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Journal of Orofacial Orthopedics = Fortschritte Der Kieferorthopadie : Organ/Official Journal Deutsche Gesellschaft Fur Kieferorthopadie|July 10, 2026
Treatment effects of the Sander II appliance in class II therapy : A cephalometric, retrospective case-control studyCorinna L Seidel, Christof Haas, Richard Haas, et al.
Annals of Clinical and Translational Neurology|November 29, 2020
Triacetyluridine treats epileptic encephalopathy from CAD mutations: a case report and reviewAliya Frederick, Kimberly Sherer, Linda Nguyen, et al.
Pediatric Research|November 2, 2023
Seizures after initiation of rewarming in cooled infants with hypoxic ischaemic encephalopathyMalcolm R Battin, Suzanne L Davis, Marisa Gardner, et al.
Current Treatment Options in Neurology|November 7, 2009
A modern approach to the treatment of mitochondrial diseaseSumit Parikh, Russell Saneto, Marni J Falk, et al.
Therapeutic Advances in Chronic Disease|July 30, 2025
The profound implications of mitochondrial myopathy on activities of daily living: an observational qualitative study of standardized structured and semi-structured patient interviewsElizabeth M McCormick, James T Peterson, Joaquim Diego D Santos, et al.
Plos One|March 20, 2026
Effectiveness of a pharmacist diabetes coaching program: A propensity-matched retrospective analysisDaniel Amante, Samir Malkani, Richard Haas, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 29, 2012
Heteroplasmic mutations of the mitochondrial genome cause paradoxical effects on mitochondrial functionsChengkang Zhang, Vincent H Huang, Mariella Simon, et al.
Scientific Reports|February 24, 2022
Mitochondrial dysfunction associated with TANGO2 deficiencyPaige Heiman, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
Brain Communications|June 19, 2026
Efficacy and safety of pyrimidine nucleos(t)ide therapy in thymidine kinase 2 deficiencyMichio Hirano, Caterina Garone, Richard Haas, et al.
Neuromuscular Disorders : NMD|October 27, 2019
Fatigue in primary genetic mitochondrial disease: No rest for the wearySumit Parikh, Rachel Galioto, Brittany Lapin, et al.
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