235 related articles for article (PubMed ID: 15875439)
1. Hypophosphatasia in Taiwan: report of two cases.
Chou YY; Ou HY; Wu TJ; Tsai SC; Lin SJ; Yu EH
Kaohsiung J Med Sci; 2005 Mar; 21(3):134-7. PubMed ID: 15875439
[TBL] [Abstract][Full Text] [Related]
2. Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene.
Baumgartner-Sigl S; Haberlandt E; Mumm S; Scholl-Bürgi S; Sergi C; Ryan L; Ericson KL; Whyte MP; Högler W
Bone; 2007 Jun; 40(6):1655-61. PubMed ID: 17395561
[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. Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms.
Fallon MD; Teitelbaum SL; Weinstein RS; Goldfischer S; Brown DM; Whyte MP
Medicine (Baltimore); 1984 Jan; 63(1):12-24. PubMed ID: 6690884
[TBL] [Abstract][Full Text] [Related]
5. [Childhood hypophosphatasia: a case report due to a novel mutation].
Draguet C; Gillerot Y; Mornet E
Arch Pediatr; 2004 May; 11(5):440-3. PubMed ID: 15135428
[TBL] [Abstract][Full Text] [Related]
6. [Hypophosphatasia--biochemical and clinical manifestations, molecular genetic principles].
Chandoga I; Futas J; Petrovic R; Chandoga J
Cas Lek Cesk; 2011; 150(10):541-5. PubMed ID: 22132624
[TBL] [Abstract][Full Text] [Related]
7. Adult hypophosphatasia with compound heterozygous p.Phe327Leu missense and c.1559delT frameshift mutations in tissue-nonspecific alkaline phosphatase gene: a case report.
Fukushima K; Kawai-Kowase K; Yonemoto Y; Fujiwara M; Sato H; Sato M; Kubota T; Ozono K; Tamura J
J Med Case Rep; 2019 Apr; 13(1):101. PubMed ID: 31014398
[TBL] [Abstract][Full Text] [Related]
8. [Hypophosphatasia in an adult, with late clinical manifestations (author's transl)].
Paolaggi JB; Job C; Durigon M; Alterescu R; Auquier L
Nouv Presse Med; 1978 Dec; 7(47):4285-9. PubMed ID: 745977
[TBL] [Abstract][Full Text] [Related]
9. Hypophosphatasia.
Rockman-Greenberg C
Pediatr Endocrinol Rev; 2013 Jun; 10 Suppl 2():380-8. PubMed ID: 23858621
[TBL] [Abstract][Full Text] [Related]
10. Hypophosphatasia: diagnostic application of linked DNA markers in the dominantly inherited adult form.
Iqbal SJ; Plaha DS; Linforth GH; Dalgleish R
Clin Sci (Lond); 1999 Jul; 97(1):73-8. PubMed ID: 10369796
[TBL] [Abstract][Full Text] [Related]
11. Isoenzymes of alkaline phosphatase in infantile hypophosphatasia.
Mueller HD; Stinson RA; Mohyuddin F; Milne JK
J Lab Clin Med; 1983 Jul; 102(1):24-30. PubMed ID: 6854132
[TBL] [Abstract][Full Text] [Related]
12. Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.
Mumm S; Jones J; Finnegan P; Henthorn PS; Podgornik MN; Whyte MP
Mol Genet Metab; 2002 Feb; 75(2):143-53. PubMed ID: 11855933
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Osteomalacia with low alkaline phosphatase: a not so rare condition with important consequences.
Belkhouribchia J; Bravenboer B; Meuwissen M; Velkeniers B
BMJ Case Rep; 2016 Jan; 2016():. PubMed ID: 26823351
[TBL] [Abstract][Full Text] [Related]
15. [Bone pain, spontaneous fractures, muscle weakness].
Walger P; Baumgart P; Lehnert H; Vetter H
Schweiz Rundsch Med Prax; 1987 Oct; 76(41):1141-5. PubMed ID: 3671950
[No Abstract] [Full Text] [Related]
16. Chronic multifocal non-bacterial osteomyelitis in hypophosphatasia mimicking malignancy.
Girschick HJ; Mornet E; Beer M; Warmuth-Metz M; Schneider P
BMC Pediatr; 2007 Jan; 7():3. PubMed ID: 17241478
[TBL] [Abstract][Full Text] [Related]
17. Heterogeneity of adult hypophosphatasia. Report of severe and mild cases.
Weinstein RS; Whyte MP
Arch Intern Med; 1981 May; 141(6):727-31. PubMed ID: 7235780
[TBL] [Abstract][Full Text] [Related]
18. Neonatal hypophosphatasia and seizures. A case report.
Smilari P; Romeo DM; Palazzo P; Meli C; Sorge G
Minerva Pediatr; 2005 Oct; 57(5):319-23. PubMed ID: 16205618
[TBL] [Abstract][Full Text] [Related]
19. Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene.
Stoll C; Fischbach M; Terzic J; Alembik Y; Vuillemin MO; Mornet E
Genet Couns; 2002; 13(3):289-95. PubMed ID: 12416636
[TBL] [Abstract][Full Text] [Related]
20. A novel missense mutation of the tissue-nonspecific alkaline phosphatase gene detected in a patient with hypophosphatasia.
Sugimoto N; Iwamoto S; Hoshino Y; Kajii E
J Hum Genet; 1998; 43(3):160-4. PubMed ID: 9747027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
