DavidMBlakeMD

PubMed

• 79 citations
  X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1
  Catarina M. Quinzii, Tuan Vu, K. Christopher Min, Kurenai Tanji, Sandra Barral, Raji P. Grewal, Andrea Kattah, Pilir Camaño, David Otaegui, Teruhito Kunimatsu, David M...> ;American Journal of Human Genetics. 2008 Jan 10
• FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts.
  Topaloglu H, Brockington M, Yuva Y, Talim B, Haliloglu G, Blake D, Torelli S, Brown SC, Muntoni F> ;Neurology. 2003-03-25
• 296 citations
  Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
  Michio Hirano, Gabriella Silvestri, D. M. Blake, Anne Lombès, Carlo Minetti, Eduardo Bonilla, Arthur P. Hays, Robert E. Lovelace, Ian J. Butler, Tulio E. Bertorini, A....> ;Neurology. 1994 Apr 1
• 31 citations
  Persistent and transient “conduction block” in motor neuron diseases
  Dale J. Lange, Werner Trojaborg, T. D. McDonald, D. M. Blake> ;Muscle & Nerve. 1993 Sep 1
• 15 citations
  Adult Reye's syndrome A review with new evidence for a generalized defect in intramitochondrial enzyme processing
  R. Van Coster, Darryl C. De Vivo, D. M. Blake, Anne Lombès, R. Barrett, Salvatore DiMauro> ;Neurology. 1991 Nov 1
• 53 citations
  Clinical syndromes associated with ragged red fibers.
  Lewis P. Rowland, D. M. Blake, Michio Hirano, S Di Mauro, E. A. Schon, Arthur P. Hays, Darryl C. DeVivo> ;Revue Neurologique. 1991 Jan 1
• 212 citations
  Cerebrovascular complications of the use of the "crack" form of alkaloidal cocaine.
  Steven R. Levine, John C.M. Brust, N. Futrell, K. L. Ho, David Blake, C. Millikan, Lawrence M. Brass, Pierre B. Fayad, Lonni Schultz, James F. Selwa, K.M.A. Welch> ;The New England Journal of Medicine. 1990 Sep 13
• 104 citations
  Multifocal motor neuropathy with conduction block: Is it a distinct clinical entity?
  Dale J. Lange, Werner Trojaborg, Norman Latov, Arthur P. Hays, David S. Younger, Antonino Uncini, D. M. Blake, Michio Hirano, S. M. Burns, Robert E. Lovelace, Lewis P....> ;Neurology. 1992 Mar 1
• Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.
  Wilhelmsen, K. C., Blake, D. M., Lynch, T., Mabutas, J., De Vera, M., Neystat, M., Bernstein, M., Hirano, M., Gilliam, T. C., Murphy, P. L., Sola, M. D., Bonilla, E., ...> ;Ann Neurol. 1996 Apr
• Join now to see all