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@ARTICLE{Miranda:163926,
author = {Miranda, Marcelo and Harmuth, Florian and Bustamante, M
Leonor and Rossi, Malco and Sturm, Marc and Magnusson,
Ólafur Th and Bauer, Peter and Klockgether, Thomas and
Ramirez, Alfredo},
title = {{I}ntermediate phenotype of {ATP}13{A}2 mutation in two
{C}hilean siblings: {T}owards a continuum between
parkinsonism and hereditary spastic paraplegia.},
journal = {Parkinsonism $\&$ related disorders},
volume = {81},
issn = {1353-8020},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {DZNE-2022-00603},
pages = {45 - 47},
year = {2020},
subtyp = {Letter},
keywords = {Adolescent / Ataxia: physiopathology / Cognitive
Dysfunction: physiopathology / Cognitive Dysfunction:
psychology / Female / Humans / Male / Motor Neuron Disease:
physiopathology / Muscle Spasticity: physiopathology /
Ocular Motility Disorders: physiopathology / Parkinsonian
Disorders: genetics / Parkinsonian Disorders:
physiopathology / Parkinsonian Disorders: psychology /
Phenotype / Proton-Translocating ATPases: genetics /
Psychotic Disorders: physiopathology / Psychotic Disorders:
psychology / Siblings / Spastic Paraplegia, Hereditary:
genetics / Spastic Paraplegia, Hereditary: physiopathology /
Spastic Paraplegia, Hereditary: psychology / Young Adult /
ATP13A2 (Other) / Kufor-Rakeb syndrome (Other) /
Parkinsonism (Other) / SPG78 (Other) / Spastic paraplegia
(Other) / ATP13A2 protein, human (NLM Chemicals) /
Proton-Translocating ATPases (NLM Chemicals)},
cin = {Patient Studies Bonn / AG Klockgether},
ddc = {610},
cid = {I:(DE-2719)1011101 / I:(DE-2719)1011001},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:33049588},
doi = {10.1016/j.parkreldis.2020.10.004},
url = {https://pub.dzne.de/record/163926},
}