(Q27005740)

10

object named as

Kailash P. Bhatia

1 reference

Annu Aggarwal

3

0 references

Maria Stamelou

1

object named as

Maria Stamelou

1 reference

Scarlett C. Lai

2

1 reference

Susanne A. Schneider

4

1 reference

Tu-Hsueh Yeh

6

1 reference

Amit Batla

7

1 reference

Chin-Song Lu

8

1 reference

Mohit Bhatt

9

1 reference

language of work or name

1 reference

September 2013

1 reference

1 September 2013

5 references

24 March 2019

25 April 2019

7 August 2019

12 September 2019

29 April 2021

6 references

24 March 2019

25 April 2019

7 August 2019

12 September 2019

29 April 2021

28

1 reference

issue

10

1 reference

page(s)

1325-9

1 reference

Creative Commons Attribution 3.0 Unported

copyright license

5 references

24 March 2019

25 April 2019

7 August 2019

12 September 2019

on focus list of Wikimedia project

29 April 2021

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

Neurodegeneration with brain iron accumulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Clinical and genetic delineation of neurodegeneration with brain iron accumulation

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

L-Glutaric acidemia: investigation of a patient and his family

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Tardive dyskinesia is caused by maladaptive synaptic plasticity: a hypothesis

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Therapeutic advances in neurodegeneration with brain iron accumulation.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Syndromes of neurodegeneration with brain iron accumulation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Dopa-responsive dystonia with a novel initiation codon mutation in the GCH1 gene misdiagnosed as cerebral palsy.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Movement disorder emergencies in childhood

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Hallervorden-Spatz disease: historical case presentation in the spotlight of nosological evolution

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Rare causes of dystonia parkinsonism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Dystonia in neurodegeneration with brain iron accumulation: outcome of bilateral pallidal stimulation.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Complicated recessive dystonia parkinsonism syndromes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Delineation of the motor disorder of Lesch-Nyhan disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Misdiagnoses in children with dopa-responsive dystonia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Stereotactic pallidotomy in a child with Hallervorden-Spatz disease. Case report

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Geste device in tardive dystonia with retrocollis and opisthotonic posturing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Clinical features and natural history of axial predominant adult onset primary dystonia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

A case of maple syrup urine disease misdiagnosed as tetanus neonatorum on admission.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Maple syrup urine disease: clinical, EEG, and plasma amino acid correlations with a theoretical mechanism of acute neurotoxicity

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Neuroferritinopathy: update on clinical features and pathogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Neurological manifestations in Wilson's disease: Report of 119 cases.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

The natural history of tardive dystonia. A long-term follow-up study of 107 cases.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Clinico-pathological and histochemical studies of Hallervorden-Spatz disease with torsion dystonia with special reference to diagnostic criteria of the disease from the clinico-pathological viewpoint.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

Natural history and treatment of tardive dystonia.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease.

31 May 2018

1 reference

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

21 January 2018

1 reference

Aromatic L-amino acid decarboxylase deficiency: clinical features, drug therapy and follow-up

21 January 2018

1 reference

"Progressive delayed-onset postanoxic dystonia" diagnosed with PANK2 mutations 26 years after onset-an update

21 January 2018

1 reference

Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients

21 January 2018

1 reference

Markedly severe dystonia in Japanese encephalitis

21 January 2018

1 reference

Arc de cercle and dysautonomia from anoxic injury.

21 January 2018

1 reference

Recurrent opisthotonus in catatonia: An atypical presentation

21 January 2018

1 reference

Pallidal stimulation improves pantothenate kinase-associated neurodegeneration

21 January 2018

1 reference

The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration.

21 January 2018

1 reference

Extensor truncal dystonia: successful treatment with botulinum toxin injections

21 January 2018

1 reference

Neurodegeneration with brain iron accumulation: clinical, radiographic and genetic heterogeneity and corresponding therapeutic options.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

A case of cephalic tetanus presenting with opisthotonus

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4208296

28 November 2018

1 reference

12 December 2020

Idiopathic NBIA--clinical spectrum and transcranial sonography findings

1 reference

12 December 2020

Clinical comparison of tardive and idiopathic cervical dystonia

1 reference

12 December 2020

Intrafamilial phenotypic variability of Hallervorden-Spätz syndrome in a Tunisian family

1 reference

12 December 2020

Bilateral subthalamic nucleus stimulation in the treatment of neurodegeneration with brain iron accumulation type 1

1 reference

12 December 2020

Metabolic encephalopathies

1 reference

12 December 2020

METABOLIC DISORDERS IN HALLERVORDEN-SPATZ DISEASE

1 reference

12 December 2020

Hallervorden-Spatz syndrome

1 reference

12 December 2020

Three faces of the same gene: FA2H links neurodegeneration with brain iron accumulation, leukodystrophies, and hereditary spastic paraplegias

1 reference

12 December 2020

release_cejkn3snlrbaviihaidervb33u

Identifiers

DOI

10.1002/MDS.25490

0 references

Fatcat ID

0 references

1 reference

PubMed publication ID

23736975

1 reference