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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.
Lancet Neurol. 2010 Jan;9(1):77-93. doi: 10.1016/S1474-4422(09)70271-6. Epub 2009 Nov 27.
Lancet Neurol. 2010.
PMID: 19945913
Review.
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders.
McConkie-Rosell A, Abrams L, Finucane B, Cronister A, Gane LW, Coffey SM, Sherman S, Nelson LM, Berry-Kravis E, Hessl D, Chiu S, Street N, Vatave A, Hagerman RJ.
McConkie-Rosell A, et al. Among authors: vatave a.
J Genet Couns. 2007 Oct;16(5):593-606. doi: 10.1007/s10897-007-9099-y. Epub 2007 May 12.
J Genet Couns. 2007.
PMID: 17497108
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Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005.
Kenneson A, Vatave A, Finkel R.
Kenneson A, et al. Among authors: vatave a.
Neurology. 2010 Sep 14;75(11):982-9. doi: 10.1212/WNL.0b013e3181f25e5b.
Neurology. 2010.
PMID: 20837966
Free PMC article.
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