Compounds > biotin
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biotin and Decreased Muscle Tone

biotin has been researched along with Decreased Muscle Tone in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Bennaoui, F; El Idrissi Slitine, N; El Moussaoui, S; Houcar, O; Maoulainine, FMR1
Creemers, JW; de Zegher, F; Derua, R; Eyskens, F; Francois, I; Jaeken, J; Lecointre, C; Martens, K; Matthijs, G; Meulemans, S; Slootstra, JW; Waelkens, E1
Dimauro, S; Hirano, M; Kanki, T; López, LC; Naini, A; Quinzii, CM; Rodenburg, RJ; Schuelke, M1
Bartlett, K; Charles, BM; Green, A; Hosking, G; Pollitt, R; Taitz, LS1
Frasch, W; Junker, A; Lehnert, W; Niederhoff, H; Saule, H1
Bannwart, C; Baumgartner, R; Suormala, T; Weismann, UN; Wermuth, B1

Other Studies

6 other study(ies) available for biotin and Decreased Muscle Tone

ArticleYear
Biotinidase deficiency in a newborn.
    Journal of neonatal-perinatal medicine, 2020, Volume: 13, Issue:1

    Topics: Age of Onset; Alopecia; Biotin; Biotinidase Deficiency; Consanguinity; Dermatitis, Exfoliative; Eyebrows; Fatal Outcome; Health Services Accessibility; Humans; Ichthyosis; Infant, Newborn; Intensive Care Units, Neonatal; Male; Morocco; Muscle Hypotonia; Myoclonus; Rare Diseases; Vitamin B Complex

2020
Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome.
    American journal of human genetics, 2006, Volume: 78, Issue:1

    Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Base Sequence; Biotin; Blotting, Northern; Chromosomes, Human, Pair 2; Cystinuria; Electrophoresis, Polyacrylamide Gel; Gene Deletion; Genes, Recessive; Humans; Immunohistochemistry; Infant; Infant, Newborn; Molecular Sequence Data; Muscle Hypotonia; Mutagenesis, Site-Directed; Organophosphorus Compounds; Prolyl Oligopeptidases; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Serine Endopeptidases; Substrate Specificity; Syndrome

2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations.
    American journal of human genetics, 2006, Volume: 79, Issue:6

    Topics: Alkyl and Aryl Transferases; Biotin; Carnitine; Case-Control Studies; Cells, Cultured; Coenzymes; Fibroblasts; Humans; Infant; Kidney Diseases; Leigh Disease; Muscle Hypotonia; Mutation; Protein Subunits; Riboflavin; Thiamine; Ubiquinone

2006
Biotin-responsive alopecia and developmental regression.
    Lancet (London, England), 1979, Jul-21, Volume: 2, Issue:8134

    Topics: Alopecia; Biotin; Carbon Dioxide; Crotonates; Dermatitis; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Muscle Hypotonia

1979
A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria.
    European journal of pediatrics, 1979, Volume: 132, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Female; Humans; Infant; Leucine; Muscle Hypotonia; Seizures

1979
Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome.
    Journal of inherited metabolic disease, 1992, Volume: 15, Issue:6

    Topics: Amnion; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Diet Therapy; Fibroblasts; Humans; Infant, Newborn; Ligases; Male; Methylmalonyl-CoA Decarboxylase; Mitochondria; Muscle Hypotonia; Pyruvate Carboxylase; Seizures

1992