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Head-to-head comparison of ventilation/perfusion single photon emission computed tomography/computed tomography and multidetector computed tomography angiography for the detection of acute pulmonary embolism in clinical practice

Perfusion, 2023-04, Vol.38 (3), p.637-644

2023

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ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report

Case reports in endocrinology, 2020, Vol.2020 (2020), p.1-5

2020

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Spectrum of CFTR gene sequence variants in a northern Portugal population

Pulmonology, 2018-01, Vol.24 (1), p.3-9

2018

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310 Prevalence of CF and spectrum of CFTR mutations in the Portuguese population

Journal of cystic fibrosis, 2015-06, Vol.14, p.S138-S138

2015

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A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera , Figitidae)– Drosophila melanogaster interaction

Insect biochemistry and molecular biology, 2005-02, Vol.35 (2), p.93-103

2005

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6 The difficulty of the diagnosis of cystic fibrosis when a new mutation is present

Journal of cystic fibrosis, 2013-06, Vol.12, p.S49-S49

2013

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25 Analysis of CFTR gene mutations in Portuguese patients with idiopathic bronchiectasis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S54-S54

2013

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345 Study of the prevalence of CFTR gene mutations in the Portuguese population

Journal of cystic fibrosis, 2012-06, Vol.11, p.S145-S145

2012

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Quantification of CFTR IVS8(T) splice variants in CAVD patients

Journal of cystic fibrosis, 2010, Vol.9, p.S16-S16

2010

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Molecular characterization of a CAVD-causing mutation – V1108L CFTR

Journal of cystic fibrosis, 2010, Vol.9, p.S15-S15

2010

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Spectrum of CFTR mutations in northern Portugal patients with CF and related phenotypes

Journal of cystic fibrosis, 2009, Vol.8, p.S7-S7

2009

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Structural characterization of novel CBAVD-causing mutations located in CFTR NBDs

Journal of cystic fibrosis, 2008-06, Vol.7, p.S16-S16

2008

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PURA syndrome in a child with severe developmental delay: a challenging diagnosis

Revista de neurologiá, 2022-03, Vol.74 (5), p.170

2022

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25 Molecular and functional characterization of CBAVD-causing mutations located in both NBDs of the CFTR protein

Journal of cystic fibrosis, 2007, Vol.6, p.S6-S6

2007

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1ISG-028 An assessment of hospital pharmacists’ job satisfaction: application of the job satisfaction survey

European journal of hospital pharmacy. Science and practice, 2019-03, Vol.26 (Suppl 1), p.A13-A13

2019

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Adjunctive rifampicin to reduce early mortality from Staphylococcus aureus bacteraemia (ARREST): study protocol for a randomised controlled trial

Trials, 2012-12, Vol.13 (1), p.241-241, Article 241

2012

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Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

Human reproduction (Oxford), 2004-11, Vol.19 (11), p.2502-2508

2004

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A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens

Fertility and sterility, 2005-02, Vol.83 (2), p.448-451

2005

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A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae) - Drosophila melanoogaster interaction

Insect biochemistry and molecular biology, 2005, Vol.35, p.93-103

2005

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11 Complete molecular analysis of the CFTR gene in congenital absence of the vas deferens

Journal of cystic fibrosis, 2006, Vol.5, p.S3-S3

2006

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PURA syndrome in a child with severe developmental delay: a challenging diagnosis

Revista de neurologia, 2022, Vol.74 (5), p.170-173

2022

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THE ASSOCIATION AND MISDIAGNOSIS OF TUBERCULOSIS AND PARACOCCIDIOIDOMYCOSIS

Chest, 2006-10, Vol.130 (4), p.263S-263S

2006

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ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report

Case reports in endocrinology, 2020, Vol.2020, p.8848151-8848151

2020

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THE ASSOCIATION OF PARACOCCIDIOIDOMYCOSIS (PCM) WITH TUBERCULOSIS (TB)

Revista do Instituto de Medicina Tropical de São Paulo, 2005-10, Vol.47, p.37

2005

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Review of Tá rindo de quê? Humor e ditadura

European review of Latin American and Caribbean studies, 2022-11 (114), p.2

Grangeia, Mario Luis

2022

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Head-to-head comparison of ventilation/perfusion single photon emission computed tomography/computed tomography and multidetector computed tomography angiography for the detection of acute pulmonary embolism in clinical practice

ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report

Spectrum of CFTR gene sequence variants in a northern Portugal population

310 Prevalence of CF and spectrum of CFTR mutations in the Portuguese population

A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera , Figitidae)– Drosophila melanogaster interaction

6 The difficulty of the diagnosis of cystic fibrosis when a new mutation is present

25 Analysis of CFTR gene mutations in Portuguese patients with idiopathic bronchiectasis

345 Study of the prevalence of CFTR gene mutations in the Portuguese population

Quantification of CFTR IVS8(T) splice variants in CAVD patients

Molecular characterization of a CAVD-causing mutation – V1108L CFTR

Spectrum of CFTR mutations in northern Portugal patients with CF and related phenotypes

Structural characterization of novel CBAVD-causing mutations located in CFTR NBDs

PURA syndrome in a child with severe developmental delay: a challenging diagnosis

25 Molecular and functional characterization of CBAVD-causing mutations located in both NBDs of the CFTR protein

1ISG-028 An assessment of hospital pharmacists’ job satisfaction: application of the job satisfaction survey

Adjunctive rifampicin to reduce early mortality from Staphylococcus aureus bacteraemia (ARREST): study protocol for a randomised controlled trial

Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens

A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae) - Drosophila melanoogaster interaction

11 Complete molecular analysis of the CFTR gene in congenital absence of the vas deferens

PURA syndrome in a child with severe developmental delay: a challenging diagnosis

THE ASSOCIATION AND MISDIAGNOSIS OF TUBERCULOSIS AND PARACOCCIDIOIDOMYCOSIS

ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report

THE ASSOCIATION OF PARACOCCIDIOIDOMYCOSIS (PCM) WITH TUBERCULOSIS (TB)

Review of Tá rindo de quê? Humor e ditadura

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