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CEREBELLAR ATAXIA
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CEREBELLAR ATAXIA
CAPN1
mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype
Jeffrey
Lambe
,
Bernadette
Monaghan
,
Tudor
Munteanu
,
Janice
Redmond
Practical Neurology
Apr 2018,
practneurol-2017-001842;
DOI:
10.1136/practneurol-2017-001842
Gordon Holmes syndrome: finally genotype meets phenotype
Shahid
Mehmood
,
Nigel
Hoggard
,
Marios
Hadjivassiliou
Practical Neurology
Dec 2017,
17
(6)
476-478;
DOI:
10.1136/practneurol-2017-001674
Hypothyroid ataxia complicating monoclonal antibody therapy
Abdul
Badran
,
Carla
Moran
,
Alasdair J
Coles
Practical Neurology
Dec 2017,
17
(6)
482-484;
DOI:
10.1136/practneurol-2017-001713
A taxing case
David
Bourke
,
Laurie
Wing
Practical Neurology
Oct 2016,
16
(5)
394-397;
DOI:
10.1136/practneurol-2015-001177
A case of cystinuria presenting with cerebellar ataxia and dementia
Rie
Tohge
,
Shinichi
Sakamoto
,
Makio
Takahashi
Practical Neurology
Aug 2016,
16
(4)
296-299;
DOI:
10.1136/practneurol-2016-001374
Acute cerebellar syndrome associated with metronidazole
F
Ward
,
P
Crowley
,
P E
Cotter
Practical Neurology
Aug 2015,
15
(4)
298-299;
DOI:
10.1136/practneurol-2014-000974
Niemann–Pick type C: a potentially treatable disorder?
Ammar
Kheder
,
Camilla
Scott
,
Simon
Olpin
,
Marios
Hadjivassiliou
Practical Neurology
Dec 2013,
13
(6)
382-385;
DOI:
10.1136/practneurol-2013-000525
CLINICAL
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(8)
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(61)
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(10)
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(66)
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(197)
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(28)
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(6)
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(2)
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(26)
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(3)
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(4)
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(1)
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(26)
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(11)
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(36)
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(63)
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(1)
