Whyte MP - Search Results

1

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Watts GD, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, Pestronk A, Whyte MP, Kimonis VE. Watts GD, et al. Among authors: whyte mp. Nat Genet. 2004 Apr;36(4):377-81. doi: 10.1038/ng1332. Epub 2004 Mar 21. Nat Genet. 2004. PMID: 15034582 Free article.

2

mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Mumm S, Whyte MP, Thakker RV, Buetow KH, Schlessinger D. Mumm S, et al. Among authors: whyte mp. Am J Hum Genet. 1997 Jan;60(1):153-9. Am J Hum Genet. 1997. PMID: 8981958 Free PMC article.

3

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Trump D, Dixon PH, Mumm S, Wooding C, Davies KE, Schlessinger D, Whyte MP, Thakker RV. Trump D, et al. Among authors: whyte mp. J Med Genet. 1998 Nov;35(11):905-9. doi: 10.1136/jmg.35.11.905. J Med Genet. 1998. PMID: 9832036 Free PMC article.

4

A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.

Mumm S, Christie PT, Finnegan P, Jones J, Dixon PH, Pannett AA, Harding B, Gottesman GS, Thakker RV, Whyte MP. Mumm S, et al. Among authors: whyte mp. J Clin Endocrinol Metab. 2000 Sep;85(9):3343-7. doi: 10.1210/jcem.85.9.6840. J Clin Endocrinol Metab. 2000. PMID: 10999831 Clinical Trial.

5

Hypophosphatasia: molecular diagnosis of Rathbun's original case.

Mumm S, Jones J, Finnegan P, Whyte MP. Mumm S, et al. Among authors: whyte mp. J Bone Miner Res. 2001 Sep;16(9):1724-7. doi: 10.1359/jbmr.2001.16.9.1724. J Bone Miner Res. 2001. PMID: 11547844 Free article.

6

Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin.

Mumm S, Zhang X, Gottesman GS, McAlister WH, Whyte MP. Mumm S, et al. Among authors: whyte mp. J Bone Miner Res. 2001 Dec;16(12):2245-50. doi: 10.1359/jbmr.2001.16.12.2245. J Bone Miner Res. 2001. PMID: 11760838 Free article.

7

Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.

Mumm S, Jones J, Finnegan P, Henthorn PS, Podgornik MN, Whyte MP. Mumm S, et al. Among authors: whyte mp. Mol Genet Metab. 2002 Feb;75(2):143-53. doi: 10.1006/mgme.2001.3283. Mol Genet Metab. 2002. PMID: 11855933

8

Osteoprotegerin deficiency and juvenile Paget's disease.

Whyte MP, Obrecht SE, Finnegan PM, Jones JL, Podgornik MN, McAlister WH, Mumm S. Whyte MP, et al. N Engl J Med. 2002 Jul 18;347(3):175-84. doi: 10.1056/NEJMoa013096. N Engl J Med. 2002. PMID: 12124406 Free article.

9

Bisphosphonate-induced osteopetrosis.

Whyte MP, Wenkert D, Clements KL, McAlister WH, Mumm S. Whyte MP, et al. N Engl J Med. 2003 Jul 31;349(5):457-63. doi: 10.1056/NEJMoa023110. N Engl J Med. 2003. PMID: 12890844 Free article. No abstract available.

10

High-bone-mass disease and LRP5.

Whyte MP, Reinus WH, Mumm S. Whyte MP, et al. N Engl J Med. 2004 May 13;350(20):2096-9; author reply 2096-9. doi: 10.1056/NEJM200405133502017. N Engl J Med. 2004. PMID: 15141052 No abstract available.

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