BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

442 related articles for article (PubMed ID: 17916236)

  • 1. Hypophosphatasia.
    Mornet E
    Orphanet J Rare Dis; 2007 Oct; 2():40. PubMed ID: 17916236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypophosphatasia.
    Mornet E
    Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):113-27. PubMed ID: 18328985
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Congenital hypophosphatasia].
    Terheggen HG; Wischermann A
    Monatsschr Kinderheilkd; 1984 Jul; 132(7):512-22. PubMed ID: 6147751
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia.
    Tenorio J; Álvarez I; Riancho-Zarrabeitia L; Martos-Moreno GÁ; Mandrile G; de la Flor Crespo M; Sukchev M; Sherif M; Kramer I; Darnaude-Ortiz MT; Arias P; Gordo G; Dapía I; Martinez-Villanueva J; Gómez R; Iturzaeta JM; Otaify G; García-Unzueta M; Rubinacci A; Riancho JA; Aglan M; Temtamy S; Hamid MA; Argente J; Ruiz-Pérez VL; Heath KE; Lapunzina P
    Am J Med Genet A; 2017 Mar; 173(3):601-610. PubMed ID: 28127875
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 19(1):456. PubMed ID: 31760938
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Utility of genetic testing for prenatal presentations of hypophosphatasia.
    Sperelakis-Beedham B; Taillandier A; Domingues C; Guberto M; Colin E; Porquet-Bordes V; Rothenbuhler A; Salles JP; Wenkert D; Zankl A; Muti C; Bacrot S; Simon-Bouy B; Mornet E
    Mol Genet Metab; 2021 Mar; 132(3):198-203. PubMed ID: 33549410
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Childhood hypophosphatasia].
    Mulder AL; van den Bos SN; Gerrits GP; Theunissen PM
    Ned Tijdschr Geneeskd; 1997 Jul; 141(27):1345-8. PubMed ID: 9380189
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical Forms and Animal Models of Hypophosphatasia.
    Salles JP
    Subcell Biochem; 2015; 76():3-24. PubMed ID: 26219704
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypophosphatasia.
    Fenn JS; Lorde N; Ward JM; Borovickova I
    J Clin Pathol; 2021 Oct; 74(10):635-640. PubMed ID: 33931563
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypophosphatasia: an overview of the disease and its treatment.
    Bianchi ML
    Osteoporos Int; 2015 Dec; 26(12):2743-57. PubMed ID: 26245849
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Treatment of hypophosphatasia.
    Simon S; Resch H
    Wien Med Wochenschr; 2020 Apr; 170(5-6):112-115. PubMed ID: 32072352
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetics of hypophosphatasia].
    Mornet E; Simon-Bouy B
    Arch Pediatr; 2004 May; 11(5):444-8. PubMed ID: 15135429
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia.
    Haliloglu B; Guran T; Atay Z; Abali S; Mornet E; Bereket A; Turan S
    Eur J Pediatr; 2013 Jun; 172(6):851-3. PubMed ID: 23093139
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetics of hypophosphatasia.
    Mornet E
    Arch Pediatr; 2017 May; 24(5S2):5S51-5S56. PubMed ID: 29405932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypophosphatasia.
    Mornet E
    Metabolism; 2018 May; 82():142-155. PubMed ID: 28939177
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prosthetic rehabilitation of hypophosphatasia: a case report.
    Bağiş B; Baltacioğlu E; Aydoğan E; Tamam E
    Cases J; 2008 Dec; 2():7626. PubMed ID: 19918476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review.
    Park EG; Cho SY; Lee J; Kim J; Cho H; Kim J; Huh R; Ki CS; Kim OH; Jin DK
    Ann Clin Lab Sci; 2016 May; 46(3):302-7. PubMed ID: 27312557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL gene.
    Spentchian M; Merrien Y; Herasse M; Dobbie Z; Gläser D; Holder SE; Ivarsson SA; Kostiner D; Mansour S; Norman A; Roth J; Stipoljev F; Taillemite JL; van der Smagt JJ; Serre JL; Simon-Bouy B; Taillandier A; Mornet E
    Hum Mutat; 2003 Jul; 22(1):105-6. PubMed ID: 12815606
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lethal perinatal hypophosphatasia caused by a novel compound heterozygous mutation: a case report.
    Yu F; Wang J; Xu X
    BMC Pediatr; 2019 Apr; 19(1):109. PubMed ID: 30979366
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 23.