214 related articles for article (PubMed ID: 19629901)
21. Hereditary hypophosphatasia and hyperphosphatasia.
Silve C
Curr Opin Rheumatol; 1994 May; 6(3):336-9. PubMed ID: 8060771
[TBL] [Abstract][Full Text] [Related]
22. [Hypophosphatasia : What is currently available for treatment?].
Schmidt T; Amling M; Barvencik F
Internist (Berl); 2016 Dec; 57(12):1145-1154. PubMed ID: 27796472
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. How can calcium pyrophosphate crystals induce inflammation in hypophosphatasia or chronic inflammatory joint diseases?
Beck C; Morbach H; Richl P; Stenzel M; Girschick HJ
Rheumatol Int; 2009 Jan; 29(3):229-38. PubMed ID: 18821074
[TBL] [Abstract][Full Text] [Related]
26. [Therapy for hypophosphatasia].
Ozono K
Clin Calcium; 2007 Oct; 17(10):1600-6. PubMed ID: 17906415
[TBL] [Abstract][Full Text] [Related]
27. [Case report on hypophosphatasia (Rathbun's disease)].
Hähnel H
Z Arztl Fortbild (Jena); 1977 Dec; 71(24):1188-92. PubMed ID: 602291
[No Abstract] [Full Text] [Related]
28. Aberrant interchain disulfide bridge of tissue-nonspecific alkaline phosphatase with an Arg433-->Cys substitution associated with severe hypophosphatasia.
Nasu M; Ito M; Ishida Y; Numa N; Komaru K; Nomura S; Oda K
FEBS J; 2006 Dec; 273(24):5612-24. PubMed ID: 17212778
[TBL] [Abstract][Full Text] [Related]
29. A clinical and research protocol for characterizing patients with hypophosphatasia.
Hu CC; King DL; Thomas HF; Simmer JP
Pediatr Dent; 1996; 18(1):17-23. PubMed ID: 8668564
[No Abstract] [Full Text] [Related]
30. Clinical, laboratory, and genetic investigations of hypophosphatasia: support for autosomal dominant inheritance with homozygous lethality.
Eastman JR; Bixler D
J Craniofac Genet Dev Biol; 1983; 3(3):213-34. PubMed ID: 6643650
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Neurosurgical aspects of childhood hypophosphatasia.
Collmann H; Mornet E; Gattenlöhner S; Beck C; Girschick H
Childs Nerv Syst; 2009 Feb; 25(2):217-23. PubMed ID: 18769927
[TBL] [Abstract][Full Text] [Related]
33. [Hypophosphatasia in adults. Apropos of 2 cases].
Wendling D; Cassou M; Guidet M
Rev Rhum Mal Osteoartic; 1985 Jan; 52(1):43-50. PubMed ID: 3992153
[TBL] [Abstract][Full Text] [Related]
34. Adult hypophosphatasia. Current aspects.
Wendling D; Jeannin-Louys L; Kremer P; Fellmann F; Toussirot E; Mornet E
Joint Bone Spine; 2001 Mar; 68(2):120-4. PubMed ID: 11324927
[TBL] [Abstract][Full Text] [Related]
35. Orodental phenotype and genotype findings in all subtypes of hypophosphatasia.
Reibel A; Manière MC; Clauss F; Droz D; Alembik Y; Mornet E; Bloch-Zupan A
Orphanet J Rare Dis; 2009 Feb; 4():6. PubMed ID: 19232125
[TBL] [Abstract][Full Text] [Related]
36. Hypophosphatasia in a child with widened anterior fontanelle: lessons learned from late diagnosis and incorrect treatment.
Mohn A; De Leonibus C; de Giorgis T; Mornet E; Chiarelli F
Acta Paediatr; 2011 Jul; 100(7):e43-6. PubMed ID: 21342251
[TBL] [Abstract][Full Text] [Related]
37. Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?
Utsch B; Brun-Heath I; Staatz G; Gravou-Apostolatou C; Karle S; Jacobs U; Ludwig M; Zenker M; Dörr HG; Rascher W; Mornet E; Dötsch J
Exp Clin Endocrinol Diabetes; 2009 Jan; 117(1):28-33. PubMed ID: 18523927
[TBL] [Abstract][Full Text] [Related]
38. [A novel mutation in infant hypophophatasia: a case report].
Halioui-Louhaïchi S; Ben M'barek S; Ben Hariz M; Ben Farhat L; Briki S; Hendaoui L; Mornet E; Maherzi A
Tunis Med; 2007 May; 85(5):433-6. PubMed ID: 17657935
[TBL] [Abstract][Full Text] [Related]
39. [Fatal congenital hypophosphatasia].
Péter J; Ferenczy I; Görgényi A; Machay T
Orv Hetil; 1972 Jan; 113(5):258-60. PubMed ID: 5058493
[No Abstract] [Full Text] [Related]
40. Lethal and mild hypophosphatasia in half-sibs.
Eastman J; Bixler D
J Craniofac Genet Dev Biol; 1982; 2(1):35-44. PubMed ID: 7130355
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
