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methionine and Familial Spastic Paraparesis, Htlv-1-Associated

methionine has been researched along with Familial Spastic Paraparesis, Htlv-1-Associated in 1 studies

Research

Studies (1)

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

Authors

Authors	Studies
Cooper, BA; Dilling, LA; Haworth, JC; Lue-Shing, H; Rosenblatt, DS; Seargeant, LE; Surtees, RA	1

Other Studies

1 other study(ies) available for methionine and Familial Spastic Paraparesis, Htlv-1-Associated

Article	Year
Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers. American journal of medical genetics, 1993, Mar-01, Volume: 45, Issue:5 Topics: Adult; Betaine; Enzyme Stability; Folic Acid; Homocystine; Humans; Male; Metabolism, Inborn Errors; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Nervous System Diseases; Oxidoreductases Acting on CH-NH Group Donors; Paraparesis, Tropical Spastic	1993

Article

Year

Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers.

American journal of medical genetics, 1993, Mar-01, Volume: 45, Issue:5

Topics: Adult; Betaine; Enzyme Stability; Folic Acid; Homocystine; Humans; Male; Metabolism, Inborn Errors; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Nervous System Diseases; Oxidoreductases Acting on CH-NH Group Donors; Paraparesis, Tropical Spastic

1993