Page last updated: 2024-09-05

biotin and BH4 Deficiency

biotin has been researched along with BH4 Deficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, J; Chen, SZ; Fan, CH; Li, R; Liu, XM; Sang, Y1
Lee, EB1
Georgala, S; Ithakisios, D; Leondiadis, L; Livaniou, E; Nyalala, JO; Papakonstantinou, ED; Schulpis, KH1
Lowe, JB1

Reviews

2 review(s) available for biotin and BH4 Deficiency

ArticleYear
Metabolic diseases and the skin.
    Pediatric clinics of North America, 1983, Volume: 30, Issue:4

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Biotin; Child; Child, Preschool; Hartnup Disease; Homocystinuria; Humans; Infant; Infant, Newborn; Phenylketonurias; Skin Diseases; Tyrosine; Tyrosine Transaminase

1983
Clinical applications of gene probes in human genetic disease, malignancy, and infectious disease.
    Clinica chimica acta; international journal of clinical chemistry, 1986, May-30, Volume: 157, Issue:1

    Topics: B-Lymphocytes; Bacterial Infections; Biotin; Cloning, Molecular; Deoxyribonucleotides; DNA; DNA Restriction Enzymes; DNA, Recombinant; Female; Genetic Carrier Screening; Genetic Diseases, Inborn; Genotype; Hemophilia A; Humans; Immunoglobulins; Infections; Leukemia, Lymphoid; Leukocytes; Male; Muscular Dystrophies; Nucleic Acid Hybridization; Phenylketonurias; Phosphorus Radioisotopes; Polymorphism, Genetic; Pregnancy; Prenatal Diagnosis; Receptors, Antigen, T-Cell; RNA; T-Lymphocytes; Virus Diseases

1986

Other Studies

2 other study(ies) available for biotin and BH4 Deficiency

ArticleYear
Screening of Inherited Metabolic Disorders in Infants with Infantile Spasms.
    Cell biochemistry and biophysics, 2015, Volume: 72, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Anticonvulsants; Biotin; Brain; Brain Diseases, Metabolic; Chromatography, Gas; Developmental Disabilities; Epilepsy; Female; Glutaryl-CoA Dehydrogenase; Humans; Infant; Liver; Liver Function Tests; Magnetic Resonance Imaging; Male; Mass Screening; Mass Spectrometry; Metabolic Diseases; Phenylketonurias; Spasms, Infantile; Succinate-Semialdehyde Dehydrogenase; Tomography, X-Ray Computed

2015
Biotin recycling impairment in phenylketonuric children with seborrheic dermatitis.
    International journal of dermatology, 1998, Volume: 37, Issue:12

    Topics: Amidohydrolases; Biotin; Biotinidase; Child; Child, Preschool; Dermatitis, Seborrheic; Humans; Phenylalanine; Phenylketonurias

1998