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Laminopathy

  • Emery-Dreifuss Muscular Dystrophy: the Most Recognizable Laminopathy

    Emery-Dreifuss Muscular Dystrophy: the Most Recognizable Laminopathy

  • Three New Cases of Dilated Cardiomyopathy Caused by Mutations in LMNA Gene

    Three New Cases of Dilated Cardiomyopathy Caused by Mutations in LMNA Gene

  • Genetic Mutations and Mechanisms in Dilated Cardiomyopathy

    Genetic Mutations and Mechanisms in Dilated Cardiomyopathy

  • Deciphering Nuclear Mechanobiology in Laminopathy

    Deciphering Nuclear Mechanobiology in Laminopathy

  • Genetic Determinants Underlying Rare Diseases Identified Using Next-Generation Sequencing Technologies

    Genetic Determinants Underlying Rare Diseases Identified Using Next-Generation Sequencing Technologies

  • Lamin A/C Cardiomyopathy: Implications for Treatment

    Lamin A/C Cardiomyopathy: Implications for Treatment

  • Hippocampal LMNA Gene Expression Is Increased in Late-Stage Alzheimer’S Disease

    Hippocampal LMNA Gene Expression Is Increased in Late-Stage Alzheimer’S Disease

  • Atrial Fibrillation (ATRIA) Study

    Atrial Fibrillation (ATRIA) Study

  • Irreversible Modifications of Chromatin and the Nuclear Lamina: a Review Inside the Nuclear Origin of Alzheimer's Disease

    Irreversible Modifications of Chromatin and the Nuclear Lamina: a Review Inside the Nuclear Origin of Alzheimer's Disease

  • Genetic Disorder

    Genetic Disorder

  • Orphanet Report Series Rare Diseases Collection

    Orphanet Report Series Rare Diseases Collection

  • Paradoxical Aortic Stiffening and Subsequent Cardiac Dysfunction in Hutchinson-Gilford Progeria Syndrome

    Paradoxical Aortic Stiffening and Subsequent Cardiac Dysfunction in Hutchinson-Gilford Progeria Syndrome

  • Genetic Cardiomyopathies: the Lesson Learned from Hipscs

    Genetic Cardiomyopathies: the Lesson Learned from Hipscs

  • The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies Review Article

    The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies Review Article

  • (12) Patent Application Publication (10) Pub. No.: US 2010/0210567 A1 Bevec (43) Pub

    (12) Patent Application Publication (10) Pub. No.: US 2010/0210567 A1 Bevec (43) Pub

  • LMNA-Related Disorders

    LMNA-Related Disorders

  • Limb-Girdle Muscular Dystrophy with Severe Heart Failure Overlapping with Lipodystrophy in a Patient with LMNA Mutation P.Ser334del

    Limb-Girdle Muscular Dystrophy with Severe Heart Failure Overlapping with Lipodystrophy in a Patient with LMNA Mutation P.Ser334del

  • Case Report of Malouf Syndrome Not Associated with LMNA Gene Mutation

    Case Report of Malouf Syndrome Not Associated with LMNA Gene Mutation

Top View
  • Understanding Lamin A/C and Its Roles in Disease
  • How Often Do Medical Management Guidelines Change for People with Germline Genetic Findings?
  • An Omics View of Emery–Dreifuss Muscular Dystrophy
  • Lamin A/C Mechanotransduction in Laminopathies
  • Unweaving the Role of Nuclear Lamins in Neural Circuit Integrity
  • Wo 2009/046875 A2
  • Laminopathy (LMNA)
  • Lamin A/C Mutations Associated with Familial and Sporadic Cases of Dilated Cardiomyopathy in Koreans
  • A Complex LINC Between Nuclear Envelope and Pathology
  • Consequences of Lmna Exon 4 Mutations in Myoblast Function
  • Diagnosis and Treatment of Limb-Girdle Muscular Dystrophy
  • Sudden Cardiac Death in Young Athletes: Literature Review Of
  • Review LAMINOPATHIES
  • Brugada Syndrome (Brs)
  • Cardiac Involvement in Emery-Dreifuss Muscular Dystrophy and Related Management Strategies
  • Clinical Disease Presentation and ECG Characteristics of LMNA Mutation Carriers
  • Cardiac Arrhythmias in Muscular Dystrophies Associated with Emerinopathy and Laminopathy: a Cohort Study
  • Cardiomyopathies: an Overview


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