CraigLHyserMD

PubMed

• 32 citations
  Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.
  Barbara Weiffenbach, Rebecca G. Bagley, Kathleen M. Falls, Craig Hyser, D. Storvick, Stephen J. Jacobsen, Paul Schultz, Jerry R. Mendell, K Willems van Dijk, E. C. B. ...> ;American Journal of Human Genetics. 1992 Aug 1
• 106 citations
  Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.
  Mansoor Sarfarazi, Cisca Wijmenga, Meena Upadhyaya, Barbara Weiffenbach, Craig Hyser, Kathy Mathews, Jeffrey Murray, John W. Gilbert, Margaret A. Pericak-Vance, Peter ...> ;American Journal of Human Genetics. 1992 Jan 1
• 4 citations
  Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.
  Barbara Weiffenbach, Rebecca G. Bagley, Kathleen M. Falls, JoAnn Dubois, Craig Hyser, D. Storvick, Paul Schultz, Jerry R. Mendell, Eric C. B. Millner, Stephen J. Jacob...> ;Mammalian Genome. 1992 Jan 1
• Unraveling the mysteries of Duchenne and Becker muscular dystrophy.
  Craig Hyser> ;Molecular and Chemical Neuropathology. 1989 Feb 1
• 4 citations
  Scapuloperoneal neuropathy: A distinct clinicopathologic entity
  Craig L. Hyser, John T. Kissel, John R. Warmolts, Jerry R. Mendell> ;Journal of the Neurological Sciences. 1988 Oct 1
• 14 citations
  Recent advances in Duchenne and Becker muscular dystrophy.
  Craig Hyser, Jerry R. Mendell> ;Neurologic Clinics. 1988 Aug 1
• 9 citations
  Genetic heterogeneity in Duchenne dystrophy.
  Craig Hyser, Michael A. Province, Robert C. Griggs, Jerry R. Mendell, Gerald M. Fenichel, Michael H. Brooke, J. P. Miller, R. Polakowska, R. A. Doherty, S. Quirk> ;Annals of Neurology. 1987 Oct 1
• 6 citations
  Carrier assessment for mothers and sisters of isolated Duchenne dystrophy cases The importance of serum enzyme determinations
  Craig Hyser, R. A. Doherty, Robert C. Griggs, J. R. Mendell, R. Polakowska, S. Quirk, Michael H. Brooke, G. M. Fenichel> ;Neurology. 1987 Sep 1
• 21 citations
  Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy
  Craig Hyser, Robert C. Griggs, J. R. Mendell, R. Polakowska, S. Quirk, Michael H. Brooke, G. M. Fenichel, R. A. Doherty> ;Neurology. 1987 Jan 1
• 22 citations
  Status epilepticus after baclofen withdrawal.
  Craig L. Hyser, Miles E. Drake> ;Journal of the National Medical Association. 1984 May 1
• 15 citations
  Myoclonus Induced by Metoclopramide Therapy
  Craig L. Hyser, Miles E. Drake> ;Archives of Internal Medicine. 1983 Nov 1
• Three cases of amyotrophic lateral sclerosis in a common occupational environment.
  Hyser, C. L., Kissel, J. T., Mendell, J. R.> ;J Neurol. 1987 Aug
• Characterization of a murine model for human bismuth encephalopathy.
  Ross, J. F., Sahenk, Z., Hyser, C., Mendell, J. R., Alden, C. L.> ;Neurotoxicology. 1988
• Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
  Kunkel, L. M., Hejtmancik, J. F., Caskey, C. T., Speer, A., Monaco, A. P., Middlesworth, W., Colletti, C. A., Bertelson, C., Müller, U., Bresnan, M., Shapiro, F., Tant...> ;Nature. 1986 Jul 03
• Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy.
  Chutkow, J. G., Hyser, C. L., Edwards, J. A., Heffner, R. R., Czyrny, J. J.> ;Neurology. 1987 Jul
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