isoleucine and Acetonemia

isoleucine has been researched along with Acetonemia in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19908 (80.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brandon, P; Constance, LSL; Rajan, D1
Acquaviva-Bourdain, C; Benoist, JF; Bourillon, A; de Lonlay, P; Dobbelaere, D; Elmaleh-Bergès, M; Fouilhoux, A; Guffon, N; Labarthe, F; Mention, K; Ogier de Baulny, H; Paquay, S; Pichard, S; Rouvet, I; Schiff, M; Touati, G; Valayannopoulos, V; Vianey-Saban, C1
DANCIS, J; HUTZLER, J; LEVITZ, M1
SILBERMANSCHWARTZMAN, J1
Balfe, JW; Mamer, OA; Robinson, BH; Sherwood, WG; Taylor, J1
Porath, U; Schreier, K1
Grüttner, R; Held, KR; Plettner, C; Singh, S; Sternowsky, HJ2
Bartlett, K; Cannon, RA; Conde, C; Gomez Vazquez, J; Lipson, M; Middleton, B; Nyhan, WL; Romanos, A; Sweetman, L1
Chaussain, JL; Georges, P; Job, JC; Olive, G1

Reviews

1 review(s) available for isoleucine and Acetonemia

ArticleYear
[Congenital metabolic acidosis in the postnatal period].
    Deutsche medizinische Wochenschrift (1946), 1978, Jun-02, Volume: 103, Issue:22

    Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Glutarates; Glycogen Storage Disease Type I; Humans; Hyperglycemia; Infant, Newborn; Isoleucine; Ketosis; Lactates; Leucine; Leukoencephalitis, Acute Hemorrhagic; Methylmalonic Acid; Propionates; Syndrome; Thiamine; Valerates; Valine

1978

Other Studies

9 other study(ies) available for isoleucine and Acetonemia

ArticleYear
Beta-ketothiolase deficiency in a Malaysian infant.
    The Medical journal of Malaysia, 2019, Volume: 74, Issue:2

    Topics: Acetyl-CoA C-Acetyltransferase; Acetyl-CoA C-Acyltransferase; Adolescent; Amino Acid Metabolism, Inborn Errors; Humans; Isoleucine; Ketosis; Male; Sepsis

2019
Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis.
    Journal of inherited metabolic disease, 2017, Volume: 40, Issue:3

    Topics: Acetyl-CoA C-Acetyltransferase; Acetyl-CoA C-Acyltransferase; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Basal Ganglia; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Isoleucine; Ketone Bodies; Ketosis; Male; Mitochondria; Neonatal Screening; Retrospective Studies; Young Adult

2017
THE DIAGNOSIS OF MAPLE SYRUP URINE DISEASE (BRANCHED- CHAIN KETOACIDURIA) BY THE IN VITRO STUDY OF THE PERIPHERAL LEUKOCYTE.
    Pediatrics, 1963, Volume: 32

    Topics: Chromatography; Humans; In Vitro Techniques; Isoleucine; Keto Acids; Ketosis; Leucine; Leukocytes; Maple Syrup Urine Disease; Metabolism; Research; Valine

1963
[CLINICAL, BIOCHEMICAL, AND NEUROPATHOLOGIC ASPECTS OF MAPLE SYRUP URINE DISEASE. A KETOACIDURIA OF THE OPEN CHAIN AMINOACIDS LEUCINE, ISOLEUCINE AND VALINE].
    Anales. Universidad Nacional Mayor de San Marcos. Facultad de Medicina, 1963, Volume: 46

    Topics: Amino Acids; Genetics, Medical; Humans; Infant; Isoleucine; Keto Acids; Ketosis; Leucine; Maple Syrup Urine Disease; Nervous System Diseases; Neurosciences; Pathology; Valine

1963
Acetoacetyl CoA thiolase deficiency: a cause of severe ketoacidosis in infancy simulating salicylism.
    The Journal of pediatrics, 1979, Volume: 95, Issue:2

    Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acidosis; Adolescent; Carbon Dioxide; Child, Preschool; Chromatography, Gas; Deficiency Diseases; Diagnosis, Differential; Fatty Acids; Female; Humans; Isoleucine; Ketone Bodies; Ketosis; Mass Spectrometry; Oxidation-Reduction; Salicylates

1979
[Ketotic hypoglycemia in intermittent branch-chain ketoaciduria. Enzymatic and gas chromatographic studies].
    Monatsschrift fur Kinderheilkunde, 1976, Volume: 124, Issue:5

    Topics: Child; Chromatography, Gas; Female; Fibroblasts; Humans; Hypoglycemia; Isoleucine; Keto Acids; Ketosis; Leucine; Leukocytes; Valine

1976
[Intermittent branched--chain ketoacidurie in ketotic hypoglycemia: investigations to localize the biochemical defect (author's transl)].
    Monatsschrift fur Kinderheilkunde, 1976, Volume: 124, Issue:2

    Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child; Female; Fibroblasts; Humans; Hypoglycemia; Intellectual Disability; Isoleucine; Keto Acids; Ketosis; Leucine; Leukocytes; Valine

1976
3-Ketothiolase deficiency.
    European journal of pediatrics, 1986, Volume: 144, Issue:6

    Topics: 3-Hydroxybutyric Acid; Acetyl Coenzyme A; Acetyl-CoA C-Acyltransferase; Acyl Coenzyme A; Acyltransferases; Child; Female; Fibroblasts; Glycine; Humans; Hydroxybutyrates; Infant; Isoleucine; Ketosis; Male; Valerates

1986
Glycemic response to 24-hour fast in normal children and children with ketotic hypoglycemia: II. Hormonal and metabolic changes.
    The Journal of pediatrics, 1974, Volume: 85, Issue:6

    Topics: Acidosis; Alanine; Amino Acids; Autoanalysis; Blood Glucose; Child; Child, Preschool; Fasting; Fatty Acids, Nonesterified; Female; Glucagon; Growth Hormone; Hormones; Humans; Hydrocortisone; Hypoglycemia; Insulin; Isoleucine; Ketones; Ketosis; Leucine; Male; Valine

1974