Clinical, imaging and genetic profile of twenty-four patients with pantothenate kinase-associated neurodegeneration (PKAN)- A single centre study from India-Reference-Cited by-同舟云学术

Clinical, imaging and genetic profile of twenty-four patients with pantothenate kinase-associated neurodegeneration (PKAN)- A single centre study from India

Published:2023-06 Issue: Volume:111 Page:105409
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Sriram Neeharika,Holla Vikram V.,Kumari Riyanka,Kamble Nitish,Saini Jitender,Mahale Rohan,Netravathi Manjunath,Padmanabha Hansashree^ORCID,Gowda Vykuntaraju K.^ORCID,Battu Rajani,Pandey Akhilesh,Yadav Ravi,Muthusamy Babylakshmi^ORCID,Pal Pramod Kumar^ORCID

Funder

Department of Health Research, India

Indian Council of Medical Research

Council of Scientific and Industrial Research, India

Ministry of Science and Technology, Pakistan

Ministry of Health and Family Welfare

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference37 articles.

1. Neurodegeneration with brain iron accumulation: diagnosis and management;Hogarth;J Mov Disord,2015

2. Genetic, clinical, and radiographic delineation of Hallervorden–Spatz syndrome;Hayflick;N. Engl. J. Med.,2003

3. Neurodegeneration with brain iron accumulation: characterization of clinical, radiological, and genetic features of pediatric patients from Southern India;Bhardwaj;Brain Dev.,2021

4. A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - India;Angural;Sci. Rep.,2017

5. Magnetic resonance imaging in pantothenate kinase-2-associated neurodegeneration;Singh;J. Pediatr. Neurosci.,2012

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