(Q42970950)

12 November 2017

title

Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms (English)

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12 November 2017

Annu Aggarwal

1

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Monty Silverdale

object named as

Monty Silverdale

4

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John Anthony Hardy

10

object named as

John Hardy

1 reference

Kailash Phatechand Bhatia

12 November 2017

11

object named as

Kailash P Bhatia

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12 November 2017

Susanne A Schneider

2

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12 November 2017

Henry Houlden

3

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12 November 2017

Reema Paudel

5

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12 November 2017

Coro Paisan-Ruiz

6

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12 November 2017

Shrinivas Desai

7

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12 November 2017

Mihir Munshi

8

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12 November 2017

Darshana Sanghvi

9

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12 November 2017

Mohit Bhatt

12

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12 November 2017

language of work or name

English

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publication date

1 July 2010

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12 November 2017

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12 November 2017

volume

25

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12 November 2017

issue

10

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12 November 2017

page(s)

1424-1431

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Complicated recessive dystonia parkinsonism syndromes

12 November 2017

cites work

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Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations

21 January 2018

1 reference

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

21 January 2018

1 reference

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

21 January 2018

1 reference

T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation

21 January 2018

1 reference

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation

21 January 2018

1 reference

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

21 January 2018

1 reference

Severe tongue protrusion dystonia: clinical syndromes and possible treatment.

21 January 2018

1 reference

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

21 January 2018

1 reference

Clinical and genetic delineation of neurodegeneration with brain iron accumulation

21 January 2018

1 reference

Pantothenate kinase associated neurodegeneration (Hallervorden-Spatz syndrome).

21 January 2018

1 reference

Clinical heterogeneity in Hallervorden-Spatz syndrome: a clinicoradiological study in 13 patients from South India

21 January 2018

1 reference

Relaxation and susceptibility MRI characteristics in Hallervorden-Spatz syndrome

21 January 2018

1 reference

Hallervorden-Spatz disease: late infantile type.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.23095

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12 November 2017

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