isoleucine and Symptom Cluster

isoleucine has been researched along with Symptom Cluster in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (25.00)	18.7374
1990's	3 (18.75)	18.2507
2000's	7 (43.75)	29.6817
2010's	2 (12.50)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abudu, H; Ahemaiti, A; Aximujiang, K; Wu, G; Yunusi, K; Zhang, J	1
Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV	1
Baal, C; Hemmer, W; Jarisch, R; Litschauer-Poursadrollah, M; Mayer, DE	1
Drenth, JP; Mariman, EC; Simon, A; van der Meer, JW	1
SIEGAL, S	1
Naito, K; Shiraishi, K	1
Barshop, BA; Haas, RH; McGowan, KA; Naviaux, RK; Nyhan, WL; Townsend, JJ; Yu, A	1
Beani, JC; Boujet, C; Lantuejoul, S; Leccia, MT; Nguyen, MA; Reymond, JL; Templier, I	1
Bennett, MJ; Bertini, E; Burlina, AB; Dionisi-Vici, C; Gibson, KM; Hale, DE; Sabetta, G; Schmidt-Sommerfeld, E; Servidei, S; Zacchello, F	1
Berry, GT; Giacoia, GP	1
Abeling, NG; Bakker, HD; Bosch, AM; Schutgens, RB; Sillevis Smitt, JH; Van Gennip, AH; Wijburg, FA	1
Mickelson, JR; Purdy, AK; Santschi, EM; Vrotsos, PD	1
de Smet, MD; Jager, MJ; Ongkosuwito, JV; Rozemuller, EH; Suttorp-Schulten, MS; Tilanus, MG; Van der Lelij, A; van Schooneveld, MJ	1
Porath, U; Schreier, K	1
Feigin, RD; Hillman, RE; Keating, JP; Tenenbaum, SM	1
Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M	1

