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European Journal of Internal Medicine|February 28, 2018
Vasodilators in acute heart failure - evidence based on new studiesAndré M Travessa, L Menezes Falcão
Clinical Case Reports|September 29, 2025
A Case of Hereditary Spastic Paraplegia Type 50 With a Novel AP4M1 Variant and a Brief Review of the LiteratureAna Teresa Guerra, André M Travessa, José Paulo Monteiro
BMJ Case Reports|January 6, 2026
Identification of an unusual variant of Fanconi-Bickel syndrome presenting as proximal tubulopathy and short statureMadalena Roque do Vale Afonso, Paula Nunes, André M Travessa
Journal of Huntington'S Disease|July 4, 2017
Fifteen Years of Clinical Trials in Huntington's Disease: A Very Low Clinical Drug Development Success RateAndré M Travessa, Filipe B Rodrigues, Tiago A Mestre, et al.
Cureus|January 8, 2025
Periventricular Nodular Heterotopias Induced-Seizures in an AdolescentAndreia Fernandes, Mafalda J Pereira, Íris Oliveira, et al.
Parkinsonism & Related Disorders|November 25, 2019
Reporting and methodological quality of clinical trials on exercise therapy for Parkinson's diseaseCláudia M Silva, André M Travessa, Raquel Bouça-Machado, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
Upper limb phocomelia: A prenatal case of thrombocytopenia-absent radius (TAR) syndrome illustrating the importance of chromosomal microarray in limb reduction defectsAndré M Travessa, Patrícia Dias, Antónia Santos, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|January 20, 2024
Uniparental Disomy as a Mechanism for Combined Oxidative Phosphorylation Deficiency Associated with MRPS34 GeneMarta P Soares, André M Travessa, Sónia Custódio, et al.
American Journal of Medical Genetics. Part A|September 27, 2022
Precocious puberty and anal stenosis in an African patient with Rothmund-Thomson syndromeCristina Lorenzo, André M Travessa, Ana Cristóvão Ferreira, et al.
American Journal of Medical Genetics. Part A|August 29, 2020
Spondyloepiphyseal dysplasia type Stanescu: Expanding the clinical and molecular spectrum of a very rare type II collagenopathyAndré M Travessa, Francisca Díaz-González, Teresa Mirco, et al.
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