Kovach MJ - Search Results

1

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone.

Kimonis VE, Kovach MJ, Waggoner B, Leal S, Salam A, Rimer L, Davis K, Khardori R, Gelber D. Kimonis VE, et al. Among authors: kovach mj. Genet Med. 2000 Jul-Aug;2(4):232-41. doi: 10.1097/00125817-200007000-00006. Genet Med. 2000. PMID: 11252708 Free PMC article.

2

Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.

Waggoner B, Kovach MJ, Winkelman M, Cai D, Khardori R, Gelber D, Kimonis VE. Waggoner B, et al. Among authors: kovach mj. Am J Med Genet. 2002 Mar 15;108(3):187-91. doi: 10.1002/ajmg.10199. Am J Med Genet. 2002. PMID: 11891683

3

A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.

Kovach MJ, Lin JP, Boyadjiev S, Campbell K, Mazzeo L, Herman K, Rimer LA, Frank W, Llewellyn B, Jabs EW, Gelber D, Kimonis VE. Kovach MJ, et al. Am J Hum Genet. 1999 Jun;64(6):1580-93. doi: 10.1086/302420. Am J Hum Genet. 1999. PMID: 10330345 Free PMC article.

4

Genetic heterogeneity in autosomal dominant essential tremor.

Kovach MJ, Ruiz J, Kimonis K, Mueed S, Sinha S, Higgins C, Elble S, Elble R, Kimonis VE. Kovach MJ, et al. Genet Med. 2001 May-Jun;3(3):197-9. doi: 10.1097/00125817-200105000-00009. Genet Med. 2001. PMID: 11388761 Free article.

5

Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families.

Chen AS, Kovach MJ, Herman K, Avakian A, Frank W, Forrester S, Lin JP, Kimonis V. Chen AS, et al. Among authors: kovach mj. Genet Med. 2000 Sep-Oct;2(5):283-9. doi: 10.1097/00125817-200009000-00003. Genet Med. 2000. PMID: 11399209 Free article.

6

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

Kovach MJ, Waggoner B, Leal SM, Gelber D, Khardori R, Levenstien MA, Shanks CA, Gregg G, Al-Lozi MT, Miller T, Rakowicz W, Lopate G, Florence J, Glosser G, Simmons Z, Morris JC, Whyte MP, Pestronk A, Kimonis VE. Kovach MJ, et al. Mol Genet Metab. 2001 Dec;74(4):458-75. doi: 10.1006/mgme.2001.3256. Mol Genet Metab. 2001. PMID: 11749051 Free PMC article.

7

Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature.

Kovach MJ, Campbell KC, Herman K, Waggoner B, Gelber D, Hughes LF, Kimonis VE. Kovach MJ, et al. Am J Med Genet. 2002 Apr 1;108(4):295-303. doi: 10.1002/ajmg.10223. Am J Med Genet. 2002. PMID: 11920834 Review.

8

Kousseff syndrome caused by deletion of chromosome 22q11-13.

Forrester S, Kovach MJ, Smith RE, Rimer L, Wesson M, Kimonis VE. Forrester S, et al. Among authors: kovach mj. Am J Med Genet. 2002 Nov 1;112(4):338-42. doi: 10.1002/ajmg.10625. Am J Med Genet. 2002. PMID: 12376934

9

Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.

Forrester S, Kovach MJ, Reynolds NM, Urban R, Kimonis V. Forrester S, et al. Among authors: kovach mj. Am J Med Genet. 2001 Jan 1;98(1):92-100. Am J Med Genet. 2001. PMID: 11426460 Free article. Review.

10

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: kovach mj. Nat Genet. 2004 Apr;36(4):377-81. doi: 10.1038/ng1332. Epub 2004 Mar 21. Nat Genet. 2004. PMID: 15034582 Free article.

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