methionine has been researched along with Anemia, Megaloblastic in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 18 (72.00) | 18.7374 |
| 1990's | 5 (20.00) | 18.2507 |
| 2000's | 1 (4.00) | 29.6817 |
| 2010's | 1 (4.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bard, G; Barlogis, V; Giraudier, S; Hamel, C; Moat, SJ; Odent, S; Ogier de Baulny, H; Schiff, M; Shortland, G; Touati, G | 1 |
| Fowler, B; Kozich, V; Pristoupilová, K; Suormala, T; Zavad'áková, P; Zavadakova, P; Zeman, J | 1 |
| HERBERT, V; SULLIVAN, LW | 1 |
| Cooper, BA; Grauer, K; Lue-Shing, H; Matiaszuk, N; Pottier, A; Rosenblatt, DS | 1 |
| Bishop, AJ; Cooper, BA; Haworth, JC; Rosenblatt, DS; Schroeder, ML; Schuh, S; Seargeant, LE | 1 |
| Chanarin, I; Deacon, R; Lumb, M; Perry, J | 3 |
| Bedros, AA; Carmel, R; Goodman, SI; Mace, JW | 1 |
| Burnett, AK; Ramsahoye, BH; Taylor, C | 1 |
| Arnold, G; Barness, LA; Harding, CO; Rosenblatt, DS; Wolff, JA | 1 |
| Braeuer, HC; Kohlschütter, A; Rosenblatt, DS; Scheying, H; Steen, C | 1 |
| Gravel, RA; Leclerc, D; Rosenblatt, DS; Wilson, A | 1 |
| Duvaltier, I; Labrune, P; Marquet, J; Niaudet, P; Odièvre, M; Trioche, P; Zittoun, J | 1 |
| Das, KC; Herbert, V | 1 |
| Nunn, JF | 1 |
| Cooper, BA | 1 |
| Arenson, E; Begley, JA; Chu, RC; Hall, CA; Lindenbaum, RH | 1 |
| Rosenblatt, DS; Watkins, D | 2 |
| Chanarin, I; Deacon, R; Lumb, M; Muir, M; Perry, J | 1 |
| Karasawa, M; Maekawa, T; Omine, M; Yamauchi, H | 1 |
| Cooper, BA; Erbe, RW; Rosenblatt, DS; Thomas, IT; Watkins, D | 1 |
| Corbeel, L; Eeckels, R; Jaeken, J; Van den Berghe, G; Van Tornout, J | 1 |
7 review(s) available for methionine and Anemia, Megaloblastic
| Article | Year |
|---|---|
Nitrous oxide, vitamin B12 deficiency and the methyl folate trap.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; Animals; Humans; Liver; Macaca fascicularis; Methionine; Methylmalonyl-CoA Mutase; Nervous System Diseases; Nitrous Oxide; Rats; S-Adenosylhomocysteine; S-Adenosylmethionine; Tetrahydrofolates; Vitamin B 12 Deficiency | 1982 |
Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Macrocytic; Anemia, Megaloblastic; Anorexia; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Genetic Complementation Test; Homocystine; Homocystinuria; Humans; Male; Methionine; Skin; Vitamin B 12 | 1997 |
Anesthesia and the leucocyte.
Topics: Anemia, Megaloblastic; Anesthetics; Animals; Bone Marrow; Cell Movement; Chemotaxis, Leukocyte; Halothane; Humans; Liver; Methionine; Neutropenia; Neutrophils; Nitrous Oxide; Phagocytosis; Rats; Spinal Cord; Thymidine; Vitamin B 12 | 1979 |
Megaloblastic anaemia and disorders affecting utilisation of vitamin B12 and folate in childhood.
