Diagnosis across a cohort of “atypical” atypical and complex parkinsonism
Maria João Malaquias(Administração Regional de Saúde de Lisboa e Vale do Tejo), Marina Magalhães(Centro Hospitalar Lisboa Norte), Célia Nogueira(National Institute of Health Dr. Ricardo Jorge), Laura Vilarinho(National Institute of Health Dr. Ricardo Jorge), Jorge Oliveira(Centro Hospitalar Lisboa Norte), Liliana Igreja(RCA (United States)), Dulce Quelhas, João Parente Freixo(i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto), Cristina Pereira(National Institute of Health Dr. Ricardo Jorge)
Cited by 3
Related Papers
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement
|The American Journal of Human Genetics|2022|22
Multisystemic <i>RFC1</i> -Related Disorder
|Neurology Clinical Practice|2023|21
Acquired hepatocerebral degeneration and hepatic encephalopathy: one or two entities?
|European Journal of Neurology|2020|20
Diagnosis of Aicardi‐Goutières Syndrome in Adults: A Case Series
|Movement Disorders Clinical Practice|2020|18
GNAO1 mutation presenting as dyskinetic cerebral palsy
|Neurological Sciences|2019|17