s-adenosylmethionine has been researched along with Fasting Hypoglycemia in 22 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (4.55) | 18.2507 |
| 2000's | 7 (31.82) | 29.6817 |
| 2010's | 12 (54.55) | 24.3611 |
| 2020's | 2 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| He, R; Huang, M; Kang, L; Li, X; Li, Y; Liu, Y; Ma, R; Men, J; Ren, J; Song, J; Yang, Y | 1 |
| Cheng, RQ; Hussain, K; Lu, W; Luo, FH; Ni, JW; Sun, WH; Xi, L; Xu, ZR; Zhang, MY; Zhu, XY | 1 |
| De Bernardis, NP; Divers, TJ; Pinn, TL; Southard, T; Valberg, S; Wakshlag, JJ | 1 |
| Cusmano-Ozog, K; McGuire, PJ; Tarasenko, TN | 1 |
| Phowthongkum, P; Shotelersuk, V; Suphapeetiporn, K | 1 |
| Derks, TGJ; Heiner-Fokkema, MR; van der Ende, RM; van Rijt, WJ; van Spronsen, F; Volker-Touw, CML | 1 |
| Bick, DP; Burrage, LC; Craigen, WJ; Elsea, SH; Gibson, JB; Graham, BH; Lose, EJ; Miller, MJ; Strenk, ME; Sun, Q; Sutton, VR; Wong, LJ; Zhang, VW | 1 |
| Fukuda, S; Hasegawa, Y; Kobayashi, H; Purevsuren, J; Takahashi, T; Yamada, K; Yamaguchi, S | 1 |
| Alam, S; Gupta, PK; Khanna, R; Rawat, D; Sarin, SK; Sharma, S; Sood, V | 1 |
| Alt, FW; Bain, JR; Biddinger, S; Farese, RV; Goetzman, E; Grueter, CA; Harris, C; Hirschey, MD; Ilkayeva, OR; Jing, E; Kahn, CR; Li, Y; Lombard, DB; Newgard, CB; Ruderman, NB; Saha, AK; Schwer, B; Shimazu, T; Stevens, RD; Verdin, E | 1 |
| Baruteau, J; Bloom, MC; Broué, P; Levade, T; Mesli, S; Redonnet-Vernhet, I | 1 |
| Gillingham, MB; Hirschfeld, M; Koeller, DM; Lambert, WE; Lowe, S; Matern, D; Shoemaker, J | 1 |
| Fukao, T; Fukuda, S; Hasegawa, Y; Kobayashi, H; Purevsuren, J; Takahashi, T; Takayanagi, M; Yamada, K; Yamaguchi, S | 1 |
| Champion, MP; Dalton, RN; Turner, C; Wraige, E | 1 |
| de Sain, MG; Dorland, L; Engbers, HM; Eskes, PF; Visser, G | 1 |
| Bodamer, OA; Hussein, K; Langhans, CD; Leonard, JV; Mayatepek, E; Morris, AA; Rating, D | 1 |
| Chakrapani, A; Gray, G; Hendriksz, C; Macdonald, A; Pierre, G; Preece, MA | 1 |
| Aleck, K; Ding, JH; Grebe, TA; He, G; Roe, CR; Roe, DS; Teramoto, R; Yang, BZ | 1 |
| Dorland, L; Duran, M; IJlst, L; Muntau, AC; Roscher, AA; Röschinger, W; Wanders, RJ | 1 |
| Aynsley-Green, A; Berger, R; Clayton, PT; Datta, V; Eaton, S; Edginton, M; Hussain, K; Krywawych, S; Malingre, HE; van den Berg, IE | 1 |
| Ballhausen, D; Blom, HJ; Dionisi-Vici, C; Dobbelaere, D; Douillard, C; Freisinger, P; Grünert, SC; Haas, D; Hoffmann, GF; Kahrizi, K; Kölker, S; la Marca, G; Lindner, M; Makhseed, N; Staufner, C; Straub, BK | 1 |
| Hovda, LR; Schmid, RD | 1 |
1 trial(s) available for s-adenosylmethionine and Fasting Hypoglycemia
| Article | Year |
|---|---|
Impaired fasting tolerance among Alaska native children with a common carnitine palmitoyltransferase 1A sequence variant.
