Jewell C. Ward

Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene

Charles E. Schwartz, Melanie May, Nancy J. Carpenter et al. · The American Journal of Human Genetics · 2005 · 366 citations · Full text

Molecular Physiology, Mendelian Disorder, Genetic Disorder +5

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis

Saul W. Brusilow, Mark M. Danney, Lewis Waber et al. · New England Journal of Medicine · 1984 · 233 citations

<i>CRTAP</i>and<i>LEPRE1</i>mutations in recessive osteogenesis imperfecta

Dustin Baldridge, Ulrike Schwarze, Roy Morello et al. · Human Mutation · 2008 · 207 citations · Full text

Sclerostin, Genetics, Unfolded Collagen +18

Effect of beta-adrenergic blockade on aortic root rate of dilation in the Marfan syndrome

Mubadda A. Salim, Bruce S. Alpert, Jewell C. Ward et al. · The American Journal of Cardiology · 1994 · 144 citations

Marfan Syndrome, Cardiovascular Disease, Beta-adrenergic Blockade +5

Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: Report of five new cases and review

Enik K rm n Pivnick, Brad Angle, Robert A. Kaufman et al. · American Journal of Medical Genetics · 2000 · 81 citations