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Journal Abstract Search

326 related items for PubMed ID: 31400546

  • 1. Molecular and cellular basis of hypophosphatasia.
    Komaru K, Ishida-Okumura Y, Numa-Kinjoh N, Hasegawa T, Oda K.
    J Oral Biosci; 2019 Sep; 61(3):141-148. PubMed ID: 31400546
    [Abstract] [Full Text] [Related]

  • 2. [Tissue-nonspecific alkaline phosphatase and hypophosphatasia].
    Oda K, Kinjoh NN, Sohda M, Komaru K, Amizuka N.
    Clin Calcium; 2014 Feb; 24(2):233-9. PubMed ID: 24473356
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  • 3. Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.
    Glotov OS, Savostyanov KV, Nagornova TS, Chernov AN, Fedyakov MA, Raspopova AN, Krasnoukhov KN, Danilov LG, Moiseeva NV, Kalinin RS, Tsai VV, Eismont YA, Voinova VY, Vitebskaya AV, Gurkina EY, Kuzenkova LM, Sosnina IB, Pushkov AA, Zhanin IS, Zakharova EY.
    Int J Mol Sci; 2022 Oct 26; 23(21):. PubMed ID: 36361766
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  • 4. Hypophosphatasia: Biochemical hallmarks validate the expanded pediatric clinical nosology.
    Whyte MP, Coburn SP, Ryan LM, Ericson KL, Zhang F.
    Bone; 2018 May 26; 110():96-106. PubMed ID: 29360619
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  • 5. Hypophosphatasia: An overview For 2017.
    Whyte MP.
    Bone; 2017 Sep 26; 102():15-25. PubMed ID: 28238808
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  • 6. Alkaline Phosphatase Replacement Therapy for Hypophosphatasia in Development and Practice.
    Bowden SA, Foster BL.
    Adv Exp Med Biol; 2019 Sep 26; 1148():279-322. PubMed ID: 31482504
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  • 12. A novel combination of biallelic ALPL mutations associated with adult hypophosphatasia: A phenotype-genotype association and computational analysis study.
    Martins L, de Almeida AB, Dos Santos EJL, Foster BL, Machado RA, Kantovitz KR, Coletta RD, Nociti FH.
    Bone; 2019 Aug 26; 125():128-139. PubMed ID: 31077853
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  • 13. Molecular defect of tissue-nonspecific alkaline phosphatase bearing a substitution at position 426 associated with hypophosphatasia.
    Al-Shawafi HA, Komaru K, Oda K.
    Mol Cell Biochem; 2017 Mar 26; 427(1-2):169-176. PubMed ID: 28000043
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  • 15. Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review.
    Mao X, Liu S, Lin Y, Chen Z, Shao Y, Yu Q, Liu H, Lu Z, Sheng H, Lu X, Huang Y, Liu L, Zeng C.
    BMC Pediatr; 2019 Nov 25; 19(1):456. PubMed ID: 31760938
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