His primary areas of study are Epilepsy, Pediatrics, Genetics, Encephalopathy and Anesthesia. Epilepsy is a primary field of his research addressed under Psychiatry. The Pediatrics study combines topics in areas such as Central nervous system disease, Status epilepticus, Lennox–Gastaut syndrome, Rufinamide and Disease.
His Genetics research is multidisciplinary, relying on both Corpus Callosum Agenesis and Developmental disorder. His work deals with themes such as Hypotonia, Epileptic spasms and Movement disorders, which intersect with Encephalopathy. His studies in Anesthesia integrate themes in fields like Epilepsy syndromes and Febrile infection related epilepsy syndrome.
Gerhard Kluger focuses on Epilepsy, Pediatrics, Anesthesia, Rufinamide and Psychiatry. His research in Epilepsy intersects with topics in Encephalopathy and Electroencephalography. His studies deal with areas such as Tolerability, Adverse effect, Retrospective cohort study and Dravet syndrome as well as Pediatrics.
Many of his studies involve connections with topics such as Convulsion and Anesthesia. His Rufinamide course of study focuses on Lennox–Gastaut syndrome and Placebo. His research in Status epilepticus is mostly focused on Febrile infection related epilepsy syndrome.
Epilepsy, Pediatrics, Dravet syndrome, Cohort study and SYNGAP1 are his primary areas of study. Gerhard Kluger merges many fields, such as Epilepsy and Outcome, in his writings. He interconnects Epilepsy surgery, Electroencephalography and Topiramate in the investigation of issues within Pediatrics.
His Dravet syndrome research focuses on Quality of life and how it connects with Wakefulness, Activities of daily living and Psychiatry. In his study, Early disease, Clinical research, Tuberous sclerosis and Vigabatrin is inextricably linked to Medical prescription, which falls within the broad field of Cohort study. His SYNGAP1 research includes elements of Young adult, Treatment outcome, Term effect, Reflex and Rosuvastatin.
Gerhard Kluger mainly investigates Epilepsy, Pediatrics, Dravet syndrome, Depression and Indirect costs. The concepts of his Epilepsy study are interwoven with issues in Episodic ataxia, Internal medicine, Cohort study, Cohort and Autism spectrum disorder. In the field of Internal medicine, his study on Acetazolamide overlaps with subjects such as Sleep deprivation.
Many of his studies on Pediatrics involve topics that are commonly interrelated, such as Electroencephalography. Gerhard Kluger has included themes like Hippocampal sclerosis, Temporal lobe, Reflex and Gene mutation in his Electroencephalography study. Gerhard Kluger combines subjects such as Quality of life, Univariate analysis and Encephalopathy with his study of Depression.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology
Alexis Arzimanoglou;Jacqueline French;Warren T. Blume;J. Helen Cross.
Lancet Neurology (2009)
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Johannes R Lemke;Dennis Lal;Eva M Reinthaler;Isabelle Steiner.
Nature Genetics (2013)
Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome
T. Glauser;G. Kluger;R. Sachdeo;G. Krauss.
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff;Katrine M Johannesen;Ulrike B S Hedrich;Silvia Masnada.
Febrile infection-related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children.
Uri Kramer;Ching Shiang Chi;Kuang Lin Lin;Nicola Specchio.
Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood.
Andreas Van Baalen;Martin Häusler;Rainer Boor;Axel Rohr.
The phenotypic spectrum of SCN8A encephalopathy
Jan Larsen;Gemma L Carvill;Elena Gardella;Gerhard Kluger.
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Fanny Kortüm;Soma Das;Max Flindt;Deborah J Morris-Rosendahl.
Journal of Medical Genetics (2011)
Limbic encephalitis in children and adolescents
E Haberlandt;T Bast;A Ebner;H Holthausen.
Archives of Disease in Childhood (2011)
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome
Arvid Suls;Johanna A. Jaehn;Angela Kecskés;Yvonne Weber.
American Journal of Human Genetics (2013)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: