These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. 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 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
18. [Hypophosphatasia]. Tsiantouli E, Trombetti A, Ferrari S. Rev Med Suisse; 2017 Apr 19; 13(559):855-858. PubMed ID: 28727343 [Abstract] [Full Text] [Related]
19. Safety, pharmacokinetics, and pharmacodynamics of efzimfotase alfa, a second-generation enzyme replacement therapy: phase 1, dose-escalation study in adults with hypophosphatasia. Dahir KM, Shannon A, Dunn D, Voegtli W, Dong Q, Hasan J, Pradhan R, Pelto R, Pan WJ. J Bone Miner Res; 2024 Sep 26; 39(10):1412-1423. PubMed ID: 39135540 [Abstract] [Full Text] [Related]
20. Recurrent Metatarsal Fractures in Postmenopausal Woman With Low Serum Alkaline Phosphatase: A Rare Diagnosis Not to Miss. Iqbal U, Anwar H, Chaudhary A, Alvi M, Freeth A. J Investig Med High Impact Case Rep; 2017 Sep 26; 5(3):2324709617718851. PubMed ID: 28748194 [Abstract] [Full Text] [Related] Page: [Next] [New Search]