Juvenile PLA2G6-Parkinsonism Due to Indian 'Asian' p.R741Q Mutation, and Response to STN DBS.

Ravat, Parthvi; Shinde, Swati; Shinde, Shilpa R; Bangar, Santosh; Nayak, Naren; Agarwal, Pankaj A

Ravat, Parthvi; Shinde, Swati; Shinde, Shilpa R; Bangar, Santosh; Nayak, Naren; Agarwal, Pankaj A.

Afiliação

Ravat P; Department of Neurology, Seth GS Medical College and KEM Hospital, Mumbai, India.
Shinde S; Movement Disorders Clinic, Department of Neurology, Global Hospitals Parel, Mumbai, India.
Shinde SR; Department of Neurology, Global Hospitals, Parel, Mumbai, India.
Bangar S; Movement Disorders Clinic, Department of Neurology, Global Hospitals Parel, Mumbai, India.
Nayak N; Department of Neurology, Global Hospitals, Parel, Mumbai, India.
Agarwal PA; Movement Disorders Clinic, Department of Neurology, Global Hospitals Parel, Mumbai, India.

Mov Disord ; 37(3): 657-658, 2022 03.

Article em En | MEDLINE | ID: mdl-35113461

Assuntos

Transtornos Parkinsonianos; Povo Asiático; Fosfolipases A2 do Grupo VI/genética; Humanos; Mutação/genética; Transtornos Parkinsonianos/genética; Transtornos Parkinsonianos/terapia

Palavras-chave

DBS; Indian; PLA2G6; parkinsonism; young-onset parkinsonism

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Parkinsonianos Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google