Neurodegeneration with brain iron accumulation: Characterization of clinical, radiological, and genetic features of pediatric patients from Southern India-Reference-Cited by-同舟云学术

Neurodegeneration with brain iron accumulation: Characterization of clinical, radiological, and genetic features of pediatric patients from Southern India

Published:2021-11 Issue:10 Volume:43 Page:1013-1022
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Bhardwaj Naveen Kumar,Gowda Vykuntaraju K.,Saini Jitendra,Sardesai Ashwin Vivek,Santhoshkumar Rashmi,Mahadevan Anita

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference33 articles.

1. Neurodegeneration with brain iron accumulation;Hayflick;Handb Clin Neurol,2018

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

3. Neurodegeneration with Brain Iron Accumulation Disorders Overview. 2013 [updated 2019];Gregory,1993

4. Clinical and Imaging Presentation of a Patient with Beta-Propeller Protein-Associated Neurodegeneration, a Rare and Sporadic form of Neurodegeneration with Brain Iron Accumulation (NBIA);Hattingen;Clin Neuroradiol,2017

5. Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms;Aggarwal;Mov Disord,2010

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