Jürgen Sperner

Medicine · Health Sciences

23h-index2.7kcitations86works0.02yr avg
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Research Topics

Neurological disorders and treatments(15), Epilepsy research and treatment(10), Metabolism and Genetic Disorders(9), Vagus Nerve Stimulation Research(9), Mitochondrial Function and Pathology(8)

Publications86 total

Methylphenidate Can Improve Chorea in <i>NKX2.1</i> and <i>ADCY5</i> Mutation‐positive Patients—A Report of Two Children
Movement Disorders Clinical Practice·2018· 18 citedOpen Access
Terrestrial laser scanning for heritage conservation:the Cologne Cathedral documentation project
ISPRS annals of the photogrammetry, remote sensing and spatial information sciences·2017· 60 citedOpen Access
Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases
The Journal of Pediatrics·2016· 29 cited
Desmoplastic Infantile Ganglioglioma
Elsevier eBooks·2016· 6 cited
Paroxysmal hemichorea after streptococcal infection-clinical and diagnostic findings
Journal of Pediatric Neurology·2015
Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
Epilepsy Research·2015· 6 cited
Transcranial direct current stimulation for refractory epilepsy in children
Neurophysiologie Clinique·2013
O93 – 2003 Different aspects in the evaluation of vagus nerve stimulation efficacy among children with therapy-refractory epilepsy
European Journal of Paediatric Neurology·2013
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Nature Genetics·2013· 436 cited
Microdeletion 5q14.3 and anomalies of brain development
American Journal of Medical Genetics Part A·2013· 50 cited
A De Novo Mutation in the β-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
The American Journal of Human Genetics·2013· 192 citedOpen Access
Beneficial Prenatal Levodopa Therapy in Autosomal Recessive Guanosine Triphosphate Cyclohydrolase 1 Deficiency
Archives of Neurology·2012· 34 cited
Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?
Neuropediatrics·2012
Bowel Obstruction in Patients with Alpers-Huttenlocher Syndrome
Neuropediatrics·2011· 13 cited
S1.4 Transcranial direct current stimulation for treatment-refractory epilepsy in children: a pilot study
Clinical Neurophysiology·2011
1FC1.1 Transcranial direct current stimulation for treatment-refractory epilepsy in children: A pilot study
European Journal of Paediatric Neurology·2011
Cerebral hemiatrophy associated with hippocampal sclerosis following a single prolonged febrile seizure
European Journal of Pediatrics·2011· 3 cited
Operative and Technical Complications of Vagus Nerve Stimulator Implantation
Operative Neurosurgery·2010· 102 cited
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Neuropediatrics·2010
Deletions in 16p13 including <i>GRIN2A</i> in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region
Epilepsia·2010· 99 cited
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Frequent Co-authors

Christine Klein(6), D. Scheffner(5), Christoph Härtel(5), Rainer Boor(4), Ulrich Stephani(4), Gabriele Gillessen‐Kaesbach(4), Juliane Spiegler(4), Norman Kock(3), Sebastian Spuck(3), Ute Thyen(3), Hans Henkes(3), C. Bassir(3), Yorck Hellenbroich(3), Norbert Brüggemann(3), Alexander Münchau(3), Stefan Schilling(3), Katrin Finsterwalder(2), Hiltrud Muhle(2), Sarah Weckhuysen(2), Gerhard Kurlemann(2)