Topics: Alaska; American Indian or Alaska Native; Body Mass Index; Carnitine; Carnitine O-Palmitoyltransferase; Child, Preschool; Fatty Acids, Nonesterified; Gas Chromatography-Mass Spectrometry; Homozygote; Humans; Hypoglycemia; Ketones; Lipid Metabolism, Inborn Errors; Polymorphism, Single Nucleotide; Tandem Mass Spectrometry | 2011 |
21 other study(ies) available for s-adenosylmethionine and Fasting Hypoglycemia
| Article | Year |
|---|---|
One potential hotspot ACADVL mutation in Chinese patients with very-long-chain acyl-coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Asian People; Carnitine; China; Congenital Bone Marrow Failure Syndromes; Female; Humans; Hypoglycemia; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver Diseases; Male; Mitochondrial Diseases; Muscular Diseases; Mutation | 2020 |
Altered Serum Amino Acid and Acylcarnitine Profiles in Hyperinsulinemic Hypoglycemia and Ketotic Hypoglycemia.
Topics: Amino Acids; Biomarkers; Carnitine; Case-Control Studies; Child, Preschool; Congenital Hyperinsulinism; Female; Follow-Up Studies; Humans; Hypoglycemia; Infant; Ketosis; Male; Prognosis; Retrospective Studies | 2020 |
Persistent hypoglycemia associated with lipid storage myopathy in a paint foal.
Topics: Animals; Carnitine; Diagnosis, Differential; Fatal Outcome; Female; Horse Diseases; Horses; Hypoglycemia; Lipid Metabolism, Inborn Errors; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscular Dystrophies | 2018 |
Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Animals; Cardiomyopathies; Carnitine; Congenital Bone Marrow Failure Syndromes; Disease Models, Animal; Fatty Acids; Female; Humans; Hypoglycemia; Lipid Metabolism, Inborn Errors; Lipid Peroxidation; Liver; Liver Failure; Metabolic Diseases; Mice; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Myocardium; Oxidation-Reduction | 2018 |
Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists.
Topics: Adult; Anti-Bacterial Agents; Carnitine; Carnitine O-Palmitoyltransferase; Escherichia coli Infections; Humans; Hypoglycemia; Lipid Metabolism, Inborn Errors; Liver; Male; Mutation, Missense; Non-alcoholic Fatty Liver Disease; Recurrence; Severity of Illness Index | 2019 |
Changes in pediatric plasma acylcarnitines upon fasting for refined interpretation of metabolic stress.
Topics: Blood Glucose; Carnitine; Child; Child, Preschool; Fasting; Female; Homeostasis; Humans; Hypoglycemia; Infant; Lipid Metabolism, Inborn Errors; Male; Retrospective Studies; Stress, Physiological | 2019 |
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Alleles; Carnitine; Computer Simulation; Congenital Bone Marrow Failure Syndromes; Exons; Female; Genetic Carrier Screening; Genotype; Humans; Hypoglycemia; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Muscular Diseases; Mutation, Missense; Neonatal Screening; Oligonucleotide Array Sequence Analysis; Sequence Analysis, DNA; Tandem Mass Spectrometry; United States | 2015 |
Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic Therapy.
Topics: Adolescent; Adult; Anti-Bacterial Agents; Brain Diseases; Carnitine; Child; Child, Preschool; Female; Humans; Hypoglycemia; Infant; Male; Retrospective Studies; Tandem Mass Spectrometry; Young Adult | 2016 |
Study of Carnitine/Acylcarnitine and Amino Acid Profile in Children and Adults With Acute Liver Failure.
Topics: Adolescent; Adult; Amino Acids; Biomarkers; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Hypoglycemia; Infant; Lipid Metabolism, Inborn Errors; Liver Failure, Acute; Liver Transplantation; Male; Patient Acuity; Prospective Studies | 2017 |
SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation.
Topics: Acetylation; Acyl-CoA Dehydrogenase, Long-Chain; Adenosine Triphosphate; Adipose Tissue, Brown; Animals; Body Temperature Regulation; Caloric Restriction; Carnitine; Cell Line; Cold Temperature; Fasting; Fatty Acids; Humans; Hypoglycemia; Liver; Male; Mass Spectrometry; Mice; Mitochondria; Oxidation-Reduction; Sirtuin 3; Triglycerides; Up-Regulation | 2010 |
Hypoketotic hypoglycemia with myolysis and hypoparathyroidism: an unusual association in medium chain acyl-CoA desydrogenase deficiency (MCADD).
