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Journal Abstract Search

300 related items for PubMed ID: 26219704

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  • 12. Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patients.
    Whyte MP, Zhang F, Wenkert D, McAlister WH, Mack KE, Benigno MC, Coburn SP, Wagy S, Griffin DM, Ericson KL, Mumm S.
    Bone; 2015 Jun; 75():229-39. PubMed ID: 25731960
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  • 13. Pediatric hypophosphatasia: avoid diagnosis missteps!
    Whyte MP, McAlister WH, Mack KE, Mumm S, Madson KL.
    J Bone Miner Res; 2024 Jul 23; 39(6):655-660. PubMed ID: 38905292
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  • 15. Neurological Symptoms of Hypophosphatasia.
    Taketani T.
    Subcell Biochem; 2015 Jul 23; 76():309-22. PubMed ID: 26219717
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  • 16. Improvement of the skeletal and dental hypophosphatasia phenotype in Alpl-/- mice by administration of soluble (non-targeted) chimeric alkaline phosphatase.
    Gasque KC, Foster BL, Kuss P, Yadav MC, Liu J, Kiffer-Moreira T, van Elsas A, Hatch N, Somerman MJ, Millán JL.
    Bone; 2015 Mar 23; 72():137-47. PubMed ID: 25433339
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  • 17. Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.
    Akiyama T, Kubota T, Ozono K, Michigami T, Kobayashi D, Takeyari S, Sugiyama Y, Noda M, Harada D, Namba N, Suzuki A, Utoyama M, Kitanaka S, Uematsu M, Mitani Y, Matsunami K, Takishima S, Ogawa E, Kobayashi K.
    Mol Genet Metab; 2018 Sep 23; 125(1-2):174-180. PubMed ID: 30049651
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  • 18. Compound heterozygosity of two functional null mutations in the ALPL gene associated with deleterious neurological outcome in an infant with hypophosphatasia.
    Hofmann C, Liese J, Schwarz T, Kunzmann S, Wirbelauer J, Nowak J, Hamann J, Girschick H, Graser S, Dietz K, Zeck S, Jakob F, Mentrup B.
    Bone; 2013 Jul 23; 55(1):150-7. PubMed ID: 23454488
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  • 20. Molecular Genetics of Hypophosphatasia and Phenotype-Genotype Correlations.
    Mornet E.
    Subcell Biochem; 2015 Jul 23; 76():25-43. PubMed ID: 26219705
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