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Function-Associated Surface Molecules on Airway Dendritic Cells in Cigarette Smokers

American journal of respiratory cell and molecular biology, 2008-06, Vol.38 (6), p.655-660

2008

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Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature

BMC cancer, 2012-06, Vol.12 (1), p.217-217, Article 217

2012

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Impact of immunotherapy on blood dendritic cells in patients with Hymenoptera venom allergy

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.487-494.e3

2011

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Pneumocystis jiroveci Dihydropteroate Synthase Gene Mutations at Codon 171 but Not at Codons 55 or 57 Detected in Germany

Clinical infectious diseases, 2006-02, Vol.42 (4), p.582-583

2006

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Primary lung carcinoma in children and adolescents – Clinical characteristics and outcome of 12 cases from the German registry for rare paediatric tumours (STEP)

Lung cancer (Amsterdam, Netherlands), 2021-10, Vol.160, p.66-72

2021

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Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

Journal of medical genetics, 2016-06, Vol.53 (6), p.419-425

2016

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Bronchoalveolar lavage for the diagnosis of Pulmonary Langerhans cell histiocytosis

Respiratory medicine, 2016-10, Vol.119, p.168-174

2016

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Spatial mapping of VOC exhalation by means of bronchoscopic sampling

Journal of breath research, 2020-10, Vol.14 (4), p.046012-046012

2020

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A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8

Journal of the neurological sciences, 2014-12, Vol.347 (1), p.372-374

2014

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Two Stage Interventional Management of Tube Thoracostomy Induced Pulmonary Artery Perforation in a Patient with Parapneumonic Pleural Effusion Associated With Oesophageal Squamous Cell Carcinoma

Heart, lung & circulation, 2017-12, Vol.26 (12), p.e121-e122

2017

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Impact of smoking on dendritic cell phenotypes in the airway lumen of patients with COPD

Respiratory research, 2014-04, Vol.15 (1), p.48-48, Article 48

2014

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Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1

European journal of human genetics : EJHG, 2008-01, Vol.16 (1), p.62-72

2008

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Fluticasone impact on airway dendritic cells in smokers: a randomized controlled trial

Respiratory research, 2013-10, Vol.14 (1), p.114-114

2013

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UMA ANÁLISE DISCURSIVA DA AVALIAÇÃO DA EXTENSÃO NA RESOLUÇÃO CNE/CES Nº 7: O BIG BROTHER

Linha Mestra, 2022-06, Vol.16 (46), p.619-631

2022

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Clinical and Mutational Spectrum of Mowat–Wilson Syndrome

European journal of medical genetics, 2005-04, Vol.48 (2), p.97-111

2005

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Absence of association between cyclin D1 ( CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer

Cancer letters, 2006-05, Vol.236 (2), p.191-197

2006

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The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

Cancer letters, 2007-07, Vol.252 (1), p.55-64

2007

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Assessment of Diagnostic Accuracy of Bronchoalveolar Lavage Cytology in the Diagnosis of Lung Tumors and Contribution to the Classification of Non-Small Cell Lung Cancer Entities: A Retrospective Clinocopathological Study

Open Journal of Pathology (Irvine CA), 2013, Vol.3 (3), p.107-112

2013

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Ten novel MSH2 and MLH1 germline mutations in families with HNPCC

Human mutation, 2004-10, Vol.24 (4), p.351-352

2004

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Ten novel MSH2 and MLH1 germline mutations in families with HNPCC: MUTATIONS IN BRIEF

Human mutation, 2004-10, Vol.24 (4), p.351-352

2004

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Identification of six novel MSH2 and MLH1 germline mutations in HNPCC

Human mutation, 2003-04, Vol.21 (4), p.445-446

2003

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Identification of six novel MSH2 and MLH1 germline mutations in HNPCC: MUTATIONS IN BRIEF

Human mutation, 2003-04, Vol.21 (4), p.445-446

2003

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Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer: Mutations in Brief

Human mutation, 2002-01, Vol.19 (1), p.82-82

2002

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Mechanism of centromere recruitment of the CENP-A chaperone HJURP and its implications for centromere licensing

Nature communications, 2019-09, Vol.10 (1), p.4046-18, Article 4046

2019

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Function-Associated Surface Molecules on Airway Dendritic Cells in Cigarette Smokers

Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature

Impact of immunotherapy on blood dendritic cells in patients with Hymenoptera venom allergy

Pneumocystis jiroveci Dihydropteroate Synthase Gene Mutations at Codon 171 but Not at Codons 55 or 57 Detected in Germany

Primary lung carcinoma in children and adolescents – Clinical characteristics and outcome of 12 cases from the German registry for rare paediatric tumours (STEP)

Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

Bronchoalveolar lavage for the diagnosis of Pulmonary Langerhans cell histiocytosis

Spatial mapping of VOC exhalation by means of bronchoscopic sampling

A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8

Two Stage Interventional Management of Tube Thoracostomy Induced Pulmonary Artery Perforation in a Patient with Parapneumonic Pleural Effusion Associated With Oesophageal Squamous Cell Carcinoma

Impact of smoking on dendritic cell phenotypes in the airway lumen of patients with COPD

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1

Fluticasone impact on airway dendritic cells in smokers: a randomized controlled trial

UMA ANÁLISE DISCURSIVA DA AVALIAÇÃO DA EXTENSÃO NA RESOLUÇÃO CNE/CES Nº 7: O BIG BROTHER

Clinical and Mutational Spectrum of Mowat–Wilson Syndrome

Absence of association between cyclin D1 ( CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

Assessment of Diagnostic Accuracy of Bronchoalveolar Lavage Cytology in the Diagnosis of Lung Tumors and Contribution to the Classification of Non-Small Cell Lung Cancer Entities: A Retrospective Clinocopathological Study

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC: MUTATIONS IN BRIEF

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC: MUTATIONS IN BRIEF

Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer: Mutations in Brief

Mechanism of centromere recruitment of the CENP-A chaperone HJURP and its implications for centromere licensing

An Agenda for Open Science in Communication

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