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Atypical Bickerstaff brainstem encephalitis: ataxic hypersomnolence without ophthalmoplegia

Journal of neurology, neurosurgery and psychiatry, 2013-11, Vol.84 (11), p.1206-1207

2013

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A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability

Journal of neurology, neurosurgery and psychiatry, 2016-06, Vol.87 (6), p.656-662

2016

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Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (9), p.1024-1028

2014

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Late-onset Boucher–Neuhäuser Syndrome (late BNS) associated with white-matter changes: a report of two cases and review of literature

Journal of neurology, neurosurgery and psychiatry, 2011-08, Vol.82 (8), p.888-891

2011

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Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10)

BMJ case reports, 2022-03, Vol.15 (3), p.e248228

2022

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Gordon Holmes syndrome: finally genotype meets phenotype

Practical neurology, 2017-12, Vol.17 (6), p.476-478

2017

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Selective loss of Purkinje cells in a patient with anti-glutamic acid decarboxylase antibody-associated cerebellar ataxia

Journal of neurology, neurosurgery and psychiatry, 2007-02, Vol.78 (2), p.190-192

2007

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Sniffing out the cerebellum

Journal of neurology, neurosurgery and psychiatry, 2012-10, Vol.83 (10), p.952-953

Houlden, Henry

2012

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Acute cerebellar ataxia and peripheral neuropathy due to an atypical infection

BMJ case reports, 2021-03, Vol.14 (3), p.e242229

2021

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Population based study of late onset cerebellar ataxia in south east Wales

Journal of neurology, neurosurgery and psychiatry, 2004-08, Vol.75 (8), p.1129-1134

2004

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Acute cerebellar ataxia in childhood: initial approach in the emergency department

Emergency medicine journal : EMJ, 2010-12, Vol.27 (12), p.956-957

2010

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Posterior fossa progressive multifocal leukoencephalopathy: first presentation of an unknown autoimmune disease

BMJ case reports, 2017-10, Vol.2017, p.bcr-2017-220990

2017

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Epilepsy and cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies

Journal of neurology, neurosurgery and psychiatry, 2007-02, Vol.78 (2), p.187-189

2007

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Cerebellitis in a human T-lymphotropic virus type 1 carrier: a case report

BMJ case reports, 2021-06, Vol.14 (6), p.e241366

2021

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Autosomal recessive cerebellar ataxias: the current state of affairs

Journal of Medical Genetics, 2011-10, Vol.48 (10), p.651-659

2011

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Cerebellar ataxia and epilepsy with anti-GAD antibodies: treatment with IVIG and plasmapheresis

BMJ case reports, 2014-01, Vol.2014, p.bcr2013202314

2014

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A new dominantly inherited pure cerebellar ataxia, SCA 30

Journal of neurology, neurosurgery and psychiatry, 2009-04, Vol.80 (4), p.408-411

2009

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Neurosyphilis presenting as pure cerebellar ataxia: an atypical manifestation

BMJ case reports, 2019-08, Vol.12 (8), p.e231058

2019

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New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (9), p.968-972

2010

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A case of cystinuria presenting with cerebellar ataxia and dementia

Practical neurology, 2016-08, Vol.16 (4), p.296-299

2016

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Visuospatial abilities in cerebellar disorders

Journal of neurology, neurosurgery and psychiatry, 2004-02, Vol.75 (2), p.235-240

2004

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Hypothyroid ataxia complicating monoclonal antibody therapy

Practical neurology, 2017-12, Vol.17 (6), p.482-484

2017

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Cerebellar ataxia a unique initial presentation of Legionnaires’ disease

BMJ case reports, 2020-03, Vol.13 (3), p.e230710

2020

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Hyponatraemia presenting as reversible cerebellar ataxia in Addison’s disease

BMJ case reports, 2019-08, Vol.12 (8), p.e227933

2019

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Reversible cerebellar toxicity during treatment with ornidazole: the first case report

Journal of neurology, neurosurgery and psychiatry, 2010-03, Vol.81 (3), p.349-350

2010

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Atypical Bickerstaff brainstem encephalitis: ataxic hypersomnolence without ophthalmoplegia

A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

Late-onset Boucher–Neuhäuser Syndrome (late BNS) associated with white-matter changes: a report of two cases and review of literature

Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10)

Gordon Holmes syndrome: finally genotype meets phenotype

Selective loss of Purkinje cells in a patient with anti-glutamic acid decarboxylase antibody-associated cerebellar ataxia

Sniffing out the cerebellum

Acute cerebellar ataxia and peripheral neuropathy due to an atypical infection

Population based study of late onset cerebellar ataxia in south east Wales

Acute cerebellar ataxia in childhood: initial approach in the emergency department

Posterior fossa progressive multifocal leukoencephalopathy: first presentation of an unknown autoimmune disease

Epilepsy and cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies

Cerebellitis in a human T-lymphotropic virus type 1 carrier: a case report

Autosomal recessive cerebellar ataxias: the current state of affairs

Cerebellar ataxia and epilepsy with anti-GAD antibodies: treatment with IVIG and plasmapheresis

A new dominantly inherited pure cerebellar ataxia, SCA 30

Neurosyphilis presenting as pure cerebellar ataxia: an atypical manifestation

New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype

A case of cystinuria presenting with cerebellar ataxia and dementia

Visuospatial abilities in cerebellar disorders

Hypothyroid ataxia complicating monoclonal antibody therapy

Cerebellar ataxia a unique initial presentation of Legionnaires’ disease

Hyponatraemia presenting as reversible cerebellar ataxia in Addison’s disease

Reversible cerebellar toxicity during treatment with ornidazole: the first case report

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