List of works - Manju A Kurian - Paulina

List of works by Manju A Kurian

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

scientific article published on 17 August 2016

Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.

scientific article

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

scientific article

Phenotypes, genotypes, and the management of paroxysmal movement disorders

scientific article published on 30 March 2018

The expanding spectrum of movement disorders in genetic epilepsies

scientific article published on 29 November 2019

β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation

scientific article published on 17 May 2013

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