Márcio Cardoso

Clinical 3-D Gait Assessment of Patients With Polyneuropathy Associated With Hereditary Transthyretin Amyloidosis

Ana Patrícia Rocha, J. Fernandes, J. Cunha, 2020, Frontiers in Neurology.

Assessing mNIS+7Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trial

S. Ayache, R. Bergemann, W. Litchy, 2017, Muscle & nerve.

Age-dependent cognitive dysfunction in untreated hereditary transthyretin amyloidosis

J. Kelly, S. Cavaco, J. Fernandes, 2018, Journal of Neurology.

Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series

M. C. Vilas-Boas, T. Coelho, Márcio Cardoso, 2022, Journal of clinical medicine.

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

E. Nordh, Yi-Chung Lee, R. Sommerville, 2020, Lancet Neurology.

RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre.

Jorge Oliveira, T. Coelho, A. Gonçalves, 2017, Journal of neuromuscular diseases.

Portable RGB-D Camera-Based System for Assessing Gait Impairment Progression in ATTRv Amyloidosis

Ana Patrícia Rocha, J. Fernandes, J. Cunha, 2022, Applied Sciences.

LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes

J. D. den Dunnen, M. Sousa, T. Winder, 2018, Human mutation.

Predictors of cognitive dysfunction in hereditary transthyretin amyloidosis with liver transplant

A. Teixeira-Pinto, S. Cavaco, J. Fernandes, 2022, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Validation of a Single RGB-D Camera for Gait Assessment of Polyneuropathy Patients

João Paulo Silva Cunha, Maria do Carmo Vilas-Boas, Hugo Miguel Pereira Choupina, 2019, Sensors.

Supporting the Assessment of Hereditary Transthyretin Amyloidosis Patients Based On 3-D Gait Analysis and Machine Learning

Ana Patrícia Rocha, J. Fernandes, J. Cunha, 2021, IEEE transactions on neural systems and rehabilitation engineering.

An SPG7 mutation as a novel cause of monogenic progressive muscular atrophy

A. Fortuna, I. Alonso, Márcio Cardoso, 2023, Neurological Sciences.

Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy

Karla P. Zepeda, Hansie M Mathelier, J. Felius, 2023, Neurology and Therapy.

Familial Amyloid Polyneuropathy treatment with Tafamidis – evaluation of one- and two-year treatment in Porto, Portugal

T. Coelho, Márcio Cardoso, C. Alves, 2015, Orphanet Journal of Rare Diseases.