Works matching IS 00778923 AND DT 1999 AND VI 883 AND IP 1
Results: 73
Prenatal Diagnosis of Charcot-Marie-Tooth Disease Type 1A.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 457, doi. 10.1111/j.1749-6632.1999.tb08609.x
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Mutation Testing in Charcot-Marie-Tooth Neuropathy.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 383, doi. 10.1111/j.1749-6632.1999.tb08599.x
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Phenotypic Manifestations in French-Canadian Population with Charcot-Marie-Tooth Disease Type 1A Associated with 17p11.2 Duplication.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 497, doi. 10.1111/j.1749-6632.1999.tb08620.x
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Distal Hereditary Motor Neuronopathy of the Jerash Type.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 439, doi. 10.1111/j.1749-6632.1999.tb08604.x
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Human Nerve Pathology Caused by Different Mutational Mechanisms of the PMP22 Gene.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 336, doi. 10.1111/j.1749-6632.1999.tb08595.x
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Trembler as a Mouse Model of CMT1A?
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 262, doi. 10.1111/j.1749-6632.1999.tb08588.x
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Historical Perspective of Defining Charcot-Marie-Tooth Type 1B.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 6, doi. 10.1111/j.1749-6632.1999.tb08561.x
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Introduction to the Third International Symposium on Charcot-Marie-Tooth Disorders.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. xiii, doi. 10.1111/j.1749-6632.1999.tb08559.x
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P<sub>0</sub>-Deficient Knockout Mice as Tools to Understand Pathomechanisms in Charcot-Marie-Tooth 1B and P<sub>0</sub>-Related Déjérine-Sottas Syndrome.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 273, doi. 10.1111/j.1749-6632.1999.tb08589.x
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The Biology of Chronically Denervated Schwann Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 215, doi. 10.1111/j.1749-6632.1999.tb08584.x
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New Vistas on the Pathomechanism of Charcot-Marie-Tooth and Related Peripheral Neuropathies.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 152, doi. 10.1111/j.1749-6632.1999.tb08578.x
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P<sub>0</sub>- Cre Transgenic Mice for Inactivation of Adhesion Molecules in Schwann Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 116, doi. 10.1111/j.1749-6632.1999.tb08574.x
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Schwann Cell-Derived Desert Hedgehog Signals Nerve Sheath Formation.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 196, doi. 10.1111/j.1749-6632.1999.tb08582.x
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Why Do Schwann Cells Survive in the Absence of Axons?
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 109, doi. 10.1111/j.1749-6632.1999.tb08573.x
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Regulation of Myelin-Specific Gene Expression: Relevance to CMT1.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 91, doi. 10.1111/j.1749-6632.1999.tb08572.x
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Molecular Mechanisms for CMT1A Duplication and HNPP Deletion.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 22, doi. 10.1111/j.1749-6632.1999.tb08563.x
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Schwann Cell-Axon Interactions in Charcot-Marie-Tooth Disease.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 77, doi. 10.1111/j.1749-6632.1999.tb08571.x
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HMSN and HNPP: Laboratory Service Provision in the South West of England-Two Years' Experience.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 500, doi. 10.1111/j.1749-6632.1999.tb08621.x
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Characteristics of Gap Junction Channels in Schwann Cells from Wild-Type and Connexin-Null Mice.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 533, doi. 10.1111/j.1749-6632.1999.tb08630.x
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Electrodiagnostic Findings in CMTX: A Disorder of the Schwann Cell and Peripheral Nerve Myelin.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 504, doi. 10.1111/j.1749-6632.1999.tb08622.x
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A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 481, doi. 10.1111/j.1749-6632.1999.tb08616.x
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Altered Assembly of Gap Junction Channels Caused by COOH-Terminal Connexin32 Mutants of CMTX.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 526, doi. 10.1111/j.1749-6632.1999.tb08628.x
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Construction of a PAC Contig within the Distal Hereditary Motor Neuropathy Type II Candidate Region at 12q24.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 463, doi. 10.1111/j.1749-6632.1999.tb08611.x
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Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement: Clinical, Pathological, and Genetic Features.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 449, doi. 10.1111/j.1749-6632.1999.tb08607.x
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Alterations in Nodes of Ranvier and Schmidt-Lanterman Incisures in Charcot-Marie-Tooth Neuropathies.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 508, doi. 10.1111/j.1749-6632.1999.tb08623.x
