Compounds > methionine
Page last updated: 2024-08-17

methionine and Abnormalities, Multiple

methionine has been researched along with Abnormalities, Multiple in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19903 (75.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abdulsabur, N; Antshel, KM; Colgan, D; Fremont, W; Funke, B; Higgins, AM; Kates, WR; Kucherlapati, R; Shprintzen, RJ1
Hashimoto, T; Schram, AW; Schutgens, RB; Strijland, A; Tager, JM; van den Bosch, H; Wanders, RJ1
Bartsocas, CS; Crawford, JD1
Narayanan, HS; Rao, R; Reddy, GN; Sridhara, BS1

Other Studies

4 other study(ies) available for methionine and Abnormalities, Multiple

ArticleYear
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2006, Apr-05, Volume: 141B, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Alleles; Brain; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; DNA Mutational Analysis; Face; Female; Gene Frequency; Genotype; Heart Defects, Congenital; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Sex Factors; Syndrome; Task Performance and Analysis; Valine; Velopharyngeal Insufficiency

2006
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
    Proceedings of the National Academy of Sciences of the United States of America, 1986, Volume: 83, Issue:16

    Topics: Abnormalities, Multiple; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acyl-CoA Oxidase; Catalase; Cell Line; Diffuse Cerebral Sclerosis of Schilder; Fibroblasts; Humans; Infant; Leucine; Methionine; Microbodies; Oxidation-Reduction; Oxidoreductases; Reference Values; Refsum Disease; Syndrome

1986
Clinical phenotypes in kidney transport disorders.
    Birth defects original article series, 1974, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Acidosis, Renal Tubular; Cerebrospinal Fluid Proteins; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria; Diabetes Insipidus; Galactose; Glucose; Glycosuria, Renal; Growth Disorders; Hartnup Disease; Humans; Hypophosphatemia, Familial; Kidney Tubules; Malabsorption Syndromes; Methionine; Phenotype; Pseudohypoparathyroidism; Pulmonary Heart Disease; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Seizures; Syndrome

1974
Homocystinuria in three Indian children.
    The Indian journal of medical research, 1971, Volume: 59, Issue:4

    Topics: Abnormalities, Multiple; Child; Child, Preschool; Diagnosis, Differential; Female; Homocystinuria; Humans; Intellectual Disability; Male; Methionine

1971