Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life (Q28203623)

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

27 September 2022

N. Nardocci

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

27 September 2022

V. Rumi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

27 September 2022

C. Zorzi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

27 September 2022

L. Strada

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

27 September 2022

M. Savoiardo

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1447570

Progressive dystonia with bilateral putaminal hypodensities

27 September 2022

language of work or name

English

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publication date

October 1992

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published in

Journal of Neurology

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volume

239

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page(s)

417-25

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issue

8

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cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Computed tomography in Hallervorden-Spatz disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Parkinson plus syndrome: diagnosis using high field MR imaging of brain iron.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Clinical NMR imaging of the brain in children: normal and neurologic disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Adult GM1-gangliosidosis: clinical patterns and rectal biopsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Multiple system atrophy (Shy-Drager syndrome): MR imaging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Magnetic resonance imaging in pathologically proven Hallervorden-Spatz disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Sea-blue histiocytes, lymphocytic cytosomes, movement disorder and 59Fe-uptake in basal ganglia: Hallervorden-Spatz disease or ceroid storage disease with abnormal isotope scan?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00856805

Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosis.

21 January 2018

1 reference

12 December 2020

MR imaging in progressive supranuclear palsy and Shy-Drager syndrome

1 reference

12 December 2020

Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features

1 reference

12 December 2020

Hallervorden-Spatz disease: cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus

1 reference

12 December 2020

Computed tomography in Hallervorden-Spatz disease

1 reference

12 December 2020

Pigmentary Degeneration of the Retina in the Hallervorden-Spatz Syndrome

1 reference

12 December 2020

Neuroaxonal dystrophy in childhood. Report of two second cousins with Hallerworden-Spatz disease, and a case of Seitelberger's disease

1 reference

12 December 2020

Hallervorden-Spatz disease and dystonia

1 reference

12 December 2020

Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Ultrastructural observations, anatomical pathology and nosology.

1 reference

12 December 2020

Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations

1 reference

12 December 2020

New computed tomography scan finding in Hallervorden-Spatz syndrome.

1 reference

12 December 2020

MR imaging of Hallervorden-Spatz disease.

1 reference

12 December 2020

The juvenile and chronic forms of GM2 gangliosidosis: clinical and enzymatic heterogeneity.

1 reference

12 December 2020

Hallervorden-Spatz disease.

1 reference

12 December 2020

'Subcortical dementia': the neuropsychological evidence

1 reference

12 December 2020

Idiopathic dystonia with onset in childhood

1 reference

12 December 2020

Hallervorden-Spatz syndrome

1 reference

12 December 2020

MR imaging in a case of Hallervorden-Spatz disease

1 reference

12 December 2020

Early infantile familial forms of pigmentary pallido-reticular atrophy. Critical study of the value of histopathologic criteria in the differentiation of an infantile form of Hallervorden-Spatz disease

1 reference

12 December 2020

Follow-up MR studies in Hallervorden-Spatz disease

1 reference

12 December 2020

Hallervorden-Spatz syndrome

1 reference

12 December 2020

Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy

1 reference

12 December 2020

Dimensions Publication ID

Identifiers

DOI

10.1007/BF00856805

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1036772267

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