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"Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia

American journal of neuroradiology : AJNR, 2019-01, Vol.40 (1), p.199-203

2019

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Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems

European journal of neurology, 2009-08, Vol.16 (8), p.887-888

Hedera, P.

2009

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Update on the clinical management of Wilson's disease

Application of clinical genetics, 2017-01, Vol.10, p.9-19

Hedera, Peter

2017

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Novel THAP1 sequence variants in primary dystonia

Neurology, 2010-01, Vol.74 (3), p.229-238

2010

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Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3

Neurology, 2007-06, Vol.68 (24), p.2107-2112

2007

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Deep brain stimulation in early Parkinson’s disease: Enrollment experience from a pilot trial

Parkinsonism & related disorders, 2012-03, Vol.18 (3), p.268-273

2012

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Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy

Journal of neurology, neurosurgery and psychiatry, 2006-02, Vol.77 (2), p.208-215

2006

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Deep brain stimulation therapy of levodopa-responsive motor fluctuations in patients with multiple system atrophy

Parkinsonism & related disorders, 2018-01, Vol.46, p.e91-e91

2018

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Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia

Neuroradiology, 2005-10, Vol.47 (10), p.730-734

2005

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Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3

Neurology, 2007-06, Vol.68 (24), p.2107

2007

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Hyperkinetic psychogenic movement disorders remain a diagnosis at first sight

Neurology, 2017-01, Vol.88 (2), p.114-115

2017

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2.334 EFFICACY OF SUBTHALAMIC NUCLEUS DEEP BRAIN STIMULATION FOR LEG TREMOR CONTROL IN PARKINSON'S DISEASE

Parkinsonism & related disorders, 2012, Vol.18, p.S150-S150

2012

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Can a specific deep brain stimulation paradigm slow motor progression and provide long-term motor benefit in Parkinson’s disease?

Parkinsonism & related disorders, 2024-05, Vol.122, p.106131, Article 106131

2024

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Ethical Principles and Pitfalls of Genetic Testing for Dementia

Journal of geriatric psychiatry and neurology, 2001-12, Vol.14 (4), p.213-221

Hedera, Peter

2001

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Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q

American journal of human genetics, 1999-02, Vol.64 (2), p.563-569

1999

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Identification of vascular structures as a major source of signal contrast in high resolution 2D and 3D functional activation imaging of the motor cortex at l.5T preliminary results

Magnetic resonance in medicine, 1993-09, Vol.30 (3), p.387-392

1993

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Familial genetic predisposition, epilepsy localization and antecedent febrile seizures

Epilepsy research, 2007-01, Vol.73 (1), p.104-110

2007

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Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients

European journal of neurology, 2007-04, Vol.14 (4), p.424-427

2007

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Rotigotine adverse effects affecting patient's sexual partner

Clinical neuropharmacology, 2010-01, Vol.33 (1), p.46-47

Hedera, Peter

2010

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A Prospective, Observational Trial of LINAC-Based Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

International journal of radiation oncology, biology, physics, 2017-10, Vol.99 (2), p.S102-S102

2017

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Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q

American journal of human genetics, 1996-07, Vol.59 (1), p.140-145

1996

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Volumetric magnetic resonance imaging differences in essential tremor compared to Parkinson’s disease

Parkinsonism & related disorders, 2018-01, Vol.46, p.e36-e36

2018

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Stroke risk factors and development of collateral flow in carotid occlusive disease

Acta neurologica Scandinavica, 1998-09, Vol.98 (3), p.182-186

1998

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Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q

Neurology, 1999-07, Vol.53 (1), p.44-44

1999

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"Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia

Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems

Update on the clinical management of Wilson's disease

Novel THAP1 sequence variants in primary dystonia

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3

Deep brain stimulation in early Parkinson’s disease: Enrollment experience from a pilot trial

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy

Deep brain stimulation therapy of levodopa-responsive motor fluctuations in patients with multiple system atrophy

Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3

Hyperkinetic psychogenic movement disorders remain a diagnosis at first sight

Safety and efficacy of abobotulinumtoxinA for hemiparesis in adults with upper limb spasticity after stroke or traumatic brain injury: a double-blind randomised controlled trial

2.334 EFFICACY OF SUBTHALAMIC NUCLEUS DEEP BRAIN STIMULATION FOR LEG TREMOR CONTROL IN PARKINSON'S DISEASE

Can a specific deep brain stimulation paradigm slow motor progression and provide long-term motor benefit in Parkinson’s disease?

Ethical Principles and Pitfalls of Genetic Testing for Dementia

Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q

Identification of vascular structures as a major source of signal contrast in high resolution 2D and 3D functional activation imaging of the motor cortex at l.5T preliminary results

Familial genetic predisposition, epilepsy localization and antecedent febrile seizures

Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients

Rotigotine adverse effects affecting patient's sexual partner

A Prospective, Observational Trial of LINAC-Based Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q

Volumetric magnetic resonance imaging differences in essential tremor compared to Parkinson’s disease

Stroke risk factors and development of collateral flow in carotid occlusive disease

Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q

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