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Multiple spinal ganglioneuromas in a patient harboring a pathogenic NF1 mutation

Clinical genetics, 2010-03, Vol.77 (3), p.293-297

2010

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Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X

Journal of medical genetics, 2005-08, Vol.42 (8), p.e52-e52

2005

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High-Resolution Melting Analysis for Rapid Detection of KRAS, BRAF, and PIK3CA Gene Mutations in Colorectal Cancer

American journal of clinical pathology, 2008-08, Vol.130 (2), p.247-253

2008

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Malignant extra-adrenal pheochromocytoma caused by an SDHB intronic variation leading to a 54-bp deletion in exon 4

Journal of endocrinological investigation, 2009-02, Vol.32 (2), p.111-114

2009

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Imaging of somatostatin receptors by indium-111-pentetreotide correlates with quantitative determination of somatostatin receptor type 2 gene expression in neuroblastoma tumors

Clinical cancer research, 1997-12, Vol.3 (12), p.2385-2391

1997

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Retrospective Evaluation of c-erbB-2 Oncogene Amplification using Competitive PCR in Collecting Duct Carcinoma of the Kidney

The Journal of urology, 1997-07, Vol.158 (1), p.245-247

1997

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Quantitation of somatostatin receptor type 2 gene expression in neuroblastoma cell lines and primary tumors using competitive reverse transcription-polymerase chain reaction

Clinical cancer research, 1996-10, Vol.2 (10), p.1757-1765

1996

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Premature ovarian failure and fragile X premutation: a study on 45 women

European journal of obstetrics & gynecology and reproductive biology, 2004-02, Vol.112 (2), p.189-191

2004

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An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene

Journal of neurology, neurosurgery and psychiatry, 2003-06, Vol.74 (6), p.825-826

2003

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Analysis of SAS gene and CDK4 and MDM2 proteins in low-grade osteosarcoma

Cancer detection and prevention, 1999-01, Vol.23 (2), p.129-136

1999

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Susceptibility to refractory ulcerative colitis is associated with polymorphism in the hMLH1 mismatch repair gene

Inflammatory bowel diseases, 2004-11, Vol.10 (6), p.705-708

2004

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Perception of dyspnea during exercise-induced bronchoconstriction

Respiratory medicine, 2003-03, Vol.97 (3), p.221-227

2003

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Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene

Human genetics, 2000-10, Vol.107 (4), p.366-371

2000

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Adenosine triphosphate release by osmotic shock and hemoglobin A1C in diabetic subjects' erythrocytes

Metabolism, clinical and experimental, 1994-04, Vol.43 (4), p.435-440

1994

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Serum interleukin 6 is predictive of early functional decline and mortality in interstitial lung disease associated with systemic sclerosis

Journal of rheumatology, 2013-04, Vol.40 (4), p.435-446

2013

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New positron emission tomography derived parameters as predictive factors for recurrence in resected stage I non-small cell lung cancer

European journal of surgical oncology, 2013-11, Vol.39 (11), p.1254-1261

2013

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Nonlinear laser imaging of skin lesions

Journal of biophotonics, 2008-03, Vol.1 (1), p.62-73

2008

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High levels of homocysteine, lipoprotein (a) and plasminogen activator inhibitor-1 are present in patients with abdominal aortic aneurysm

Thrombosis and haemostasis, 2005-11, Vol.94 (5), p.1094-1098

2005

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Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm

Journal of medical genetics, 2008-11, Vol.45 (11), p.721-730

2008

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Inhaled PGE2 prevents aspirin-induced bronchoconstriction and urinary LTE4 excretion in aspirin-sensitive asthma

American journal of respiratory and critical care medicine, 1996-02, Vol.153 (2), p.572-575

1996

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Interstitial Vascularity in Fibrosing Alveolitis

American journal of respiratory and critical care medicine, 2003-02, Vol.167 (3), p.438-443

2003

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Low protein Z plasma levels are independently associated with acute coronary syndromes

Thrombosis and haemostasis, 2003-12, Vol.90 (6), p.1173-1178

2003

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Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma

Human molecular genetics, 2006-09, Vol.15 (18), p.2682-2689

2006

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Thrombophilic risk factors in patients with severe carotid atherosclerosis

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.502-507

2005

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Comparison of Baseline–Nitrate Technetium-99m Sestamibi With Rest–Redistribution Thallium-201 Tomography in Detecting Viable Hibernating Myocardium and Predicting Postrevascularization Recovery

Journal of the American College of Cardiology, 1997-08, Vol.30 (2), p.384-391

1997

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Multiple spinal ganglioneuromas in a patient harboring a pathogenic NF1 mutation

Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X

High-Resolution Melting Analysis for Rapid Detection of KRAS, BRAF, and PIK3CA Gene Mutations in Colorectal Cancer

Malignant extra-adrenal pheochromocytoma caused by an SDHB intronic variation leading to a 54-bp deletion in exon 4

Imaging of somatostatin receptors by indium-111-pentetreotide correlates with quantitative determination of somatostatin receptor type 2 gene expression in neuroblastoma tumors

Retrospective Evaluation of c-erbB-2 Oncogene Amplification using Competitive PCR in Collecting Duct Carcinoma of the Kidney

Quantitation of somatostatin receptor type 2 gene expression in neuroblastoma cell lines and primary tumors using competitive reverse transcription-polymerase chain reaction

Premature ovarian failure and fragile X premutation: a study on 45 women

An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene

Analysis of SAS gene and CDK4 and MDM2 proteins in low-grade osteosarcoma

Susceptibility to refractory ulcerative colitis is associated with polymorphism in the hMLH1 mismatch repair gene

Perception of dyspnea during exercise-induced bronchoconstriction

Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene

Adenosine triphosphate release by osmotic shock and hemoglobin A1C in diabetic subjects' erythrocytes

Serum interleukin 6 is predictive of early functional decline and mortality in interstitial lung disease associated with systemic sclerosis

New positron emission tomography derived parameters as predictive factors for recurrence in resected stage I non-small cell lung cancer

Nonlinear laser imaging of skin lesions

High levels of homocysteine, lipoprotein (a) and plasminogen activator inhibitor-1 are present in patients with abdominal aortic aneurysm

Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm

Inhaled PGE2 prevents aspirin-induced bronchoconstriction and urinary LTE4 excretion in aspirin-sensitive asthma

Interstitial Vascularity in Fibrosing Alveolitis

Low protein Z plasma levels are independently associated with acute coronary syndromes

Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma

Thrombophilic risk factors in patients with severe carotid atherosclerosis

Comparison of Baseline–Nitrate Technetium-99m Sestamibi With Rest–Redistribution Thallium-201 Tomography in Detecting Viable Hibernating Myocardium and Predicting Postrevascularization Recovery

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