Crowe CA - Search Results

1

Cardiac and pulmonary function variability in Duchenne/Becker muscular dystrophy: an initial report.

Birnkrant DJ, Ashwath ML, Noritz GH, Merrill MC, Shah TA, Crowe CA, Bahler RC. Birnkrant DJ, et al. Among authors: crowe ca. J Child Neurol. 2010 Sep;25(9):1110-5. doi: 10.1177/0883073810371003. Epub 2010 May 25. J Child Neurol. 2010. PMID: 20501885 Free PMC article.

2

Left ventricular dysfunction in duchenne muscular dystrophy and genotype.

Ashwath ML, Jacobs IB, Crowe CA, Ashwath RC, Super DM, Bahler RC. Ashwath ML, et al. Among authors: crowe ca. Am J Cardiol. 2014 Jul 15;114(2):284-9. doi: 10.1016/j.amjcard.2014.04.038. Epub 2014 May 2. Am J Cardiol. 2014. PMID: 24878125 Free PMC article.

3

Regional genomic instability predisposes to complex dystrophin gene rearrangements.

Oshima J, Magner DB, Lee JA, Breman AM, Schmitt ES, White LD, Crowe CA, Merrill M, Jayakar P, Rajadhyaksha A, Eng CM, del Gaudio D. Oshima J, et al. Among authors: crowe ca. Hum Genet. 2009 Sep;126(3):411-23. doi: 10.1007/s00439-009-0679-9. Epub 2009 May 16. Hum Genet. 2009. PMID: 19449031

4

Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.

Brown CA, Lanning RW, McKinney KQ, Salvino AR, Cherniske E, Crowe CA, Darras BT, Gominak S, Greenberg CR, Grosmann C, Heydemann P, Mendell JR, Pober BR, Sasaki T, Shapiro F, Simpson DA, Suchowersky O, Spence JE. Brown CA, et al. Among authors: crowe ca. Am J Med Genet. 2001 Sep 1;102(4):359-67. doi: 10.1002/ajmg.1463. Am J Med Genet. 2001. PMID: 11503164

5

Duplication of the pituitary gland associated with multiple blastogenesis defects: Duplication of the pituitary gland (DPG)-plus syndrome. Case report and review of literature.

Manjila S, Miller EA, Vadera S, Goel RK, Khan FR, Crowe C, Geertman RT. Manjila S, et al. Surg Neurol Int. 2012;3:23. doi: 10.4103/2152-7806.92939. Epub 2012 Feb 15. Surg Neurol Int. 2012. PMID: 22439114 Free PMC article.

6

Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype.

Scacheri PC, Gillanders EM, Subramony SH, Vedanarayanan V, Crowe CA, Thakore N, Bingler M, Hoffman EP. Scacheri PC, et al. Among authors: crowe ca. Neurology. 2002 Feb 26;58(4):593-602. doi: 10.1212/wnl.58.4.593. Neurology. 2002. PMID: 11865138

7

Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.

Tay SK, Shanske S, Crowe C, Shanske A, Schafer I, Pancrudo J, Lu J, Bonilla E, DiMauro S. Tay SK, et al. J Child Neurol. 2005 Feb;20(2):142-6. doi: 10.1177/08830738050200022301. J Child Neurol. 2005. PMID: 15794182

8

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease.

Pitceathly RD, Murphy SM, Cottenie E, Chalasani A, Sweeney MG, Woodward C, Mudanohwo EE, Hargreaves I, Heales S, Land J, Holton JL, Houlden H, Blake J, Champion M, Flinter F, Robb SA, Page R, Rose M, Palace J, Crowe C, Longman C, Lunn MP, Rahman S, Reilly MM, Hanna MG. Pitceathly RD, et al. Neurology. 2012 Sep 11;79(11):1145-54. doi: 10.1212/WNL.0b013e3182698d8d. Epub 2012 Aug 29. Neurology. 2012. PMID: 22933740 Free PMC article.

9

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM Jr, Hodgson SV, Hunter A, Korf BR, Manchester D, Miesfeldt S, Murday VA, Nathanson KL, Parisi M, Pober B, Romano C, Eng C, et al. Marsh DJ, et al. Hum Mol Genet. 1999 Aug;8(8):1461-72. doi: 10.1093/hmg/8.8.1461. Hum Mol Genet. 1999. PMID: 10400993

10

Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Christ LA, Crowe CA, Micale MA, Conroy JM, Schwartz S. Christ LA, et al. Among authors: crowe ca. Am J Hum Genet. 1999 Nov;65(5):1387-95. doi: 10.1086/302606. Am J Hum Genet. 1999. PMID: 10521304 Free PMC article.

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