Topics: Adolescent; Adult; Anemia, Hemolytic; Anemia, Macrocytic; Anemia, Megaloblastic; Anemia, Pernicious; Biological Transport; Bone Marrow; Bone Marrow Cells; Child; Child, Preschool; Female; Folic Acid; Folic Acid Deficiency; Homocystinuria; Humans; Infant; Intrinsic Factor; Malabsorption Syndromes; Male; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Orotic Acid; Phenylketonurias; Tetrahydrofolate Dehydrogenase; Transcobalamins; Vitamin B 12 | 1976 |
Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Anemia, Megaloblastic; Cells, Cultured; Female; Fibroblasts; Genetic Complementation Test; Homocystinuria; Humans; Infant; Infant, Newborn; Male; Methionine; Methyltransferases; Nervous System Diseases; Vitamin B 12 | 1989 |
Cobalamin-folate interrelations.
Topics: Anemia, Megaloblastic; Animals; Central Nervous System Diseases; Coenzymes; Folic Acid; Folic Acid Deficiency; Formates; Humans; Methionine; Models, Biological; Tetrahydrofolates; Thymidine; Vitamin B 12; Vitamin B 12 Deficiency | 1989 |
Cobalamin-folate interrelations: a critical review.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; Animals; Central Nervous System; Deoxyuridine; Disease Models, Animal; Drug Interactions; Enzyme Activation; Folic Acid; Folic Acid Deficiency; Histidine; Humans; Liver; Methionine; Methylmalonyl-CoA Mutase; Nitrous Oxide; Oxidation-Reduction; Pteroylpolyglutamic Acids; Purines; Serine; Tetrahydrofolates; Thymidylate Synthase; Vitamin B 12; Vitamin B 12 Deficiency | 1985 |
18 other study(ies) available for methionine and Anemia, Megaloblastic
| Article | Year |
|---|---|
Should transcobalamin deficiency be treated aggressively?
Topics: Anemia, Megaloblastic; Biological Transport; DNA Mutational Analysis; DNA Primers; Female; Homocysteine; Humans; Infant; Infant, Newborn; Methionine; Methylmalonic Acid; Mutation; Polymerase Chain Reaction; Protein Structure, Tertiary; Transcobalamins | 2010 |
CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families.
Topics: Adult; Anemia, Megaloblastic; Base Sequence; Cells, Cultured; Child; Chromatography, Ion Exchange; DNA; Female; Ferredoxin-NADP Reductase; Fibroblasts; Folic Acid; Homocysteine; Homocystinuria; Humans; Methionine; Molecular Sequence Data; Mutation; Prenatal Diagnosis; Reverse Transcriptase Polymerase Chain Reaction; Serine; Vitamin B 12 | 2002 |
Formiminoglutamicaciduria in humans with megaloblastic anemia: diminution by methionine or glycine.
Topics: Amino Acids; Anemia; Anemia, Macrocytic; Anemia, Megaloblastic; Glutamates; Glycine; Methionine; Serine | 1963 |
Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Macrocytic; Anemia, Megaloblastic; Cells, Cultured; Fibroblasts; Homocystinuria; Humans; Methionine; Nitrous Oxide; Vitamin B 12 | 1984 |
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Amino Acid Metabolism, Inborn Errors; Anemia, Macrocytic; Anemia, Megaloblastic; Cobamides; Fibroblasts; Homocystinuria; Humans; Hydroxocobalamin; Infant, Newborn; Male; Methionine; Propionates; Tetrahydrofolates; Vitamin B 12 | 1984 |
How vitamin B12 acts.
Topics: Anemia, Macrocytic; Anemia, Megaloblastic; Animals; Folic Acid; Humans; Methionine; Pteroylpolyglutamic Acids; S-Adenosylmethionine; Thymidine; Vitamin B 12 Deficiency | 1981 |
Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test.
Topics: Anemia, Megaloblastic; Deoxyuridine; DNA; Female; Homocysteine; Homocystinuria; Humans; Hydroxocobalamin; Infant; Infant, Newborn; Malonates; Methionine; Methylmalonic Acid; Myoclonus; Thymidine | 1980 |
Nucleic acid composition of bone marrow mononuclear cells in cobalamin deficiency.
