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Ki Wha Chung Selected Research

familial Temporal epilepsy

10/2018A Novel Nonsense Mutation in Leucine-Rich, Glioma-Inactivated-1 Gene as the Underlying Cause of Familial Temporal Lobe Epilepsy.

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Ki Wha Chung Research Topics

Disease

9Charcot-Marie-Tooth Disease (Peroneal Muscular Atrophy)
01/2022 - 01/2008
4Peripheral Nervous System Diseases (PNS Diseases)
01/2022 - 08/2013
3Hereditary Sensory and Motor Neuropathy (Dejerine Sottas Disease)
01/2019 - 06/2014
3Mitochondrial Diseases (Mitochondrial Disease)
10/2015 - 06/2008
2Neurodegenerative Diseases (Neurodegenerative Disease)
04/2022 - 11/2016
2Type 1F Charcot-Marie-Tooth disease
01/2022 - 01/2008
2Type 2D Charcot-Marie-Tooth disease
01/2022 - 12/2012
2Type 2E Charcot-Marie-Tooth disease
01/2022 - 01/2008
2MELAS Syndrome (Syndrome, MELAS)
06/2010 - 06/2008
1Neuromuscular Junction Diseases
04/2022
1Hypoxia (Hypoxemia)
01/2020
1familial Temporal epilepsy
10/2018
1Mitochondrial Encephalomyopathies (Mitochondrial Encephalomyopathy)
01/2017
1Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
01/2017
1Demyelinating Diseases (Demyelinating Disease)
11/2016
1Globoid Cell Leukodystrophy (Krabbe Disease)
11/2016
1Distal Myopathies (Distal Muscular Dystrophy)
02/2016
1Navajo neurohepatopathy
10/2015
1Muscular Diseases (Myopathy)
08/2014
1Ataxia (Dyssynergia)
04/2014
1Deafness (Deaf Mutism)
04/2014
1Myoclonus (Nocturnal Myoclonus)
04/2014
1Hereditary Sensory and Autonomic Neuropathies (HSAN)
02/2014
1Foot Ulcer
02/2014
1Myoglobinuria
12/2013
1Cardiomyopathies (Cardiomyopathy)
12/2013
1Hypoglycemia (Reactive Hypoglycemia)
12/2013
1Neoplasms (Cancer)
01/2013
1Type V Distal Hereditary Motor Neuronopathy
12/2012
1MERRF Syndrome (Myoclonic Epilepsy and Ragged Red Fibers)
06/2010
1Type 2F Charcot-Marie-Tooth disease
06/2008
1Disease Susceptibility (Diathesis)
04/2008
1Squamous Cell Carcinoma (Epidermoid Carcinoma)
05/2007
1Basal Cell Carcinoma (Rodent Ulcer)
05/2007

Drug/Important Bio-Agent (IBA)

4Mitochondrial DNA (mtDNA)IBA
08/2014 - 06/2008
3Small Heat-Shock ProteinsIBA
01/2022 - 06/2008
2Proteins (Proteins, Gene)FDA Link
01/2022 - 12/2013
2Glycine-tRNA LigaseIBA
01/2022 - 12/2012
2GDAP proteinIBA
01/2021 - 01/2008
2periaxinIBA
01/2019 - 01/2015
2Nonsense Codon (Nonsense Mutation)IBA
10/2018 - 01/2017
2EnzymesIBA
11/2016 - 12/2012
1CKD-504IBA
04/2022
1Histone Deacetylase 6IBA
04/2022
1Biomarkers (Surrogate Marker)IBA
01/2022
1Amino Acyl-tRNA Synthetases (Aminoacyl-tRNA Synthetase)IBA
01/2022
1neurofilament protein LIBA
01/2022
1Myelin P0 Protein (Myelin Protein Zero)IBA
01/2021
1TubulinIBA
01/2020
1Vascular Endothelial Growth Factor A (Vascular Endothelial Growth Factor)IBA
01/2020
1Aurora Kinase AIBA
01/2020
1Leucine (L-Leucine)FDA Link
10/2018
13' Untranslated Regions (3' UTR)IBA
01/2017
1Neurofilament ProteinsIBA
01/2017
1Psychosine (Galactosylsphingosine)IBA
11/2016
1GalactosylceramidaseIBA
11/2016
1Creatine Kinase (Creatine Phosphokinase)IBA
02/2016
1DNA (Deoxyribonucleic Acid)IBA
10/2015
1Amino AcidsFDA Link
02/2014
1Serine C-PalmitoyltransferaseIBA
02/2014
1Coenzyme A (CoA)IBA
12/2013
1Oxidoreductases (Dehydrogenase)IBA
12/2013
1Enoyl-CoA HydrataseIBA
12/2013
1Ribose-Phosphate Pyrophosphokinase (Phosphoribosyl Pyrophosphate Synthetase)IBA
10/2013
1Codon (Codons)IBA
08/2013
1alpha-Crystallins (alpha-Crystallin)IBA
08/2013
1Nitric Oxide (Nitrogen Monoxide)FDA Link
01/2013
1Glycine (Aminoacetic Acid)FDA LinkGeneric
12/2012
1Gly Transfer RNAIBA
12/2012
1Leu Transfer RNAIBA
06/2010
1Lys Transfer RNAIBA
06/2010
1NADH DehydrogenaseIBA
06/2008
1Electron Transport Complex IV (Cytochrome c Oxidase)IBA
06/2008
1Genetic Markers (Genetic Marker)IBA
04/2008
1Peptides (Polypeptides)IBA
01/2008
1arginylarginine (Arg-Arg)IBA
05/2007
1tryptophyltryptophanIBA
05/2007
1arginyl-glutamineIBA
05/2007

Therapy/Procedure

1Precision Medicine
06/2014
1Surgical Amputation (Amputations)
02/2014