), p.914-917

1985

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T-cell receptor β-chain gene rearrangement and expression during human thymic ontogenesis

Blood, 1992-03, Vol.79 (6), p.1472-1483

1992

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TCR-beta chain gene rearrangement and expression in human T-cell development and in leukemia

Leukemia, 1994-06, Vol.8 (6), p.918

1994

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The contribution of MHC region genes and the mutations of the CFTR gene in the genetic predisposition to primary sclerosing cholangitis (PSC)

Digestive and liver disease, 2000-11, Vol.32, p.A121-A121

2000

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Polymorphism and Sequence Variations of the HumCD4 Pentameric Microsatellite in an Italian Population Sample

Journal of forensic sciences, 1998-07, Vol.43 (4), p.841-844

1998

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Missense mutations in the COL4A5 gene in patients with X-linked alport syndrome

Human mutation, 1998, Vol.11 (S1), p.S106-S109

1998

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Histocompatibility antigens in patients with cystic fibrosis and diabetes mellitus

The Journal of pediatrics, 1984-05, Vol.104 (5), p.799-800

1984

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Fcγ-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis

PTPN22 R620W polymorphism in the ANCA-associated vasculitides

BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: A population-based study

Cryptic 13q34 and 4q35.2 Deletions in an Italian Family

HLA–DRB4 as a genetic risk factor for Churg‐Strauss syndrome

Chronic periaortitis and HLA–DRB103: Another clue to an autoimmune origin

A breast cancer patient from Italy with germline mutations in both the BRCA1 and BRCA2 genes

Alterations of Type IV Collagen α Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss

Molecular profile and clinical variables in BRCA1-positive breast cancers. A population-based study

Fc[gamma]-receptor 3B ( FCGR3B ) copy number variations in patients with eosinophilic granulomatosis with polyangiitis

Association of HLA-DRB10401 allele with chronic pancreatitis

Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas

Multiple changes in thyroid function in patients with chronic active HCV hepatitis treated with recombinant interferon-alpha

Alterations of Type IV Collagen [alpha] Chains in Patients with Chronic Acquired Glomerulopathies: mRNA Levels, Protein Expression and Urinary Loss

The contribution of MHC region genes in the genetic predisposition to primary sclerosing cholangitis (PSC)

HLA-DRB1 and tumor necrosis factor a but not cystic fibrosis transmembrane conductance regulator genes contribute to the genetic susceptibility of primary sclerosing cholangitis

Iodine-induced subclinical hypothyroidism in euthyroid subjects with a previous episode of amiodarone-induced thyrotoxicosis

Fine specificity of the human T-cell response to the hepatitis B virus preS1 antigen

URINARY EXCRETION OF BRUSH-BORDER ANTIGEN REVEALED BY MONOCLONAL ANTIBODY: EARLY INDICATOR OF TOXIC NEPHROPATHY

T-cell receptor β-chain gene rearrangement and expression during human thymic ontogenesis

TCR-beta chain gene rearrangement and expression in human T-cell development and in leukemia

The contribution of MHC region genes and the mutations of the CFTR gene in the genetic predisposition to primary sclerosing cholangitis (PSC)

Polymorphism and Sequence Variations of the HumCD4 Pentameric Microsatellite in an Italian Population Sample

Missense mutations in the COL4A5 gene in patients with X-linked alport syndrome

Histocompatibility antigens in patients with cystic fibrosis and diabetes mellitus

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