Richard H Haas

Summary

Affiliation: University of California
Country: USA

Publications

  1. ncbi request reprint Mitochondrial disease: a practical approach for primary care physicians
    Richard H Haas
    Department of Neurosciences, University of California San Diego, 9500 Gilman Dr, La Jolla, CA 92093 0935, USA
    Pediatrics 120:1326-33. 2007
  2. doi request reprint Autism and mitochondrial disease
    Richard H Haas
    Department of Neurosciences, UCSD Mitochondrial and Metabolic Disease Center, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA
    Dev Disabil Res Rev 16:144-53. 2010
  3. ncbi request reprint The evidence basis for coenzyme Q therapy in oxidative phosphorylation disease
    Richard H Haas
    Department of Neurosciences, UCSD Mitochondrial and Metabolic Disease Center, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093 0935, USA
    Mitochondrion 7:S136-45. 2007
  4. pmc The in-depth evaluation of suspected mitochondrial disease
    Richard H Haas
    Department of Neurosciences, University of California San Diego, La Jolla, CA and Rady Children s Hospital San Diego, San Diego, CA, United States
    Mol Genet Metab 94:16-37. 2008
  5. ncbi request reprint Chronic treatment of mitochondrial disease patients with dichloroacetate
    Bruce A Barshop
    Department of Pediatrics, University of California San Diego, La Jolla, CA 92093 0830, USA
    Mol Genet Metab 83:138-49. 2004
  6. pmc Pitfalls in the denaturing high-performance liquid chromatography analysis of mitochondrial DNA mutation
    Kok Seong Lim
    Department of Neurosciences, School of Medicine, University of California San Diego, La Jolla, California, USA
    J Mol Diagn 10:102-8. 2008
  7. pmc Impact of nucleoside reverse transcriptase inhibitors on mitochondrial DNA and RNA in human skeletal muscle cells
    Akihiko Saitoh
    Division of Infectious Diseases, Department of Pediatrics, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093 0672, USA
    Antimicrob Agents Chemother 52:2825-30. 2008
  8. ncbi request reprint The role of methionine in ethylmalonic encephalopathy with petechiae
    Karen A McGowan
    Institute of Molecular Genetics and the Department of Pediatrics, University of California San Diego, La Jolla 92093, USA
    Arch Neurol 61:570-4. 2004
  9. doi request reprint Assessing Bioenergetic Compromise in Autism Spectrum Disorder With 31P Magnetic Resonance Spectroscopy: Preliminary Report
    Beatrice A Golomb
    1Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, CA, USA
    J Child Neurol 29:187-93. 2014
  10. ncbi request reprint Quantitative mitochondrial DNA mutation analysis by denaturing HPLC
    Kok Seong Lim
    Department of Neurosciences, School of Medicine, University of California San Diego, La Jolla, CA 92093 0935, USA
    Clin Chem 53:1046-52. 2007

Collaborators

Detail Information

Publications12

  1. ncbi request reprint Mitochondrial disease: a practical approach for primary care physicians
    Richard H Haas
    Department of Neurosciences, University of California San Diego, 9500 Gilman Dr, La Jolla, CA 92093 0935, USA
    Pediatrics 120:1326-33. 2007
    ....
  2. doi request reprint Autism and mitochondrial disease
    Richard H Haas
    Department of Neurosciences, UCSD Mitochondrial and Metabolic Disease Center, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA
    Dev Disabil Res Rev 16:144-53. 2010
    ..Some patients with ASD phenotypes clearly have genetic-based primary mitochondrial disease. This review will examine the data linking autism and mitochondria...
  3. ncbi request reprint The evidence basis for coenzyme Q therapy in oxidative phosphorylation disease
    Richard H Haas
    Department of Neurosciences, UCSD Mitochondrial and Metabolic Disease Center, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093 0935, USA
    Mitochondrion 7:S136-45. 2007
    ..This paper discusses the current state of the evidence supporting the use of CoQ10 in mitochondrial disease...
  4. pmc The in-depth evaluation of suspected mitochondrial disease
    Richard H Haas
    Department of Neurosciences, University of California San Diego, La Jolla, CA and Rady Children s Hospital San Diego, San Diego, CA, United States
    Mol Genet Metab 94:16-37. 2008
    ..The aim of this work is to facilitate the diagnosis of mitochondrial disease by geneticists, neurologists, and other metabolic specialists who face the challenge of evaluating patients of all ages with suspected mitochondrial disease...
  5. ncbi request reprint Chronic treatment of mitochondrial disease patients with dichloroacetate
    Bruce A Barshop
    Department of Pediatrics, University of California San Diego, La Jolla, CA 92093 0830, USA
    Mol Genet Metab 83:138-49. 2004
    ....
  6. pmc Pitfalls in the denaturing high-performance liquid chromatography analysis of mitochondrial DNA mutation
    Kok Seong Lim
    Department of Neurosciences, School of Medicine, University of California San Diego, La Jolla, California, USA
    J Mol Diagn 10:102-8. 2008
    ....
  7. pmc Impact of nucleoside reverse transcriptase inhibitors on mitochondrial DNA and RNA in human skeletal muscle cells
    Akihiko Saitoh
    Division of Infectious Diseases, Department of Pediatrics, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093 0672, USA
    Antimicrob Agents Chemother 52:2825-30. 2008
    ..These findings may be of particular importance in developing countries, where ddI is widely used for first-line treatment of HIV-infected children...
  8. ncbi request reprint The role of methionine in ethylmalonic encephalopathy with petechiae
    Karen A McGowan
    Institute of Molecular Genetics and the Department of Pediatrics, University of California San Diego, La Jolla 92093, USA
    Arch Neurol 61:570-4. 2004
    ..The nature of the molecular defect in this subgroup is unknown, and the source of the ethylmalonic acid has been unclear...
  9. doi request reprint Assessing Bioenergetic Compromise in Autism Spectrum Disorder With 31P Magnetic Resonance Spectroscopy: Preliminary Report
    Beatrice A Golomb
    1Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, CA, USA
    J Child Neurol 29:187-93. 2014
    ....
  10. ncbi request reprint Quantitative mitochondrial DNA mutation analysis by denaturing HPLC
    Kok Seong Lim
    Department of Neurosciences, School of Medicine, University of California San Diego, La Jolla, CA 92093 0935, USA
    Clin Chem 53:1046-52. 2007
    ..The quantification and mathematical modeling of DHPLC results is, however, underexplored...
  11. ncbi request reprint Pyruvate carboxylase deficiency--insights from liver transplantation
    William L Nyhan
    Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA
    Mol Genet Metab 77:143-9. 2002
    ..Concentrations of glutamine in cerebrospinal fluid were low and did not improve with liver transplantation...
  12. pmc Normal platelet mitochondrial complex I activity in Huntington's disease
    William J Powers
    Department of Neurology, Washington University School of Medicine, St Louis, MO 63110, USA
    Neurobiol Dis 27:99-101. 2007
    ..Reductions > 10% were excluded with 80% confidence. A systemic defect in complex I activity is not present in early HD when striatal neuronal degeneration is already present...