HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Masakazu Kohda Selected Research

Leigh Disease (Leigh's Disease)

12/2021Valine metabolites analysis in ECHS1 deficiency.
11/2020Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL.
1/2020Mortality of Japanese patients with Leigh syndrome: Effects of age at onset and genetic diagnosis.
1/2019Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.
12/2014Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.
5/2014New MT-ND6 and NDUFA1 mutations in mitochondrial respiratory chain disorders.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Masakazu Kohda Research Topics

Disease

10Mitochondrial Diseases (Mitochondrial Disease)
11/2021 - 02/2015
6Leigh Disease (Leigh's Disease)
12/2021 - 05/2014
3Cardiomyopathies (Cardiomyopathy)
03/2019 - 03/2016
2Chromosome Aberrations (Chromosome Abnormalities)
10/2021 - 01/2016
2Neoplasms (Cancer)
02/2016 - 04/2010
2Diabetic Retinopathy (Retinopathy, Diabetic)
01/2015 - 01/2014
1Dystonia (Limb Dystonia)
12/2021
1Mitochondrial complex I deficiency
11/2021
1Lactic Acidosis
11/2020
1Brain Diseases (Brain Disorder)
10/2020
1Trichohepatoenteric Syndrome
04/2020
1Cardiac Arrhythmias (Arrythmia)
04/2020
1Bloom Syndrome
01/2018
1Genomic Instability
01/2018
1Infections
10/2017
1Inflammation (Inflammations)
10/2017
1Type C Niemann-Pick Disease (Niemann Pick Disease, Type C)
06/2017
1Cerebellar Diseases (Cerebellar Syndrome)
06/2017
1Neurodegenerative Diseases (Neurodegenerative Disease)
06/2017
1Dilated Cardiomyopathy (Cardiomyopathy, Congestive)
04/2017
1Hereditary Nonpolyposis Colorectal Neoplasms (Hereditary Nonpolyposis Colorectal Cancer)
02/2016
1Colonic Neoplasms (Colon Cancer)
02/2016
1Mesothelioma
04/2010
1Malignant Mesothelioma
04/2010
1Myositis Ossificans (Fibrodysplasia Ossificans Progressiva)
03/2009
1Breast Neoplasms (Breast Cancer)
11/2007

Drug/Important Bio-Agent (IBA)

7Proteins (Proteins, Gene)FDA Link
11/2020 - 04/2010
6Mitochondrial DNA (mtDNA)IBA
11/2021 - 01/2016
3DNA (Deoxyribonucleic Acid)IBA
11/2021 - 11/2007
2EnzymesIBA
11/2020 - 05/2014
2OligonucleotidesIBA
12/2017 - 01/2016
2Pharmaceutical PreparationsIBA
06/2017 - 04/2010
2coenzyme Q10 (CoQ10)IBA
11/2015 - 02/2015
2Untranslated RNA (Noncoding RNA)IBA
01/2015 - 01/2014
1Amino AcidsFDA Link
12/2021
1Enoyl-CoA HydrataseIBA
12/2021
1Fatty Acids (Saturated Fatty Acids)IBA
12/2021
1RNA (Ribonucleic Acid)IBA
11/2021
1Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate ElevationIBA
11/2020
1Triglycerides (Triacylglycerol)IBA
04/2020
1Indicators and Reagents (Reagents)IBA
03/2019
1Ribosomal Proteins (Ribosomal Protein)IBA
01/2019
1CholesterolIBA
06/2017
1C 39 (C39)IBA
04/2017
1oligomycin sensitivity-conferring protein (complex V)IBA
03/2016
1Adenosine Triphosphatases (ATPase)IBA
03/2016
1MutS ProteinsIBA
02/2016
1Epithelial Cell Adhesion MoleculeIBA
02/2016
1Mitochondrial Proteins (Mitochondrial Protein)IBA
01/2016
1Thioctic Acid (Lipoic Acid)IBA
11/2015
1AsbestosIBA
04/2010
1Small Interfering RNA (siRNA)IBA
04/2010
1Bone Morphogenetic Proteins (Bone Morphogenetic Protein)IBA
03/2009

Therapy/Procedure

1Therapeutics
01/2020
1Radiotherapy
11/2007