Page last updated: 2024-08-23

s-adenosylmethionine and Retinitis Pigmentosa

s-adenosylmethionine has been researched along with Retinitis Pigmentosa in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chang, YS; Jin, DK; Ki, CS; Kim, SR; Lee, SY; Park, HD; Park, WS	1

Other Studies

1 other study(ies) available for s-adenosylmethionine and Retinitis Pigmentosa

Article	Year
Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency. Annals of clinical and laboratory science, 2009,Fall, Volume: 39, Issue:4 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Myopathies; Mitochondrial Proteins; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Republic of Korea; Retinitis Pigmentosa; Rhabdomyolysis	2009

Article

Year

Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.

Annals of clinical and laboratory science, 2009,Fall, Volume: 39, Issue:4

Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Myopathies; Mitochondrial Proteins; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Republic of Korea; Retinitis Pigmentosa; Rhabdomyolysis

2009