Joana Damásio

Instituto Universitário de Ciências da Saúde

Portugal

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Articles (16)

Year:

2024

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

Collaborators (9)

Nuno Maia

Invited associated professor

Instituto Politécnico de Leiria

PORTUGAL

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Ana do Carmo Azevedo

Centro Hospitalar de Entre o Douro e Vouga EPE

PORTUGAL

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Sara Cavaco

Head of the Neuropsychology Service

Centro Hospitalar Universitário do Porto

PORTUGAL

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Natália Oliva Teles

PORTUGAL

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Cláudia Santos Silva

Universidade de Lisboa Instituto de Medicina Molecular João Lobo Antunes

PORTUGAL

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Jorge Sequeiros

PORTUGAL

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Esmeralda Neves

Clinical Professor

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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Rui Magalhães

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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João Lemos

Auxiliary Professor

University of Coimbra

PORTUGAL

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Joana Damásio

Research Interests

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Articles (16)

Síndrome de Stiff-Person: Revisão

MultisystemicRFC1-Related Disorder

Pseudodominance in Friedreich Ataxia—Impact of High Prevalence of Carriers and Intrafamilial Clinical Variation

Gene Suppression Therapies in Hereditary Cerebellar Ataxias: A Systematic Review of Animal Studies

Peripheral neuropathy in Parkinson’s disease: prevalence and functional impact on gait and balance

<scp>Early‐Onset</scp> and Severe Complex Hereditary Spastic Paraplegia Caused by <i>De Novo</i> Variants in <i>SPAST</i>

Distinct phenotypes in a cohort of anti-CASPR2 associated neurological syndromes

Imaging in FIG 4—Related Parkinsonism

Hybrid Deep Brain Stimulation for Parkinson’s Disease and Dystonia Improves Side Effects, Maintaining Clinical Benefit

Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes

Anti-NMDAr Encephalitis and COVID-19 in a Patient With Systemic pANCA-Vasculitis and Recurrent Varicella Zoster Infection

Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia

Brain Calcifications in Complex Sexual Aneuploidy

Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype

Rare occurrence of severe blindness and deafness in Friedreich ataxia: a case report

A Case of YY1-Related Isolated Dystonia with Severe Oromandibular Involvement.

Collaborators (9)

Nuno Maia

Ana do Carmo Azevedo

Sara Cavaco

Natália Oliva Teles

Cláudia Santos Silva

Jorge Sequeiros

Esmeralda Neves

Rui Magalhães

João Lemos

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