Coburn SP - Search Results

1

Hypophosphatasia: Biochemical hallmarks validate the expanded pediatric clinical nosology.

Whyte MP, Coburn SP, Ryan LM, Ericson KL, Zhang F. Whyte MP, et al. Among authors: coburn sp. Bone. 2018 May;110:96-106. doi: 10.1016/j.bone.2018.01.022. Epub 2018 Jan 31. Bone. 2018. PMID: 29360619

2

Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia.

Whyte MP, Wenkert D, McAlister WH, Mughal MZ, Freemont AJ, Whitehouse R, Baildam EM, Coburn SP, Ryan LM, Mumm S. Whyte MP, et al. Among authors: coburn sp. J Bone Miner Res. 2009 Aug;24(8):1493-505. doi: 10.1359/jbmr.090308. J Bone Miner Res. 2009. PMID: 19335222 Free article.

3

Hypophosphatasia: nonlethal disease despite skeletal presentation in utero (17 new cases and literature review).

Wenkert D, McAlister WH, Coburn SP, Zerega JA, Ryan LM, Ericson KL, Hersh JH, Mumm S, Whyte MP. Wenkert D, et al. Among authors: coburn sp. J Bone Miner Res. 2011 Oct;26(10):2389-98. doi: 10.1002/jbmr.454. J Bone Miner Res. 2011. PMID: 21713987 Free article. Review.

4

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. Whyte MP, et al. Among authors: coburn sp. Bone. 2015 Jun;75:229-39. doi: 10.1016/j.bone.2015.02.022. Epub 2015 Feb 27. Bone. 2015. PMID: 25731960

5

Vitamin B₆ deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasia.

Whyte MP, May JD, McAlister WH, Burgener K, Cortez SR, Kreienkamp R, Castro O, Verzola R, Zavala AS, McPherson CC, Gottesman GS, Ericson KL, Coburn SP, Arbelaez AM. Whyte MP, et al. Among authors: coburn sp. Bone. 2021 Sep;150:116007. doi: 10.1016/j.bone.2021.116007. Epub 2021 May 14. Bone. 2021. PMID: 34000433

6

Hypophosphatasia: Vitamin B₆ status of affected children and adults.

Whyte MP, Zhang F, Wenkert D, Mack KE, Bijanki VN, Ericson KL, Coburn SP. Whyte MP, et al. Among authors: coburn sp. Bone. 2022 Jan;154:116204. doi: 10.1016/j.bone.2021.116204. Epub 2021 Sep 20. Bone. 2022. PMID: 34547524

7

Marrow cell transplantation for infantile hypophosphatasia.

Whyte MP, Kurtzberg J, McAlister WH, Mumm S, Podgornik MN, Coburn SP, Ryan LM, Miller CR, Gottesman GS, Smith AK, Douville J, Waters-Pick B, Armstrong RD, Martin PL. Whyte MP, et al. Among authors: coburn sp. J Bone Miner Res. 2003 Apr;18(4):624-36. doi: 10.1359/jbmr.2003.18.4.624. J Bone Miner Res. 2003. PMID: 12674323 Free article.

8

Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia.

Fedde KN, Blair L, Silverstein J, Coburn SP, Ryan LM, Weinstein RS, Waymire K, Narisawa S, Millán JL, MacGregor GR, Whyte MP. Fedde KN, et al. Among authors: coburn sp. J Bone Miner Res. 1999 Dec;14(12):2015-26. doi: 10.1359/jbmr.1999.14.12.2015. J Bone Miner Res. 1999. PMID: 10620060 Free PMC article.

9

Elevated plasma 4-pyridoxic acid in renal insufficiency.

Coburn SP, Reynolds RD, Mahuren JD, Schaltenbrand WE, Wang Y, Ericson KL, Whyte MP, Zubovic YM, Ziegler PJ, Costill DL, Fink WJ, Pearson DR, Pauly TA, Thampy KG, Wortsman J. Coburn SP, et al. Am J Clin Nutr. 2002 Jan;75(1):57-64. doi: 10.1093/ajcn/75.1.57. Am J Clin Nutr. 2002. PMID: 11756060 Clinical Trial.

10

Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement.

Stevenson DA, Carey JC, Coburn SP, Ericson KL, Byrne JL, Mumm S, Whyte MP. Stevenson DA, et al. Among authors: coburn sp. J Clin Endocrinol Metab. 2008 Sep;93(9):3443-8. doi: 10.1210/jc.2008-0318. Epub 2008 Jun 17. J Clin Endocrinol Metab. 2008. PMID: 18559907 Free PMC article.

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