Compounds > succinyl-coenzyme a
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succinyl-coenzyme a and Amino Acid Metabolism Disorders, Inborn

succinyl-coenzyme a has been researched along with Amino Acid Metabolism Disorders, Inborn in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's4 (66.67)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Anvar, Z; Faghihi, MA; Farazi Fard, MA; Habibzadeh, P; Hafizi, A; Jamali, L; Nasr Esfahani, MH; Nikuei, P; Salarian, L; Tabatabaei, Z1
Bicakci, Z1
Gotoh, K; Hotta, Y; Ito, T; Kataoka, T; Kawade, Y; Kimura, K; Maeda, Y; Nakajima, Y; Sugiyama, N; Tajima, G1
Craigen, WJ; Donti, TR; Graham, BH; Masand, R; Scott, DA1
Abukawa, D; Haginoya, K; Harashima, H; Kure, S; Miyabayashi, S; Murayama, K; Ohtake, A; Ohura, T; Sakamoto, O; Takeyama, J1
Carlucci, F; Rosi, F; Tabucchi, A; Tommassini, V1

Other Studies

6 other study(ies) available for succinyl-coenzyme a and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene.
    BMC medical genetics, 2020, 02-03, Volume: 21, Issue:1

    Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Child; Female; High-Throughput Nucleotide Sequencing; Homozygote; Humans; Infant; Infant, Newborn; Iran; Male; Methylmalonyl-CoA Mutase; Mutation, Missense; Phenotype; Pregnancy; Preimplantation Diagnosis

2020
Growth retardation, general hypotonia, and loss of acquired neuromotor skills in the infants of mothers with cobalamin deficiency and the possible role of succinyl-CoA and glycine in the pathogenesis.
    Medicine, 2015, Volume: 94, Issue:9

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Anemia; Female; Gluconeogenesis; Glycine; Growth Disorders; Hematopoiesis; Humans; Infant; Male; Mothers; Motor Skills; Muscle Hypotonia; Nervous System Diseases; Pregnancy; Pregnancy Complications; Vitamin B 12; Vitamin B 12 Deficiency

2015
Assay for methylmalonyl coenzyme A mutase activity based on determination of succinyl coenzyme A by ultrahigh-performance liquid chromatography tandem mass spectrometry.
    Analytical and bioanalytical chemistry, 2015, Volume: 407, Issue:18

    Topics: Acyl Coenzyme A; Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; Enzyme Assays; Female; Humans; Male; Methylmalonyl-CoA Mutase; Sensitivity and Specificity; Tandem Mass Spectrometry; Young Adult

2015
Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variant.
    Molecular genetics and metabolism, 2016, Volume: 119, Issue:1-2

    Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Child; DNA, Mitochondrial; Exome Sequencing; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Mitochondria; Mutation, Missense; Succinate-CoA Ligases

2016
Neonatal lactic acidosis with methylmalonic aciduria due to novel mutations in the SUCLG1 gene.
    Pediatrics international : official journal of the Japan Pediatric Society, 2011, Volume: 53, Issue:6

    Topics: Acidosis, Lactic; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Blotting, Western; DNA; DNA Mutational Analysis; Fatal Outcome; Female; Humans; Infant, Newborn; Mutation

2011
CE assay of methylmalonyl-coenzyme-a mutase activity.
    Electrophoresis, 2007, Volume: 28, Issue:12

    Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Buffers; Electrophoresis, Capillary; Humans; Liver; Lymphocytes; Methylmalonic Acid; Methylmalonyl-CoA Mutase; Rats; Rats, Wistar; Reproducibility of Results; Sensitivity and Specificity; Spectrophotometry, Ultraviolet

2007