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Detection of EGFR alterations in circulating tumor DNA of non-small cell lung cancer by digital PCR and Next Generation Sequencing

Annals of oncology, 2015-10, Vol.26, p.vi79

2015

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Epidemiology and prevention of domestic injuries among children in the Verona area (north-east Italy)

Annali di igiene, 2002-11, Vol.14 (6), p.495

2002

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Disinfection and sterilization: methodologies and indications

Annali di igiene, 2001-01, Vol.13 (1 Suppl 2), p.29

2001

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CircRNAs in hematopoiesis and hematological malignancies

Blood cancer journal (New York), 2016-10, Vol.6 (10), p.e483-e483

2016

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Use of Invasive Brain-Computer Interfaces in Pediatric Neurosurgery: Technical and Ethical Considerations

Journal of Child Neurology, 2023-03, Vol.38 (3-4), p.223-238

2023

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Human mutation, 2013-09, Vol.34 (9), p.1208-1215

2013

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Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5

Journal of Virology, 2001-09, Vol.75 (18), p.8772-8780

2001

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DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease

Annals of neurology, 2016-02, Vol.79 (2), p.244-256

2016

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Invasive Brain Computer Interface for Motor Restoration in Spinal Cord Injury: A Systematic Review

Neuromodulation (Malden, Mass.), 2024-06, Vol.27 (4), p.597-603

2024

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ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

Neurology, 2007-05, Vol.68 (19), p.1557

2007

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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Brain (London, England : 1878), 2014-05, Vol.137 (5), p.1361-1373

2014

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Heparan Sulfate Glycosaminoglycans Are Involved in Adenovirus Type 5 and 2-Host Cell Interactions

Virology (New York, N.Y.), 2000-03, Vol.268 (2), p.382-390

2000

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Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

Journal of cystic fibrosis, 2008-09, Vol.7 (5), p.347-351

2008

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Failure of aldosterone suppression despite angiotensin-converting enzyme (ACE) inhibitor administration in chronic heart failure is associated with ACE DD genotype

Journal of the American College of Cardiology, 2001-06, Vol.37 (7), p.1808-1812

2001

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Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

European journal of human genetics : EJHG, 2006-03, Vol.14 (3), p.322-331

2006

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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis

Human mutation, 2001-08, Vol.18 (2), p.166-166

2001

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Evaluating psychiatric morbidity in a general hospital: a two-phase epidemiological survey

Psychological medicine, 1999-07, Vol.29 (4), p.823-831

1999

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Community-based mental health care: to what extent are service costs associated with clinical, social and service history variables?

Psychological medicine, 2000-09, Vol.30 (5), p.1205-1215

2000

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Mortality Among Patients with Psychiatric Illness a Ten-Year Case Register Study in an Area with a Community-based System of Care

British journal of psychiatry, 1995-06, Vol.166 (6), p.783-788

1995

Volltextzugriff (PDF)

Collecting psychiatric resources utilisation data to calculate costs of care : a comparison between a service receipt interview and a case register

Social Psychiatry and Psychiatric Epidemiology, 1999-10, Vol.34 (10), p.541-547

1999

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GIGYF2 mutations are not a frequent cause of familial Parkinson's disease

Parkinsonism & related disorders, 2009-11, Vol.15 (9), p.703-705

2009

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Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations

Human mutation, 1997, Vol.10 (2), p.135-154

1997

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Highly preferential association of NonF508del CF mutations with the M470 allele

Journal of cystic fibrosis, 2007-01, Vol.6 (1), p.15-22

2007

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A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease

Human genetics, 2001-06, Vol.108 (6), p.504-510

2001

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Detection of EGFR alterations in circulating tumor DNA of non-small cell lung cancer by digital PCR and Next Generation Sequencing

Epidemiology and prevention of domestic injuries among children in the Verona area (north-east Italy)

Disinfection and sterilization: methodologies and indications

CircRNAs in hematopoiesis and hematological malignancies

Use of Invasive Brain-Computer Interfaces in Pediatric Neurosurgery: Technical and Ethical Considerations

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5

DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease

Invasive Brain Computer Interface for Motor Restoration in Spinal Cord Injury: A Systematic Review

ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Heparan Sulfate Glycosaminoglycans Are Involved in Adenovirus Type 5 and 2-Host Cell Interactions

Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum

Failure of aldosterone suppression despite angiotensin-converting enzyme (ACE) inhibitor administration in chronic heart failure is associated with ACE DD genotype

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis

Evaluating psychiatric morbidity in a general hospital: a two-phase epidemiological survey

Community-based mental health care: to what extent are service costs associated with clinical, social and service history variables?

Mortality Among Patients with Psychiatric Illness a Ten-Year Case Register Study in an Area with a Community-based System of Care

Collecting psychiatric resources utilisation data to calculate costs of care : a comparison between a service receipt interview and a case register

GIGYF2 mutations are not a frequent cause of familial Parkinson's disease

Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations

Highly preferential association of NonF508del CF mutations with the M470 allele

A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease

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