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CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma

Cancer letters, 2016-08, Vol.378 (2), p.120-130

2016

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Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations

Clinical genetics, 2011-04, Vol.79 (4), p.345-354

2011

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Pulmonary features of Birt-Hogg-Dubé syndrome: Cystic lesions and pulmonary histiocytoma

Respiratory medicine, 2011-05, Vol.105 (5), p.768-774

2011

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Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotype

Clinical genetics, 2014-02, Vol.85 (2), p.201-202

2014

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Somatic mutations of the MET oncogene are selected during metastatic spread of human HNSC carcinomas

Oncogene, 2000-03, Vol.19 (12), p.1547-1555

2000

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CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation

Andrologia, 2010-10, Vol.42 (5), p.326-330

2010

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Birt-Hogg-Dubé syndrome (BHDS)

Atlas of genetics and cytogenetics in oncology and haematology, 2014-06 (7)

2014

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Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists

Oncogene, 1999-09, Vol.18 (37), p.5221-5231

1999

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Primary hyperparathyroidism and Klinefelter's syndrome in a young man

Endocrinology, diabetes & metabolism case reports, 2015-04, Vol.2015, p.150019-150019

2015

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Src-mediated activation of α-diacylglycerol kinase is required for hepatocyte growth factor-induced cell motility

The EMBO journal, 2000-09, Vol.19 (17), p.4614-4622

2000

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Different point mutations in the met oncogene elicit distinct biological properties

The FASEB journal, 2000-02, Vol.14 (2), p.399-406

2000

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P.152 ANALYSIS OF CFTR, SPINK1 AND PRSS1 MUTATIONS IN ITALIAN PATIENTS WITH CHRONIC PANCREATITIS

Digestive and liver disease, 2010, Vol.42, p.S156-S157

2010

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Expression of functional tyrosine kinases on immortalized Kaposi's sarcoma cells

Journal of cellular physiology, 2000-08, Vol.184 (2), p.246-254

2000

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The Association of Nutrition Status Expressed as Body Mass Index z Score With Outcomes in Children With Severe Sepsis: A Secondary Analysis From the Sepsis Prevalence, Outcomes, and Therapies (SPROUT) Study

Critical care medicine, 2018-11, Vol.46 (11), p.e1029-e1039

2018

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Bedside Ultrasonography (US), Echoscopy and US Point of Care as a new kind of stethoscope for Internal Medicine Departments: the training program of the Italian Internal Medicine Society (SIMI)

Internal and emergency medicine, 2014-10, Vol.9 (7), p.805-814

2014

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CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation: CHARGE syndrome and hypogonadism

Andrologia, 2010-10, Vol.42 (5), p.326-330

2010

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Virtual Dynamic Mechanical Analysis

Challenges in Mechanics of Time Dependent Materials, Volume 2, 2021, p.83-88

2021

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HGF controls branched morphogenesis in tubular glands

European journal of morphology, 1998-08, Vol.36 Suppl, p.74-81

1998

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Hepatocyte growth factor sensitizes human ovarian carcinoma cell lines to paclitaxel and cisplatin

Cancer research (Chicago, Ill.), 2004-03, Vol.64 (5), p.1744-1750

2004

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Proportion of patients needing an implantable cardioverter defibrillator on the basis of current guidelines: impact on healthcare resources in Italy and the USA. Data from the ALPHA study registry

Europace (London, England), 2010-08, Vol.12 (8), p.1105-1111

2010

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Amplification of repeat-containing transcribed sequences (ARTS): a transcriptome fingerprinting strategy to detect functionally relevant microsatellite mutations in cancer

Nucleic acids research, 2003-04, Vol.31 (7), p.e33-33

2003

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AN ANALYSIS OF THE TWO-DIMENSIONAL TURBULENT BUOYANT JET

Chemical engineering communications, 1989-01, Vol.81 (1), p.1-14

1989

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Somatic mutations of the METoncogene are selected during metastatic spread of human HNSC carcinomas

Oncogene, 2000-03, Vol.19 (12), p.1547

2000

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CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation

Andrologia, 2010, Vol.42 (5), p.326-330

2010

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CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma

Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations

Pulmonary features of Birt-Hogg-Dubé syndrome: Cystic lesions and pulmonary histiocytoma

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes

Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotype

Somatic mutations of the MET oncogene are selected during metastatic spread of human HNSC carcinomas

CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation

Birt-Hogg-Dubé syndrome (BHDS)

Mutant Met-mediated transformation is ligand-dependent and can be inhibited by HGF antagonists

Primary hyperparathyroidism and Klinefelter's syndrome in a young man

Src-mediated activation of α-diacylglycerol kinase is required for hepatocyte growth factor-induced cell motility

Different point mutations in the met oncogene elicit distinct biological properties

P.152 ANALYSIS OF CFTR, SPINK1 AND PRSS1 MUTATIONS IN ITALIAN PATIENTS WITH CHRONIC PANCREATITIS

Expression of functional tyrosine kinases on immortalized Kaposi's sarcoma cells

The Association of Nutrition Status Expressed as Body Mass Index z Score With Outcomes in Children With Severe Sepsis: A Secondary Analysis From the Sepsis Prevalence, Outcomes, and Therapies (SPROUT) Study

Bedside Ultrasonography (US), Echoscopy and US Point of Care as a new kind of stethoscope for Internal Medicine Departments: the training program of the Italian Internal Medicine Society (SIMI)

CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation: CHARGE syndrome and hypogonadism

Virtual Dynamic Mechanical Analysis

HGF controls branched morphogenesis in tubular glands

Hepatocyte growth factor sensitizes human ovarian carcinoma cell lines to paclitaxel and cisplatin

Proportion of patients needing an implantable cardioverter defibrillator on the basis of current guidelines: impact on healthcare resources in Italy and the USA. Data from the ALPHA study registry

Amplification of repeat-containing transcribed sequences (ARTS): a transcriptome fingerprinting strategy to detect functionally relevant microsatellite mutations in cancer

AN ANALYSIS OF THE TWO-DIMENSIONAL TURBULENT BUOYANT JET

Somatic mutations of the METoncogene are selected during metastatic spread of human HNSC carcinomas

CHARGE syndrome as unusual cause of hypogonadism: endocrine and molecular evaluation

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