homocysteine and BH4 Deficiency

homocysteine has been researched along with BH4 Deficiency in 20 studies

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19903 (15.00)18.7374
1990's0 (0.00)18.2507
2000's7 (35.00)29.6817
2010's7 (35.00)24.3611
2020's3 (15.00)2.80

Authors

AuthorsStudies
Kasyanov, ED; Kostina, OV; Mazo, GE; Piatoikina, AS; Rukavishnikov, GV; Semennov, IV; Verbitskaya, EV; Zhilyaeva, TV1
Evans, K; Glavin, F; Irwin, DE; Lapidus, D; Lew, CR; Sellos-Moura, M1
Akış, M; Arslan, N; Işık, İ; İşlekel, H; Kant, M; Kısa, PT; Köse, E1
Aldámiz-Echevarría, L; Andrade, F; Couce, ML; Llarena, M; López-Suárez, O1
Benáková, H; Haňková, Z; Jarkovský, J; Konečná, P; Mikušková, A; Procházková, D; Vinohradská, H1
Arslan, N; Çakar, S; Gündüz, M; Kuyum, P; Makay, B1
Banderali, G; Cefalo, G; Giovannini, M; Lassandro, C; Moretti, F; Radaelli, G; Salvatici, E; Verduci, E1
Aldámiz-Echevarría, L; Couce, ML; Fernández-Marmiesse, A; Hermida, A; Leis, R; Llarena, M; Roca, I; Sánchez-Pintos, P; Vitoria, I1
Fokkema, MR; Hoeksma, M; Monsen, AL; Reijngoud, DJ; van Rijn, M; van Spronsen, FJ; Vugteveen, I1
Bodamer, OA; Huemer, M; Mayr, D; Möslinger, D; Mühl, A; Schmid, I; Simma, B; Ulmer, H1
Green, A; Hall, K; Leeming, R; Lucock, M; MacDonald, A; Rylance, G; Yates, Z1
Karikas, GA; Papakonstantinou, E; Schulpis, KH1
Artuch, R; Brandi, N; Campistol, J; Colomé, C; Lambruschini, N; Sierra, C; Vilaseca, MA1
COFFEY, VP1
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D1
Chrousos, GP; Papassotiriou, I; Schulpis, KH; Tsakiris, S; Vounatsou, M1
Hvas, AM; Nexo, E; Nielsen, JB1
Bodamer, OA; Födinger, M; Herle, M; Huemer, M; Möslinger, D; Mühl, A; Stöckler-Ipsiroglu, S; Ulmer, H; Weigmann, C1
Baumann, N; Fontaine, B; Lubetzki, C; Lyon-Caen, O; Saudubray, JM; Sedel, F; Tourbah, A1
Gjessing, LR; Seip, M; Vellan, EJ1

Reviews

2 review(s) available for homocysteine and BH4 Deficiency

ArticleYear
Diet in children with phenylketonuria and risk of cardiovascular disease: A narrative overview.
    Nutrition, metabolism, and cardiovascular diseases : NMCD, 2016, Volume: 26, Issue:3

    Topics: Adiponectin; Arginine; Blood Pressure; Cardiovascular Diseases; Child; Cholesterol, HDL; Cholesterol, LDL; Diet; Homocysteine; Humans; Oxidative Stress; Pediatric Obesity; Phenylalanine; Phenylketonurias; Risk Factors

2016
Leukoencephalopathies associated with inborn errors of metabolism in adults.
    Journal of inherited metabolic disease, 2008, Volume: 31, Issue:3

    Topics: Adrenoleukodystrophy; Brain Diseases, Metabolic, Inborn; Electron Transport; Hereditary Central Nervous System Demyelinating Diseases; Homocysteine; Humans; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Magnetic Resonance Imaging; Phenylketonurias; Xanthomatosis, Cerebrotendinous

2008

Other Studies

18 other study(ies) available for homocysteine and BH4 Deficiency

ArticleYear
Tetrahydrobiopterin deficiency in schizophrenia: Biochemical and clinical aspects.
    Journal of psychiatric research, 2022, Volume: 153

    Topics: C-Reactive Protein; Case-Control Studies; Folic Acid; Homocysteine; Humans; Phenylketonurias; Schizophrenia; Vitamin B 12

2022
Prevalence, characteristics, and costs of diagnosed homocystinuria, elevated homocysteine, and phenylketonuria in the United States: a retrospective claims-based comparison.
    BMC health services research, 2020, Mar-06, Volume: 20, Issue:1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; Child, Preschool; Female; Health Care Costs; Homocysteine; Homocystinuria; Humans; Infant; Infant, Newborn; Insurance Claim Review; Male; Middle Aged; Phenylketonurias; Prevalence; Retrospective Studies; United States; Young Adult

2020
Functional vitamin B12 deficiency in phenylketonuria patients and healthy controls: An evaluation with combined indicator of vitamin B12 status as a biochemical index.
    Annals of clinical biochemistry, 2020, Volume: 57, Issue:4

    Topics: Adolescent; Biomarkers; Case-Control Studies; Child; Child, Preschool; Female; Folic Acid; Homocysteine; Humans; Male; Methylmalonic Acid; Phenylketonurias; Vitamin B 12; Vitamin B 12 Deficiency

2020
Influence of phenylketonuria's diet on dimethylated arginines and methylation cycle.
    Medicine, 2017, Volume: 96, Issue:27

    Topics: Arginine; Biomarkers; Child; Chromatography, High Pressure Liquid; Creatinine; Cross-Sectional Studies; Female; Folic Acid; Homocysteine; Humans; Male; Mass Spectrometry; Methylation; Patient Compliance; Phenylketonurias; Severity of Illness Index; Vitamin B 12