Topics: Acute Kidney Injury; Acyl-CoA Dehydrogenase; Carnitine; Child, Preschool; Female; Glucose; Humans; Hypoglycemia; Hypoparathyroidism; Ketones; Lipid Metabolism, Inborn Errors; Mutation, Missense; Vitamin B Complex | 2009 |
Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1.
Topics: Biological Transport; Cardiomyopathies; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Cells, Cultured; Fatty Acids; Fibroblasts; Humans; Hyperammonemia; Hypoglycemia; Lipid Metabolism, Inborn Errors; Mitochondria; Muscular Diseases; Oxidation-Reduction; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry | 2013 |
Fat oxidation defect presenting with overwhelming ketonuria.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Brain Diseases, Metabolic; Carnitine; Female; Humans; Hypoglycemia; Infant; Ketone Bodies; Oxidation-Reduction | 2002 |
Rhabdomyolysis in early-onset very long-chain acyl-CoA dehydrogenase deficiency despite normal glucose after fasting.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Blood Glucose; Carnitine; Fasting; Glucose; Humans; Hypoglycemia; Infant; Metabolism, Inborn Errors; Rhabdomyolysis | 2005 |
Glucose and leucine kinetics in idiopathic ketotic hypoglycaemia.
Topics: Alanine; Amino Acids, Branched-Chain; Basal Metabolism; Calorimetry, Indirect; Carnitine; Case-Control Studies; Child; Child, Preschool; Fasting; Female; Glucose; Humans; Hypoglycemia; Infant; Insulin; Ketosis; Leucine; Male | 2006 |
Prospective treatment in carnitine-acylcarnitine translocase deficiency.
Topics: Carnitine; Carnitine Acyltransferases; Dicarboxylic Acids; Diet, Fat-Restricted; Dietary Supplements; Fatty Acids; Humans; Hyperammonemia; Hypoglycemia; Infant; Male; Membrane Transport Proteins; Metabolism, Inborn Errors; Oxidation-Reduction; Pedigree; Phenotype; Severity of Illness Index; Treatment Outcome | 2007 |
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Alleles; Carnitine; Child, Preschool; DNA, Complementary; Exons; Female; Fibroblasts; Humans; Hypoglycemia; Mitochondria; Mutation; Palmitoylcarnitine; Phenotype | 1999 |
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle.
Topics: Ammonia; Cardiac Output, Low; Carnitine; Carnitine Acyltransferases; Cells, Cultured; Coma; Consanguinity; Dicarboxylic Acids; Fatal Outcome; Female; Fibroblasts; Humans; Hypoglycemia; Infant, Newborn; Lactic Acid; Mass Spectrometry; Mitochondria; Pregnancy; Seizures; Uric Acid | 2000 |
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Amino Acid Sequence; Animals; Base Sequence; Carnitine; DNA Primers; Evolution, Molecular; Fatty Acids; Female; Gene Expression; Homozygote; Humans; Hyperinsulinism; Hypoglycemia; In Vitro Techniques; Infant; Insulin; Insulin Secretion; Models, Biological; Molecular Sequence Data; Oxidation-Reduction; Point Mutation; Recombinant Proteins; Sequence Homology, Amino Acid | 2001 |
Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options.
Topics: Adenosine; Adenosine Kinase; Adolescent; Adult; Biomarkers; Child; Child, Preschool; Diet; Female; Humans; Hypoglycemia; Infant; Liver; Liver Diseases; Male; Metabolic Diseases; Methionine; Retrospective Studies; S-Adenosylhomocysteine; S-Adenosylmethionine; Young Adult | 2016 |
Acute Hepatic Failure in a Dog after Xylitol Ingestion.
Topics: Acetylcysteine; Animals; Animals, Inbred Strains; Antidotes; Biomarkers; Chemical and Drug Induced Liver Injury; Combined Modality Therapy; Disseminated Intravascular Coagulation; Dogs; Hypoglycemia; Liver Failure, Acute; Male; S-Adenosylmethionine; Sweetening Agents; Treatment Outcome; Xylitol | 2016 |