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300 related items for PubMed ID: 26219704
21. Severe perinatal hypophosphatasia case with a novel mutation. Yazici H, Canda E, Kalkan Ucar S, Coker M. Arch Argent Pediatr; 2022 Feb; 120(1):e21-e24. PubMed ID: 35068125 [Abstract] [Full Text] [Related]
26. Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health. Lin EL, Gottesman GS, McAlister WH, Bijanki VN, Mack KE, Griffin DM, Mumm S, Whyte MP. Bone; 2020 Jul; 136():115322. PubMed ID: 32200022 [Abstract] [Full Text] [Related]
27. Physiological role of alkaline phosphatase explored in hypophosphatasia. Whyte MP. Ann N Y Acad Sci; 2010 Mar; 1192():190-200. PubMed ID: 20392236 [Abstract] [Full Text] [Related]
32. Hypophosphatasia in Adults: Clinical Spectrum and Its Association With Genetics and Metabolic Substrates. Lefever E, Witters P, Gielen E, Vanclooster A, Meersseman W, Morava E, Cassiman D, Laurent MR. J Clin Densitom; 2020 May 01; 23(3):340-348. PubMed ID: 30655187 [Abstract] [Full Text] [Related]
34. Pathophysiology of hypophosphatasia and the potential role of asfotase alfa. Orimo H. Ther Clin Risk Manag; 2016 May 01; 12():777-86. PubMed ID: 27274262 [Abstract] [Full Text] [Related]
35. Tissue-Nonspecific Alkaline Phosphatase-A Gatekeeper of Physiological Conditions in Health and a Modulator of Biological Environments in Disease. Liedtke D, Hofmann C, Jakob F, Klopocki E, Graser S. Biomolecules; 2020 Dec 08; 10(12):. PubMed ID: 33302551 [Abstract] [Full Text] [Related]
36. Rare diseases: a challenge in paediatric dentistry. Giuca MR. Eur J Paediatr Dent; 2024 Sep 03; 25(3):171-171. PubMed ID: 39212455 [Abstract] [Full Text] [Related]
37. Enzyme replacement therapy for murine hypophosphatasia. Millán JL, Narisawa S, Lemire I, Loisel TP, Boileau G, Leonard P, Gramatikova S, Terkeltaub R, Camacho NP, McKee MD, Crine P, Whyte MP. J Bone Miner Res; 2008 Jun 03; 23(6):777-87. PubMed ID: 18086009 [Abstract] [Full Text] [Related]
38. Enzyme replacement therapy for congenital hypophosphatasia allows for surgical treatment of related complex craniosynostosis: a case series. Kosnik-Infinger L, Gendron C, Gordon CB, Pan BS, van Aalst JA, Vogel TW. Neurosurg Focus; 2015 May 03; 38(5):E10. PubMed ID: 25929963 [Abstract] [Full Text] [Related]
39. Neuromuscular features of hypophosphatasia. Fonta C, Salles JP. Arch Pediatr; 2017 May 03; 24(5S2):5S85-5S88. PubMed ID: 29405939 [Abstract] [Full Text] [Related]
40. Infantile hypophosphatasia combined with vitamin B6-responsive seizures and reticular formation lesions on magnetic resonance imaging: A case report. Fukazawa M, Tezuka J, Sasazuki M, Masumoto N, Baba H, Doi T, Tsutsumi Y, Mizuno Y, Mihara F, Nakayama H. Brain Dev; 2018 Feb 03; 40(2):140-144. PubMed ID: 28802630 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]