7 documents found, page 1 of 1

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Organization of Home Mechanical Ventilation in Portugal: Characterization of Cu...

Mineiro, A; Guimarães, MJ; Winck, JC

Introduction: Home Mechanical Ventilation (HMV) is increasing worldwide. Objective: Characterization of the Portuguese HMV Units. Methods: The HMV Team Group of the Portuguese Pulmonology Society prepared a questionnaire that was sent by e-mail addressed to Pneumology Department Directors throughout the country, and the responses were then analyzed. The results enabled a provisional classification of the Units,...


Importance of Cardiac Implantable Eletronic Devices in the Diagnosis of Sleep A...

Ribeiro, S; Bonito, L; Guimarães, MJ; Português, J; Rodrigues, B; Alves, A; Durães, C; Ferreira, D; Sanfins, V; Lourenço, A

Introduction: Sleep Apnea Syndrome (SAS) is a prevalent respiratory disease with marked expression in the population with cardiovascular disease. The diagnosis is based on polysomnography. In patients with cardiac implantable electronic devices (CIED), the prevalence of SAS may reach 60%. The objective of this study was to evaluate the value of DEC in the SAS screening. Methods: Prospective study that included ...


Clinical and Molecular Markers in COPD

Gonçalves, I; Guimarães, MJ; van Zeller, M; Menezes, F; Moita, J; Simão, P

Chronic obstructive pulmonary disease (COPD) is a complex and heterogeneous disease, and there is a clinical need for validated markers and biomarkers that can contribute to the assessment of patients, risk prediction, treatment guidance, and assessment of response. Although according to the 2018 GOLD guidelines clinically useful biomarkers for COPD patients in stable condition have yet to be identified, severa...


Prevalence of Late-Onset Pompe Disease in Portuguese Patients with Diaphragmati...

Guimarães, MJ; Winck, JC; Conde, B; Mineiro, A; Raposo, M; Moita, J; Marinho, A; Silva, JM; Pires, N; André, S; Loureiro, C

Pompe disease is a rare autosomal recessive neuromuscular disorder caused by acid α-glucosidase enzyme (GAA) deficiency and divided into two distinct variants, infantile- and late-onset. The late-onset variant is characterized by a spectrum of phenotypic variation that may range from asymptomatic, to reduced muscle strength and/or diaphragmatic paralysis. Since muscle strength loss is characteristic of several ...


Pediatria do Neurodesenvolvimento. Levantamento Nacional de Recursos e Necessid...

Oliveira, G; Duque, F; Duarte, C; Melo, F; Teles, L; Brito, M; Vale, MC; Guimarães, MJ; Gouveia, R

As perturbações do neurodesenvolvimento são das patologias crónicas mais frequentes da infância e com tendência a aumentar nas sociedades modernas. Têm na grande maioria dos casos um percurso crónico e com limitação da aprendizagem necessária para a integração na sociedade de um modo autónomo. A Sociedade de Pediatria do Neurodesenvolvimento da Sociedade Portuguesa de Pediatria procedeu em 2008 e 2009 ao levant...


Pediatria do neurodesenvolvimento: levantamente nacional de recursos e necessid...

Oliveira, G; Duque, F; Duarte, C; Melo, F; Teles, L; Brito, F; Vale, MC; Guimarães, MJ; Gouveia, R


Ectopic thyroid in the anterior mediastinum

Guimarães, MJ; Valente, C; Santos, L; Baganha, MF

Ectopic thyroid is a rare condition, and its location in the anterior mediastinum is even rarer, there having been only 5 reported cases in the past 30 years. Here, we describe 2 clinical cases and present a review of the literature regarding the etiology, embryology and clinical manifestations of ectopic thyroid.


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