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The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity

Neurology, 2006-08, Vol.67 (3), p.430-434

2006

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Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

Journal of neurology, neurosurgery and psychiatry, 2009-12, Vol.80 (12), p.1402-1404

2009

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Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

Clinical genetics, 2011-08, Vol.80 (2), p.148-160

2011

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High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

Neurology, 2006-12, Vol.67 (11), p.1926-1930

2006

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Disease severity affects quality of life of hereditary spastic paraplegia patients

European journal of neurology, 2012-01, Vol.19 (1), p.168-171

2012

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SPG10 is a rare cause of spastic paraplegia in European families

Journal of neurology, neurosurgery and psychiatry, 2008-05, Vol.79 (5), p.584-587

2008

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136. “Compliant 2006” – The value of valproate granules in the therapy of patients with epilepsy: An observational study in 272 patients

Clinical neurophysiology, 2009, Vol.120 (1), p.e56-e57

2009

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Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24

Neurology, 2009-06, Vol.72 (22), p.1893-1898

2009

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Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

Human mutation, 2002-08, Vol.20 (2), p.127-132

2002

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Evaluating the effect of spastin splice mutations by quantitative allele-specific expression assay

European journal of neurology, 2011-01, Vol.18 (1), p.99-105

2011

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Recruitment of motor cortical excitability in untreated patients with epilepsy

Clinical neurophysiology, 2007-04, Vol.118 (4), p.e59-e59

2007

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Are spacial extension and recruitment of motor cortical inhibition related? Evidence using transcranial magnetic stimulation

Clinical neurophysiology, 2007-04, Vol.118 (4), p.e19-e19

2007

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Analysis of correlation between the recruitment of excitation and inhibition in the motor cortex

Clinical neurophysiology, 2007-04, Vol.118 (4), p.e14-e15

2007

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Hemicraniectomy in Older Patients with Extensive Middle-Cerebral-Artery Stroke

The New England journal of medicine, 2014-03, Vol.370 (12), p.1091-1100

2014

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115. Health-related quality of life decreases with disease severity in German HSP patients

Clinical neurophysiology, 2009, Vol.120 (1), p.e48-e49

2009

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Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene

Journal of neurology, neurosurgery and psychiatry, 2003-08, Vol.74 (8), p.1109-1112

2003

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Pregnancy-linked endotheliopathy. A disease with multiple variants?

Nervenarzt, 2012-04, Vol.83 (4), p.510-513

2012

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Early treatment with aspirin plus extended-release dipyridamole for transient ischaemic attack or ischaemic stroke within 24 h of symptom onset (EARLY trial): a randomised, open-label, blinded-endpoint trial

Lancet neurology, 2010-02, Vol.9 (2), p.159-166

2010

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DESTINY II: DEcompressive Surgery for the Treatment of malignant INfarction of the middle cerebral arterY II

International journal of stroke, 2011-02, Vol.6 (1), p.79-86

2011

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Analysis of 100 HSP Exomes and Characterization of Mutations in Known Autosomal Dominant Genes (P05.166)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P05-P05.166

2012

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Antiepileptic drug use in nursing home residents: A cross-sectional, regional study

Seizure (London, England), 2006-04, Vol.15 (3), p.194-197

2006

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Does the recruitment of excitation and inhibition in the motor cortex differ?

Journal of clinical neurophysiology, 2007-10, Vol.24 (5), p.419-423

2007

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Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients: EXOME SEQUENCING

Clinical genetics, 2011, Vol.80 (2), p.148-160

2011

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Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

Neurogenetics, 2004-12, Vol.5 (4), p.239-243

2004

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C6 Syndrom bei Vertebralisdissektion mit V. a. arterio-venöse Fistel: Wurzelkompression oder venöse Stauung?

Klinische Neurophysiologie, 2014, Vol.45 (1)

2014

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The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

Disease severity affects quality of life of hereditary spastic paraplegia patients

SPG10 is a rare cause of spastic paraplegia in European families

136. “Compliant 2006” – The value of valproate granules in the therapy of patients with epilepsy: An observational study in 272 patients

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

Evaluating the effect of spastin splice mutations by quantitative allele-specific expression assay

Recruitment of motor cortical excitability in untreated patients with epilepsy

Are spacial extension and recruitment of motor cortical inhibition related? Evidence using transcranial magnetic stimulation

Analysis of correlation between the recruitment of excitation and inhibition in the motor cortex

Hemicraniectomy in Older Patients with Extensive Middle-Cerebral-Artery Stroke

115. Health-related quality of life decreases with disease severity in German HSP patients

Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene

Pregnancy-linked endotheliopathy. A disease with multiple variants?

Early treatment with aspirin plus extended-release dipyridamole for transient ischaemic attack or ischaemic stroke within 24 h of symptom onset (EARLY trial): a randomised, open-label, blinded-endpoint trial

DESTINY II: DEcompressive Surgery for the Treatment of malignant INfarction of the middle cerebral arterY II

Analysis of 100 HSP Exomes and Characterization of Mutations in Known Autosomal Dominant Genes (P05.166)

Antiepileptic drug use in nursing home residents: A cross-sectional, regional study

Does the recruitment of excitation and inhibition in the motor cortex differ?

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients: EXOME SEQUENCING

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

C6 Syndrom bei Vertebralisdissektion mit V. a. arterio-venöse Fistel: Wurzelkompression oder venöse Stauung?

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