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Molecular Genetics and Metabolism|March 21, 2006
Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant loadGregory M Enns, Ren-Kui Bai, Anita E Beck, et al.
Neurosurgical Focus|March 18, 2008
Cellular therapy for childhood neurodegenerative disease. Part I: rationale and preclinical studiesDaniel J Guillaume, Stephen L Huhn, Nathan R Selden, et al.
Neurosurgical Focus|March 18, 2008
Cellular therapy for childhood neurodegenerative disease. Part II: clinical trial design and implementationNathan R Selden, Daniel J Guillaume, Robert D Steiner, et al.
Molecular Genetics and Metabolism|August 5, 2019
Perspectives on urea cycle disorder management: Results of a clinician surveyGregory M Enns, Marty H Porter, Megan Francis-Sedlak, et al.
Obstetrics and Gynecology|May 3, 2005
Postpartum "psychosis" in mild argininosuccinate synthetase deficiencyGregory M Enns, William E O'Brien, Keiko Kobayashi, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Evidence of redox imbalance in a patient with succinic semialdehyde dehydrogenase deficiencyAnna-Kaisa Niemi, Candida Brown, Tereza Moore, et al.
Neurosurgery|September 8, 2005
Paradoxical cerebral herniation secondary to lumbar puncture after decompressive craniectomy for a large space-occupying hemispheric stroke: case reportAdetokunbo A Oyelese, Gary K Steinberg, Stephen L Huhn, et al.
Neurosurgery|July 11, 2007
Cerebral myiasis associated with angiosarcoma of the scalp: case reportSamuel H Cheshier, Simon R Bababeygy, Dominique Higgins, et al.
Mitochondrion|September 26, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and managementSumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.
Pediatric Neurology|March 25, 2008
Dopa-responsive dystonia presenting as delayed and awkward gaitBenjamin N R Cheyette, Sarah N R Cheyette, Kristina Cusmano-Ozog, et al.
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