Topics: 5-Methylcytosine; Aged; Aged, 80 and over; Anemia, Megaloblastic; Artifacts; Bone Marrow; Chromatography, High Pressure Liquid; Cytosine; Deamination; DNA; DNA Glycosylases; Female; Humans; Male; Methionine; Methylation; Middle Aged; N-Glycosyl Hydrolases; Reproducibility of Results; Uracil; Uracil-DNA Glycosidase; Vitamin B 12 Deficiency | 1996 |
Cobalamin E (cblE) disease: a severe neurological disorder with megaloblastic anaemia, homocystinuria and low serum methionine.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Anemia, Megaloblastic; Brain Diseases; Homocystinuria; Humans; Male; Methionine; Vitamin B 12 | 1997 |
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; DNA Mutational Analysis; DNA, Complementary; Enzyme Activation; Ferredoxin-NADP Reductase; Folic Acid; Genes, Recessive; Genetic Complementation Test; Heteroduplex Analysis; Homocysteine; Humans; Hyperhomocysteinemia; Methionine; Mutation; Polymorphism, Single-Stranded Conformational; Reverse Transcriptase Polymerase Chain Reaction; RNA Splicing; Sequence Analysis, DNA; Vitamin B 12 | 1999 |
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; Female; Hemolytic-Uremic Syndrome; Humans; Hypertension, Pulmonary; Infant; Metabolism, Inborn Errors; Methionine; Vitamin B 12 | 1999 |
Vitamin B12--folate interrelations.
Topics: Anemia, Megaloblastic; DNA; Folic Acid; Folic Acid Deficiency; Formiminoglutamic Acid; Glycine; Homocysteine; Humans; Methionine; Methylmalonyl-CoA Mutase; Nervous System Diseases; Vitamin B 12; Vitamin B 12 Deficiency | 1976 |
The nature of the defect in cobalamin G mutation.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; Cell Division; Cells, Cultured; Female; Fibroblasts; Humans; Infant; Male; Methionine; Mutation; S-Adenosylmethionine; Transcobalamins; Vitamin B 12 | 1989 |
Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Macrocytic; Anemia, Megaloblastic; Cells, Cultured; Fibroblasts; Genetic Complementation Test; Homocystinuria; Humans; Methionine; Mutation; Vitamin B 12; Vitamin B 12 Deficiency | 1988 |
Methionine partially corrects the impaired deoxyribonucleic acid synthesis of B12-deficient megaloblastic bone marrow cells at low concentration.
Topics: Anemia, Macrocytic; Anemia, Megaloblastic; Anemia, Pernicious; Bone Marrow; Deoxyuridine; DNA; Homocysteine; Humans; Methionine; Vitamin B 12 Deficiency | 1986 |
Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
Topics: Anemia, Macrocytic; Anemia, Megaloblastic; Cells, Cultured; Fibroblasts; Homocysteine; Homocystinuria; Humans; Infant; Male; Methionine; Vitamin B 12; Vitamin B 12 Deficiency | 1987 |
Congenital folate malabsorption.
Topics: Anemia, Macrocytic; Anemia, Megaloblastic; Biological Transport; Blood-Brain Barrier; Brain Diseases; Calcinosis; Female; Folic Acid; Folic Acid Deficiency; Humans; Infant; Infections; Intellectual Disability; Intestinal Absorption; Methionine; Seizures | 1985 |
Role of folate dependent transformylases in synthesis of purine in bone marrow of man and in bone marrow and liver of rats.
Topics: Acyltransferases; Adenosine; Anemia, Megaloblastic; Animals; Bone Marrow; Deoxyadenosines; Humans; Hydroxymethyl and Formyl Transferases; Liver; Male; Methionine; Nitrous Oxide; Phosphoribosylaminoimidazolecarboxamide Formyltransferase; Phosphoribosylglycinamide Formyltransferase; Purines; Rats; Rats, Inbred Strains; Thionucleosides; Vitamin B 12; Vitamin B 12 Deficiency | 1985 |