2017
Long-term treatment for hyperphenylalaninemia and phenylketonuria: a risk for nutritional vitamin B12 deficiency?
    Journal of pediatric endocrinology & metabolism : JPEM, 2015, Nov-01, Volume: 28, Issue:11-12

    Topics: Adolescent; Adult; Child; Child, Preschool; Female; Folic Acid; Homocysteine; Humans; Incidence; Male; Middle Aged; Phenylketonurias; Prospective Studies; Risk; Risk Assessment; Transcobalamins; Vitamin B 12 Deficiency; Young Adult

2015
Comparison of atherogenic risk factors among poorly controlled and well-controlled adolescent phenylketonuria patients.
    Cardiology in the young, 2016, Volume: 26, Issue:5

    Topics: Adolescent; Atherosclerosis; Biomarkers; Case-Control Studies; Child; Cholesterol, HDL; Female; Homocysteine; Humans; Male; Mean Platelet Volume; Phenylalanine; Phenylketonurias; Risk Factors; Turkey

2016
Lipid profile status and other related factors in patients with Hyperphenylalaninaemia.
    Orphanet journal of rare diseases, 2016, 09-09, Volume: 11, Issue:1

    Topics: Apolipoproteins A; Apolipoproteins B; Blood Pressure; C-Reactive Protein; Cholesterol; Cholesterol, HDL; Cholesterol, LDL; Coronary Disease; Cross-Sectional Studies; Female; Homocysteine; Humans; Lipids; Male; Methionine; Phenylketonurias; Risk Factors; Triglycerides; Vitamin B 12

2016
Serum vitamin B12 concentrations within reference values do not exclude functional vitamin B12 deficiency in PKU patients of various ages.
    Molecular genetics and metabolism, 2011, Volume: 102, Issue:1

    Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Female; Homocysteine; Humans; Infant; Male; Methylmalonic Acid; Phenylketonurias; Reference Values; Retrospective Studies; Vitamin B 12; Vitamin B 12 Deficiency; Young Adult

2011
Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU).
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:5

    Topics: Adolescent; Arginine; Atherosclerosis; Blood Glucose; Cardiovascular Diseases; Child; Cross-Sectional Studies; Female; Homocysteine; Humans; Lipid Metabolism; Male; Nitric Oxide; Nitric Oxide Synthase; Oxidative Stress; Phenylalanine; Phenylketonurias

2012
The impact of phenylketonuria on folate metabolism.
    Molecular genetics and metabolism, 2002, Volume: 76, Issue:4

    Topics: Biopterins; Chromatography, High Pressure Liquid; Coenzymes; Folic Acid; Homocysteine; Humans; Immunoassay; Phenylalanine; Phenylketonurias

2002
Homocysteine and other vascular risk factors in patients with phenylketonuria on a diet.
    Acta paediatrica (Oslo, Norway : 1992), 2002, Volume: 91, Issue:8

    Topics: Child; Child, Preschool; Coronary Artery Disease; Diet, Protein-Restricted; Endothelin-1; Folic Acid; Homocysteine; Humans; Lipids; Nutrition Assessment; Phenylalanine; Phenylketonurias; Risk Factors; Vitamin B 12; Vitamin B 6

2002
Plasma thiols and their determinants in phenylketonuria.
    European journal of clinical nutrition, 2003, Volume: 57, Issue:8

    Topics: Adolescent; Cross-Sectional Studies; Cysteine; Female; Folic Acid; Glutathione; Homocysteine; Humans; Male; Methionine; Phenylalanine; Phenylketonurias; Sulfhydryl Compounds; Vitamin B 12

2003
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    Journal of the Irish Medical Association, 1964, Volume: 54

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency

1964
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    The New England journal of medicine, 1964, Jun-25, Volume: 270

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine

1964
Increased plasma adiponectin concentrations in poorly controlled patients with phenylketonuria normalize with a strict diet: evidence for catecholamine-mediated adiponectin regulation and a complex effect of phenylketonuria diet on atherogenesis risk fact
    Metabolism: clinical and experimental, 2005, Volume: 54, Issue:10

    Topics: Adiponectin; Arteriosclerosis; Catecholamines; Child; Child, Preschool; Cholesterol, LDL; Female; Homocysteine; Humans; Intercellular Signaling Peptides and Proteins; Male; Phenylketonurias; Risk Factors; Tumor Necrosis Factor-alpha

2005
Vitamin B12 and vitamin B6 supplementation is needed among adults with phenylketonuria (PKU).
    Journal of inherited metabolic disease, 2006, Volume: 29, Issue:1

    Topics: Adolescent; Adult; Diet, Protein-Restricted; Female; Folic Acid; Homocysteine; Humans; Male; Phenylketonurias; Transcobalamins; Vitamin B 12; Vitamin B 12 Deficiency; Vitamin B 6; Vitamin B 6 Deficiency

2006
Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria.
    Molecular genetics and metabolism, 2008, Volume: 94, Issue:1

    Topics: Adolescent; Adult; Body Mass Index; Child; Child, Preschool; Female; Homocysteine; Humans; Hyperhomocysteinemia; Male; Phenylketonurias; Polymorphism, Genetic; Vitamin B 12; Vitamin B 6; Vitamin B Deficiency

2008
Hair amino acids in cystinosis, homocystinuria, Fölling's disease and tyrosinosis.
    Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:3

    Topics: Amino Acids; Autoanalysis; Citrulline; Cystine; Cystinosis; Female; Hair; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Male; Metabolic Diseases; Methionine; Methods; Phenylalanine; Phenylketonurias; Proline; Tyrosine

1969