André M. Travessa

High prevalence of variants in skeletal dysplasia associated genes in individuals with short stature and minor skeletal anomalies.

F. Santos-Simarro, J. Nevado, C. de la Torre, 2021, European journal of endocrinology.

Treatment of Heart Failure With Reduced Ejection Fraction—Recent Developments

André M Travessa, L. Menezes Falcão, André M. Travessa, 2016, American journal of therapeutics.

Genetics of personalized medicine: cancer and rare diseases

Ana Rita Marques, R. Rodrigues, V. Gonçalves, 2018, Cellular Oncology.

Fifteen Years of Clinical Trials in Huntington's Disease: A Very Low Clinical Drug Development Success Rate.

J. Ferreira, T. Mestre, F. B. Rodrigues, 2017, Journal of Huntington's disease.

Vasodilators in acute heart failure - evidence based on new studies.

André M Travessa, L. Menezes Falcão, André M. Travessa, 2018, European journal of internal medicine.

Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)

A. Sinclair, J. Christodoulou, T. Stojkovic, 2020, Human Genetics.

Clinical and molecular description of 16 families with heterozygous IHH variants.

Gabriela A. Vasques, C. de la Torre, E. Vallespín, 2020, The Journal of clinical endocrinology and metabolism.

Characterization of three adults and an adolescent with Osteogenesis Imperfecta type VI and a novel founder SERPINF1 variant

K. Heath, J. Romeu, Francisca Díaz-González, 2023, European Journal of Medical Genetics.

Vosoritide Therapy in Children with Achondroplasia: Early Experience and Practical Considerations for Clinical Practice

J. Hoover-Fong, Ricki S. Carroll, E. Lausch, 2023, Advances in therapy.