Page last updated: 2024-08-17

methionine and Genetic Diseases

methionine has been researched along with Genetic Diseases in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Elliott, CL; Tabrizi, SJ; Weissmann, C	1
Allen, RH; Baric, I; Cuk, M; Finkelstein, JD; Fumic, K; Glenn, B; James, SJ; Mejaski-Bosnjak, V; Mudd, SH; Pazanin, L; Pogribny, IP; Rados, M; Sarnavka, V; Schulze, A; Scukanec-Spoljar, M; Stabler, S; Uzelac, L; Vugrek, O; Wagner, C; Zeisel, S	1
Hirayama, M; Irie, M; Nakajima, H; Suwa, S; Wada, Y	1
Karlin, R	1

Reviews

1 review(s) available for methionine and Genetic Diseases

Article	Year
Ethical issues in human prion diseases. British medical bulletin, 2003, Volume: 66 Topics: Adolescent; Adult; Aged; Amyloid; Anonymous Testing; Appendix; Child; Diet; Ethics, Clinical; Female; Genetic Diseases, Inborn; Genetic Testing; Homozygote; Human Experimentation; Humans; Legislation, Medical; Male; Methionine; Middle Aged; Palatine Tonsil; Polymorphism, Genetic; Pregnancy; Preimplantation Diagnosis; Prion Diseases; Prion Proteins; Prions; Protein Precursors; PrPSc Proteins; Randomized Controlled Trials as Topic; Risk Assessment; United Kingdom	2003

Article

Year

Ethical issues in human prion diseases.

British medical bulletin, 2003, Volume: 66

Topics: Adolescent; Adult; Aged; Amyloid; Anonymous Testing; Appendix; Child; Diet; Ethics, Clinical; Female; Genetic Diseases, Inborn; Genetic Testing; Homozygote; Human Experimentation; Humans; Legislation, Medical; Male; Methionine; Middle Aged; Palatine Tonsil; Polymorphism, Genetic; Pregnancy; Preimplantation Diagnosis; Prion Diseases; Prion Proteins; Prions; Protein Precursors; PrPSc Proteins; Randomized Controlled Trials as Topic; Risk Assessment; United Kingdom

2003

Other Studies

3 other study(ies) available for methionine and Genetic Diseases

Article	Year
S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism. Proceedings of the National Academy of Sciences of the United States of America, 2004, Mar-23, Volume: 101, Issue:12 Topics: Adenosylhomocysteinase; Brain; Genetic Diseases, Inborn; Humans; Infant; Infant, Newborn; Liver; Magnetic Resonance Imaging; Male; Methionine; Radiography; Ultrasonography	2004
Newborn mass screening in Japan--1984. Jinrui idengaku zasshi. The Japanese journal of human genetics, 1984, Volume: 29, Issue:3 Topics: Congenital Hypothyroidism; Genetic Diseases, Inborn; Genetic Testing; Humans; Hypothyroidism; Infant, Newborn; Japan; Mass Screening; Metabolism, Inborn Errors; Methionine	1984
[Correlations among the amounts of B 12, methionine and folates in the blood of mothers of hypotrophic infants]. Annales de la nutrition et de l'alimentation, 1969, Volume: 23, Issue:2 Topics: Biological Assay; Birth Weight; Diet; Female; Folic Acid; Genetic Diseases, Inborn; Humans; Infant, Newborn; Lactobacillus; Leuconostoc; Male; Methionine; Nutritional Requirements; Postpartum Period; Pregnancy; Statistics as Topic; Vitamin B 12	1969