Cognitive impairment in Duchenne muscular dystrophy

[1]  L. Kunkel,et al.  The structural and functional diversity of dystrophin , 1993, Nature Genetics.

[2]  Richard S. J. Frackowiak,et al.  The neural correlates of the verbal component of working memory , 1993, Nature.

[3]  M. Passos-Bueno,et al.  A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation , 1992, Neuromuscular Disorders.

[4]  N. Bresolin,et al.  Congenital myopathy associated with abnormal accumulation of desmin and dystrophin , 1992, Neuromuscular Disorders.

[5]  J. Signoret,et al.  Cognitive functions in duchenne muscular dystrophy: A reappraisal and comparison with spinal muscular atrophy , 1992, Neuromuscular Disorders.

[6]  A. Covone,et al.  Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR. , 1992, American journal of human genetics.

[7]  S. Petersen,et al.  Impaired non-motor learning and error detection associated with cerebellar damage. A single case study. , 1992, Brain : a journal of neurology.

[8]  G. V. Ommen,et al.  Mapping of dystrophin brain promoter: A deletion of this region is compatible with normal intellect , 1991, Neuromuscular Disorders.

[9]  J. Schmahmann.  An emerging concept. The cerebellar contribution to higher function. , 1991, Archives of neurology.

[10]  M. Passos-Bueno,et al.  Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy. , 1991, American journal of medical genetics.

[11]  Simon C Watkins,et al.  Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons , 1990, Nature.

[12]  P. Harper,et al.  Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA , 1990, Clinical genetics.

[13]  Margaret A. Johnson,et al.  Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy , 1989, Journal of the Neurological Sciences.

[14]  M. Bobrow,et al.  Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. , 1989, Journal of medical genetics.

[15]  Karl J. Friston,et al.  Localisation in PET Images: Direct Fitting of the Intercommissural (AC—PC) Line , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  M. W. Thompson,et al.  Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene. , 1989, American journal of human genetics.

[17]  M. Savontaus,et al.  Gene deletions in X-linked muscular dystrophy. , 1989, American journal of human genetics.

[18]  P. Einat,et al.  Duchenne muscular dystrophy gene product is not identical in muscle and brain , 1989, Nature.

[19]  R A Gibbs,et al.  Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. , 1988, Nucleic acids research.

[20]  J. Talairach,et al.  Co-Planar Stereotaxic Atlas of the Human Brain: 3-Dimensional Proportional System: An Approach to Cerebral Imaging , 1988 .

[21]  L. Kunkel,et al.  Cell and fiber type distribution of dystrophin , 1988, Neuron.

[22]  Jamel Chelly,et al.  Transcription of the dystrophin gene in human muscle and non-muscle tissues , 1988, Nature.

[23]  A. Hurley,et al.  LANGUAGE AND LEARNING DISORDERS OF OLDER BOYS WITH DUCHENNE MUSCULAR DYSTROPHY , 1988, Developmental medicine and child neurology.

[24]  Eric P. Hoffman,et al.  Dystrophin: The protein product of the duchenne muscular dystrophy locus , 1987, Cell.

[25]  M. Koenig,et al.  Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals , 1987, Cell.

[26]  C. D. Arnett,et al.  Glucose Metabolic Rate Kinetic Model Parameter Determination in Humans: The Lumped Constants and Rate Constants for [18F]Fluorodeoxyglucose and [11C]Deoxyglucose , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[27]  J. Aldridge,et al.  A strategy to reveal high-frequency RFLPs along the human X chromosome. , 1984, American journal of human genetics.

[28]  J. Miller,et al.  Clinical investigation in duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history , 1983, Muscle & nerve.

[29]  L. Binder.  Constructional strategies on complex figure drawings after unilateral brain damage. , 1982, Journal of clinical neuropsychology.

[30]  B. Milner,et al.  Performance of complex arm and facial movements after focal brain lesions , 1981, Neuropsychologia.

[31]  V. Dubowitz,et al.  Intellect and Behaviour in Duchenne Muscular Dystrophy , 1981, Developmental medicine and child neurology.

[32]  M. Brooke,et al.  Clinical trial in duchenne dystrophy. I. The design of the protocol , 1981, Muscle & nerve.

[33]  N. Karagan,et al.  Intellectual functioning in non‐Duchenne muscular dystrophy , 1981, Neurology.

[34]  T. Okuno,et al.  Central nervous system involvement in progressive muscular dystrophy. , 1980, Archives of disease in childhood.

[35]  E. Renzi,et al.  Normative Data and Screening Power of a Shortened Version of the Token Test , 1978, Cortex.

[36]  M. Reivich,et al.  THE [14C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1 , 1977, Journal of neurochemistry.

[37]  A. Emery,et al.  Clinical studies in benign (Becker type) X‐linked muscular dystrophy , 1976, Clinical genetics.

[38]  T. Munsat,et al.  Evidence for early impairment of verbal intelligence in Duchenne muscular dystrophy , 1974, Archives of disease in childhood.

[39]  V. Dubowitz,et al.  The central nervous system in Duchenne muscular dystrophy. , 1969, Brain : a journal of neurology.

[40]  V. McKusick.  Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes , 1983 .

[41]  J. Orbach.  Frontal Granular Cortex and Behavior. , 1964 .

[42]  E. Renzi,et al.  The token test: A sensitive test to detect receptive disturbances in aphasics. , 1962, Brain : a journal of neurology.

[43]  P. Vignos,et al.  Intellectual function in childhood progressive muscular dystrophy. , 1962, Pediatrics.

[44]  J. Hutchinson.  NOTES ON THE SYMPTOM-SIGNIFICANCE OF DIFFERENT STATES OF THE PUPIL. , 1878 .

[45]  Philip M. Corsi.  Human memory and the medial temporal region of the brain. , 1972 .

[46]  L B Taylor,et al.  Localisation of cerebral lesions by psychological testing. , 1969, Clinical neurosurgery.