Difficult and recurrent meningitis

L Ginsberg - Journal of Neurology, Neurosurgery & Psychiatry, 2004 - jnnp.bmj.com
Clinical diagnosis—The classical symptoms and signs of acute meningitis may be absent in
the very young, the very old and the very sick. Chronic meningitis requires a degree of …

[HTML][HTML] POEMS syndrome: clinical update

R Brown, L Ginsberg - Journal of neurology, 2019 - Springer
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin
changes) is a rare paraneoplastic syndrome, caused by a plasma cell proliferative disorder …

Chronic and recurrent meningitis

L Ginsberg, D Kidd - Practical neurology, 2008 - pn.bmj.com
Chronic meningitis is defined as the persistence of clinical symptoms and signs of
meningitis, with or without abnormal cerebrospinal fluid, for more than four weeks. In as …

Disease and anatomic specificity of ethanolamine plasmalogen deficiency in Alzheimer's disease brain

L Ginsberg, S Rafique, JH Xuereb, SI Rapoport… - Brain research, 1995 - Elsevier
A significant and selective deficiency of ethanolamine plasmalogen (PPE) relative to
phosphatidylethanolamine was identified in post mortem brain samples from patients with …

CNS manifestations of Fabry's disease

A Fellgiebel, MJ Müller, L Ginsberg - The Lancet Neurology, 2006 - thelancet.com
Background Fabry's disease is a rare hereditary lysosomal storage disease with multiorgan
involvement. Deficiency of α-galactosidase A activity leads to accumulation of neutral …

Coexistent hereditary and inflammatory neuropathy

L Ginsberg, O Malik, AR Kenton, D Sharp, JR Muddle… - Brain, 2004 - academic.oup.com
Classically, the course of Charcot–Marie–Tooth (CMT) disease is gradually progressive. We
describe eight atypical patients who developed acute or subacute deterioration. Seven of …

A novel RAB7 mutation associated with ulcero‐mutilating neuropathy

H Houlden, RHM King, JR Muddle… - Annals of Neurology …, 2004 - Wiley Online Library
There are two known autosomal dominant genes for the hereditary ulcero‐mutilating
neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot–Marie …

The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

H Houlden, M Laura, L Ginsberg, H Jungbluth… - Neuromuscular …, 2009 - Elsevier
Charcot–Marie–Tooth (CMT) disease is a heterogeneous group of inherited peripheral
motor and sensory neuropathies. The locus responsible for CMT4C was previously …

Neurologic manifestations of the cryopyrin-associated periodic syndrome

JL Kitley, HJ Lachmann, A Pinto, L Ginsberg - Neurology, 2010 - AAN Enterprises
Background: The cryopyrin-associated periodic syndrome (CAPS) is a rare but treatable
hereditary autoinflammatory condition. Without treatment, one third of patients develop …

A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

PA Wilkinson, AH Crosby, C Turner, LJ Bradley… - Brain, 2004 - academic.oup.com
Mutations in the SPG7 gene, encoding the mitochondrial protein paraplegin, were the first to
be identified in autosomal recessive hereditary spastic paraplegia (ARHSP). Four different …