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Items: 1 to 20 of 22

1.

Asfotase alfa therapy for children with hypophosphatasia.

Whyte MP, Madson KL, Phillips D, Reeves AL, McAlister WH, Yakimoski A, Mack KE, Hamilton K, Kagan K, Fujita KP, Thompson DD, Moseley S, Odrljin T, Rockman-Greenberg C.

JCI Insight. 2016 Jun 16;1(9):e85971.

2.

Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease.

Gottesman GS, Madson KL, McAlister WH, Nenninger A, Wenkert D, Mumm S, Whyte MP.

Am J Med Genet A. 2016 Apr;170A(4):978-85. doi: 10.1002/ajmg.a.37536. Epub 2016 Jan 14. Review.

3.

Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic Mastocytosis.

Whyte MP, Madson KL, McAlister WH, Mumm S, Novack DV, Blair JC, Shaw NJ.

J Bone Miner Res. 2015 Aug;30(8):1537. doi: 10.1002/jbmr.2561. Epub 2015 Jun 10. No abstract available.

4.

Response to: A rapid skeletal turnover in radiographic mimic of osteopetrosis might be secondary to systemic mastocytosis.

Whyte MP, Madson KL, McAlister WH, Mumm S, Novack DV, Blair JC, Shaw NJ.

J Bone Miner Res. 2015 May;30(5):946. doi: 10.1002/jbmr.2455. No abstract available. Erratum in: J Bone Miner Res. 2015 Aug;30(8):1537.

5.

PHEX 3'-UTR c.*231A>G near the polyadenylation signal is a relatively common, mild, American mutation that masquerades as sporadic or X-linked recessive hypophosphatemic rickets.

Mumm S, Huskey M, Cajic A, Wollberg V, Zhang F, Madson KL, Wenkert D, McAlister WH, Gottesman GS, Whyte MP.

J Bone Miner Res. 2015 Jan;30(1):137-43. doi: 10.1002/jbmr.2307.

6.

Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.

Mumm S, Huskey M, Duan S, Wenkert D, Madson KL, Gottesman GS, Nenninger AR, Laxer RM, McAlister WH, Whyte MP.

Am J Med Genet A. 2014 Sep;164A(9):2287-93. doi: 10.1002/ajmg.a.36641. Epub 2014 Jul 2.

7.

Rapid skeletal turnover in a radiographic mimic of osteopetrosis.

Whyte MP, Madson KL, Mumm S, McAlister WH, Novack DV, Blair JC, Helliwell TR, Stolina M, Abernethy LJ, Shaw NJ.

J Bone Miner Res. 2014 Dec;29(12):2601-9. doi: 10.1002/jbmr.2289.

8.

Early illness features associated with mortality in the juvenile idiopathic inflammatory myopathies.

Huber AM, Mamyrova G, Lachenbruch PA, Lee JA, Katz JD, Targoff IN, Miller FW, Rider LG; Childhood Myositis Heterogeneity Collaborative Study Group.

Arthritis Care Res (Hoboken). 2014 May;66(5):732-40. doi: 10.1002/acr.22212.

9.

The myositis autoantibody phenotypes of the juvenile idiopathic inflammatory myopathies.

Rider LG, Shah M, Mamyrova G, Huber AM, Rice MM, Targoff IN, Miller FW; Childhood Myositis Heterogeneity Collaborative Study Group.

Medicine (Baltimore). 2013 Jul;92(4):223-43. doi: 10.1097/MD.0b013e31829d08f9.

10.

The clinical phenotypes of the juvenile idiopathic inflammatory myopathies.

Shah M, Mamyrova G, Targoff IN, Huber AM, Malley JD, Rice MM, Miller FW, Rider LG; Childhood Myositis Heterogeneity Collaborative Study Group.

Medicine (Baltimore). 2013 Jan;92(1):25-41. doi: 10.1097/MD.0b013e31827f264d.

11.

Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy.

Otero JE, Gottesman GS, McAlister WH, Mumm S, Madson KL, Kiffer-Moreira T, Sheen C, Millán JL, Ericson KL, Whyte MP.

J Bone Miner Res. 2013 Feb;28(2):419-30. doi: 10.1002/jbmr.1752.

12.

Environmental factors preceding illness onset differ in phenotypes of the juvenile idiopathic inflammatory myopathies.

Rider LG, Wu L, Mamyrova G, Targoff IN, Miller FW; Childhood Myositis Heterogeneity Collaborative Study Group.

Rheumatology (Oxford). 2010 Dec;49(12):2381-90. doi: 10.1093/rheumatology/keq277. Epub 2010 Aug 27.

13.

Cytokine gene polymorphisms as risk and severity factors for juvenile dermatomyositis.

Mamyrova G, O'Hanlon TP, Sillers L, Malley K, James-Newton L, Parks CG, Cooper GS, Pandey JP, Miller FW, Rider LG; Childhood Myositis Heterogeneity Collaborative Study Group.

Arthritis Rheum. 2008 Dec;58(12):3941-50. doi: 10.1002/art.24039.

14.

Daily hassles and social support as predictors of adjustment in children with pediatric rheumatic disease.

von Weiss RT, Rapoff MA, Varni JW, Lindsley CB, Olson NY, Madson KL, Bernstein BH.

J Pediatr Psychol. 2002 Mar;27(2):155-65.

PMID:
11821499
15.

Cytokine levels in serum and synovial fluid of patients with juvenile rheumatoid arthritis.

Madson KL, Moore TL, Lawrence JM 3rd, Osborn TG.

J Rheumatol. 1994 Dec;21(12):2359-63.

PMID:
7699643
16.

Arthropathies of cystic fibrosis: case reports and review of the literature.

Lawrence JM 3rd, Moore TL, Madson KL, Rejent AJ, Osborn TG.

J Rheumatol Suppl. 1993 Jul;38:12-5. Review.

PMID:
8366507
17.

Autoantibody studies in juvenile rheumatoid arthritis.

Lawrence JM 3rd, Moore TL, Osborn TG, Nesher G, Madson KL, Kinsella MB.

Semin Arthritis Rheum. 1993 Feb;22(4):265-74. Review.

PMID:
8484133
18.

Interactions between autonomic nerves and endocrine cells of the gastroenteropancreatic system.

Smith PH, Madson KL.

Diabetologia. 1981 Mar;20(Suppl 1):314-324.

PMID:
27942817
19.

Interactions between autonomic nerves and endocrine cells of the gastroenteropancreatic system.

Smith PH, Madson KL.

Diabetologia. 1981 Mar;20 Suppl:314-24. Review.

PMID:
6262172

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