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Overview of Charcot-Marie-Tooth Disease Type 1A.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 1, doi. 10.1111/j.1749-6632.1999.tb08560.x
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Charcot-Marie-Tooth 1A: Heterozygous T118M Mutation over a CMT1A Duplication Has No Influence on the Phenotype.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 485, doi. 10.1111/j.1749-6632.1999.tb08617.x
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Characterization of Targeted Connexin32-Deficient Mice: A Model for the Human Charcot-Marie-Tooth (X-Type) Inherited Disease.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 302, doi. 10.1111/j.1749-6632.1999.tb08592.x
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Trophic Factors in Neuron-Schwann Cell Interactions.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 427, doi. 10.1111/j.1749-6632.1999.tb08603.x
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A Second Family with Autosomal Dominant Burning Feet Syndrome.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 445, doi. 10.1111/j.1749-6632.1999.tb08606.x
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Neurofibromin, the Neurofibromatosis Type 1 Ras-GAP, Is Required for Appropriate P<sub>0</sub> Expression and Myelination.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 203, doi. 10.1111/j.1749-6632.1999.tb08583.x
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Overcoming Cellular Immunity to Prolong Adenoviral-Mediated Gene Expression in Sciatic Nerve.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 397, doi. 10.1111/j.1749-6632.1999.tb08601.x
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The 'CMT Rat': Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 254, doi. 10.1111/j.1749-6632.1999.tb08587.x
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Peripheral Nerve Dysmyelination Due to P<sub>0</sub> Glycoprotein Overexpression Is Dose-Dependent.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 294, doi. 10.1111/j.1749-6632.1999.tb08591.x
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Transgenic Mouse Models of CMT1A and HNPP.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 247, doi. 10.1111/j.1749-6632.1999.tb08586.x
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Overview of Hereditary Neuropathy with Liability to Pressure Palsies.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 14, doi. 10.1111/j.1749-6632.1999.tb08562.x
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Distal Hereditary Motor Neuronopathy of the Jerash Type.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 65, doi. 10.1111/j.1749-6632.1999.tb08569.x
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X-linked Charcot-Marie-Tooth Disease and Connexin32.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 36, doi. 10.1111/j.1749-6632.1999.tb08564.x
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Autosomal Recessive Hereditary Motor and Sensory Neuropathy with Focally Folded Myelin Sheaths (CMT4B).
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 47, doi. 10.1111/j.1749-6632.1999.tb08566.x
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A Clinical Review of Charcot-Marie-Tooth.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 69, doi. 10.1111/j.1749-6632.1999.tb08570.x
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Schwann Cell Apoptosis during Cell-Mediated Demyelination.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 518, doi. 10.1111/j.1749-6632.1999.tb08625.x
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Abnormal Schwann Cell-Axon Interactions in CMT Neuropathies: The Effects of Mutant Schwann Cells on the Axonal Cytoskeleton and Regeneration-Associated Myelination.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 415, doi. 10.1111/j.1749-6632.1999.tb08602.x
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A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 466, doi. 10.1111/j.1749-6632.1999.tb08612.x
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Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth Disease.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 477, doi. 10.1111/j.1749-6632.1999.tb08615.x
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Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and Results.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 389, doi. 10.1111/j.1749-6632.1999.tb08600.x
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The Anatomy and Cell Biology of Peripheral Myelin Protein-22.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 143, doi. 10.1111/j.1749-6632.1999.tb08577.x
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Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 60, doi. 10.1111/j.1749-6632.1999.tb08568.x
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Charcot-Marie-Tooth Disease Type 2.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 42, doi. 10.1111/j.1749-6632.1999.tb08565.x
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Human Schwann Cell Proliferation and IL-6 Production following TNF-α Stimulation in Vitro.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 520, doi. 10.1111/j.1749-6632.1999.tb08626.x
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Induction of Myelin Gene Expression in Murine Schwann Cells in Primary Culture and in a Schwann Cell Line.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 513, doi. 10.1111/j.1749-6632.1999.tb08624.x
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