Reviews

1 review(s) available for isoleucine and Symptom Cluster

Article	Year
[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

Article

Year

[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

15 other study(ies) available for isoleucine and Symptom Cluster

Article	Year
[Metabonomic analysis of the urine from rat model with abnormal sapra syndrome]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2017, Oct-28, Volume: 42, Issue:10 Topics: Amino Acids; Animals; Citric Acid; Creatine; Disease Models, Animal; Energy Metabolism; Glutamine; Glycoproteins; Isoleucine; Leucine; Metabolomics; Phenylalanine; Rats; Rats, Wistar; Syndrome	2017
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome. The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:10 Topics: Amino Acid Sequence; Blotting, Western; Deafness; DNA Mutational Analysis; Electrophoretic Mobility Shift Assay; Fluorescent Antibody Technique; GATA3 Transcription Factor; Humans; Hypoparathyroidism; Immunohistochemistry; Infant; Isoleucine; Kidney; Kidney Diseases; Male; Molecular Sequence Data; Mutation, Missense; Syndrome; Threonine	2009
Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2010, Volume: 8, Issue:2 Topics: Amino Acid Substitution; Child; Chromosome Aberrations; Chromosomes, Human, Pair 17; Dental Enamel Hypoplasia; Dental Pulp Cavity; Dermatitis, Atopic; DNA Mutational Analysis; Ectodermal Dysplasia; Female; Genes, Dominant; Hair; Homeodomain Proteins; Humans; Isoleucine; Microscopy, Electron; Phenotype; Serine; Syndrome; Tooth Abnormalities; Transcription Factors	2010
A founder effect in the hyperimmunoglobulinemia D and periodic fever syndrome. The American journal of medicine, 2003, Feb-01, Volume: 114, Issue:2 Topics: Alleles; Europe; Familial Mediterranean Fever; Female; Founder Effect; Humans; Hypergammaglobulinemia; Immunoglobulin D; Isoleucine; Linkage Disequilibrium; Male; Pedigree; Syndrome; Valine	2003
THE THALASSEMIA SYNDROMES. BIOCHEMICAL, GENETIC AND CLINICAL CONSIDERATIONS. The American journal of medicine, 1964, Volume: 36 Topics: Biochemical Phenomena; Biochemistry; DNA; Genetics, Medical; Hemoglobins; Hemoglobins, Abnormal; Isoleucine; Leucine; Proteins; Reticulocytes; RNA; Syndrome; Thalassemia	1964
Fertile eunuch syndrome with the mutations (Trp8Arg and Ile15Thr) in the beta subunit of luteinizing hormone. Endocrine journal, 2003, Volume: 50, Issue:6 Topics: Adolescent; Arginine; Base Sequence; Biopsy; DNA; Eunuchism; Fertility; Gene Amplification; Genitalia, Male; Humans; Isoleucine; Luteinizing Hormone, beta Subunit; Male; Mutation; Osmolar Concentration; Polymerase Chain Reaction; Syndrome; Testis; Testosterone; Threonine; Tryptophan	2003
The role of methionine in ethylmalonic encephalopathy with petechiae. Archives of neurology, 2004, Volume: 61, Issue:4 Topics: Amino Acids; Brain; Brain Diseases, Metabolic, Inborn; Caudate Nucleus; Fatal Outcome; Female; Follow-Up Studies; Humans; Infant; Isoleucine; Male; Malonates; Methionine; Pedigree; Purpura; Substantia Nigra; Syndrome	2004
[Acrodermatitis enteropathica-like syndrome secondary to branched-chain amino acid deficiency during treatment of maple syrup urine disease]. Annales de dermatologie et de venereologie, 2006, Volume: 133, Issue:4 Topics: Acrodermatitis; Female; Humans; Infant; Isoleucine; Maple Syrup Urine Disease; Syndrome; Valine	2006
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts. The Journal of pediatrics, 1994, Volume: 124, Issue:1 Topics: Acyl-CoA Dehydrogenase; Brain; Chronic Disease; Cyanosis; Diarrhea; Fatty Acid Desaturases; Fatty Acids; Fibroblasts; Humans; Infant; Intellectual Disability; Isoleucine; Male; Malonates; Oxidation-Reduction; Paralysis; Purpura; Syndrome	1994
Acrodermatitis enteropathica-like syndrome secondary to isoleucine deficiency during treatment of maple syrup urine disease. American journal of diseases of children (1960), 1993, Volume: 147, Issue:9 Topics: Acrodermatitis; Humans; Iatrogenic Disease; Infant Food; Infant, Newborn; Isoleucine; Male; Maple Syrup Urine Disease; Syndrome	1993
Iatrogenic isolated isoleucine deficiency as the cause of an acrodermatitis enteropathica-like syndrome. The British journal of dermatology, 1998, Volume: 139, Issue:3 Topics: Acrodermatitis; Diarrhea, Infantile; Female; Humans; Iatrogenic Disease; Infant, Newborn; Isoleucine; Syndrome	1998
Incidence of the endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses. American journal of veterinary research, 2001, Volume: 62, Issue:1 Topics: Amino Acid Substitution; Animals; Female; Fetal Death; Genes, Lethal; Genetic Carrier Screening; Hair Color; Homozygote; Horse Diseases; Horses; Isoleucine; Lysine; Mutation; Pregnancy; Receptor, Endothelin B; Receptors, Endothelin; Syndrome	2001
Amino acid residue 67 (isoleucine) of HLA-DRB is associated with POHS. Investigative ophthalmology & visual science, 2002, Volume: 43, Issue:6 Topics: Alleles; DNA; Eye Infections, Fungal; Female; Histocompatibility Testing; Histoplasmosis; HLA-B7 Antigen; HLA-DR2 Antigen; Humans; Isoleucine; Male; Netherlands; Syndrome	2002
Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report. Pediatrics, 1972, Volume: 50, Issue:6 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Diet Therapy; Dietary Proteins; Female; Fibroblasts; Glycine; Humans; Infant; Isoleucine; Syndrome	1972
Amino acid abnormality in Sjögren-Larsson syndrome. Archives of neurology, 1973, Volume: 28, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine	1973