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City Boston / Paris / / Company Shafiq SA. / Rimalovski AB / Matsushita / Neuropathologists Inc. / Henriksson KG. / GE / Meijer AE / Kim SA / Donnelly / McCormick / Knudsen / / Currency pence / / / Facility National Institute of Health / Children’s Hospital / Women’s Hospital / / IndustryTerm gas exchange / satellite cell nuclei / protein product / oil / reaction product / splice site / carrier mother / intermyofibrillar network / document carrier status / / MedicalCondition congenital myotonic dystrophy / myopia / severe myopathy / PeriCentronuclear myopathy / JE / X-linked disorder / Chronic neuropathies / rare familial neuromuscular disease / Familial neuromuscular disease / Payrastre B. Phosphoinositide signaling disorders / myopathy / Charcot-Marie-Tooth syndrome / external ophthalmoplegia / autosomal recessive centronuclear myopathy / X-linked myotubular myopathy / Familial centronuclear myopathy / Ferrari G. Centronuclear myopathy / muscle weakness / congenital myopathy / muscle diseases / miscarriages / slowly progressive myopathy / hepatic dysfunction / dominant centronuclear myopathy / ophthalmoplegia / slowly progressive muscle weakness / neuromuscular disease / neonatal centronuclear/ myotubular myopathy / myotubular myopathies / X-linked recessive myotubular myopathy / disorder / unrelated X-linked myotubular myopathy / infantile spinal muscular atrophy / e.g. myotonic dystrophy / X-linked recessive disorder / centronuclear myopathies / human diseases / nephrocalcinosis / severe disease / jaw malocclusion / scoliosis / myopathies / gallstones / dissociation / restrictive lung disease / early-onset glaucoma / mild myotubular myopathy / Centronuclear Myopathies Christopher R. Pierson / tumor / primary myopathies / paralysis / limb-girdle muscular dystrophies / necrosis / premature births / congenital myopathies / haploid DNA disease / ophthalmoparesis / contiguous gene syndrome / genetic disease / familial muscular disorder / disease / Centronuclear myopathy / Myofiber necrosis / Weber U. Familial centronuclear myopathy / DeSa D. Infantile centronuclear myopathy / myotonic dystrophy / autosomal disorders / adult onset myotubular myopathy / adult centronuclear myopathies / pyloric stenosis / Charcot-Marie-Tooth disease / type 4B Charcot-Marie-Tooth disease / tumour / myotubular myopathy / polyhydramnios / facial muscle weakness / diseases / severe myopathies / muscular dystrophies / segmented demyelination / respiratory insufficiency / hypotonia / terms myotubular myopathy / congenital muscular dystrophy / generalized progressive myopathy / deficiency / pathologically defined disorders / contractures / Mielke U. Centronuclear myopathy / inflammation / endomysial fibrosis / Neonatal myotubular myopathy / profound global hypotonia / human disease / syndrome / Fibrosis / disorders / autosomal centronuclear myopathy / / MedicalTreatment tube feeding / counseling / mechanical ventilation / / Organization Harvard Medical School / Division of Genetics / Joshua Frase Foundation / National Institute of Health / Department of Pathology / Women’s Hospital / Children’s Hospital Boston / American Association of Neuropathologists / European NeuroMuscular Center / Association of SET / Genomic / Division of Neuropathology / / Person Arch Neurol / Peter Kang / Howard Mulhern / Ann Neurol / Alan H. Beggs / Pankaj Agrawal / Bryce Due / Acta Neuropathol / Jung J. Morphologic / Kinga Tomczak / Key Words / Behzad Moghadaszadeh / Anthony A. Amato / Michael Greenberg / Van Wijngaarden / Christopher R. Pierson / Umberto De Girolami / / Position second messenger / additional candidate / Carpenter / Sarnat HB / author / Singer / important mediator / / Product vitamin K / / ProvinceOrState Saskatchewan / DNA / Massachusetts / / RadioStation Tome FM / Stadhouders AM / / Technology alpha / Genomics / cell signaling / apoptosis / genotype / / URL www.genetests / / SocialTag 
J Neuropathol Exp Neurol Copyright Ó 2005 by the American Association of Neuropathologists, Inc. Vol. 64, No. 7 July 2005 pp. 555–564