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European Journal of Human Genetics : EJHG|June 17, 2004
Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cellsMartina T McDonnell, Andrew M Schaefer, Emma L Blakely, et al.
Harvard Review of Psychiatry|April 17, 2008
Cognitive-behavioral intervention with young anxious childrenDina R Hirshfeld-Becker, Bruce Masek, Aude Henin, et al.
The New England Journal of Medicine|February 24, 2000
Orthostatic intolerance and tachycardia associated with norepinephrine-transporter deficiencyJ R Shannon, N L Flattem, J Jordan, et al.
Molecular and Cellular Neurosciences|March 29, 2001
Autocrine regulation of norepinephrine transporter expressionZ G Ren, P Pörzgen, J M Zhang, et al.
Cancer Causes & Control : CCC|May 2, 2020
Differences in cancer survival by remoteness of residence: an analysis of data from a population-based cancer registryNina Afshar, Dallas R English, James A Chamberlain, et al.
Development (Cambridge, England)|February 4, 2005
Developmental stage determines the effects of MYC in the mammary epitheliumCollin M Blakely, Louis Sintasath, Celina M D'Cruz, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Human Mutation|September 2, 2011
A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutationsJohn W Yarham, Mazhor Al-Dosary, Emma L Blakely, et al.
Mitochondrion|December 14, 2011
A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunitsKate Craig, Matthew J Young, Emma L Blakely, et al.
Gastroenterology Clinics of North America|November 1, 2019
Preparing the Patient for Home Parenteral Nutrition and for a Successful Course of TherapyNancy Evans Stoner, Phyllis Schiavone, Bruce P Kinosian, et al.
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