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Solid organ transplantation in primary mitochondrial disease: Proceed with caution.
Parikh, Sumit; Karaa, Amel; Goldstein, Amy; Ng, Yi S; Gorman, Grainne; Feigenbaum, Annette; Christodoulou, John; Haas, Richard; Tarnopolsky, Mark; Cohen, Bruce K; Dimmock, David; Feyma, Tim; Koenig, Mary K; Mundy, Helen; Niyazov, Dmitriy; Saneto, Russell P; Wainwright, Mark S; Wusthoff, Courtney; McFarland, Robert; Scaglia, Fernando.
  • Parikh S; Neurogenetics & Mitochondrial Disease, Center for Pediatric Neurology, Cleveland Clinic, Cleveland, OH, United States. Electronic address: parikhs@ccf.org.
  • Karaa A; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, United States.
  • Goldstein A; Center for Pediatric Neurology, Children's Hospital of Pittsburgh, Pittsburgh, PA, United States.
  • Ng YS; Wellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, UK.
  • Gorman G; Wellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, UK.
  • Feigenbaum A; Department of Medical Genetics, Rady Children's Hospital, San Diego, CA, United States.
  • Christodoulou J; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney and Disciplines of Paediatrics and Child Health and Genetic Medicine, University of Sydney, Sydney, Australia.
  • Haas R; Department of Pediatric Neurology, Rady Children's Hospital, San Diego, CA, United States.
  • Tarnopolsky M; Department of Pediatrics, Division of Neuromuscular and Neurometabolic Disease, McMaster University, Hamilton, ON, Canada.
  • Cohen BK; Department of Pediatric Neurology, Akron Children's Hospital, Akron, OH, United States.
  • Dimmock D; Department of Medical Genetics, Medical College of Wisconsin, Milwaukee, WI, United States.
  • Feyma T; Department of Pediatric Neurology, Gillette Children's Specialty Healthcare, St. Paul, MN, United States.
  • Koenig MK; Department of Pediatrics, Division of Child & Adolescent Neurology, The University of Texas Medical School at Houston, Houston, TX, United States.
  • Mundy H; Pediatric Metabolism, Evelina London Children's Healthcare, London, UK.
  • Niyazov D; Division of Medical Genetics, Department of Pediatrics, Ochsner Clinic Foundation, New Orleans, LA, United States.
  • Saneto RP; Department of Pediatric Neurology, Seattle Children's Hospital, Seattle, WA, United States.
  • Wainwright MS; Department of Pediatrics, Division of Neurology, Lurie Children's Hospital, Chicago, IL, United States.
  • Wusthoff C; Department of Pediatric Neurology, Lucile Packard Children's Hospital, Palo Alto, CA, United States.
  • McFarland R; Wellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, UK.
  • Scaglia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Baylor, TX, United States.
Mol Genet Metab ; 118(3): 178-184, 2016 07.
Article en En | MEDLINE | ID: mdl-27312126
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Rechazo de Injerto / Cardiopatías / Enfermedades Renales / Hepatopatías Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Año: 2016 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales / Rechazo de Injerto / Cardiopatías / Enfermedades Renales / Hepatopatías Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Año: 2016 Tipo del documento: Article