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Pearson syndrome

  • Initial Experience in the Treatment of Inherited Mitochondrial Disease with EPI-743

    Initial Experience in the Treatment of Inherited Mitochondrial Disease with EPI-743

  • My Beloved Neutrophil Dr Boxer 2014 Neutropenia Family Conference

    My Beloved Neutrophil Dr Boxer 2014 Neutropenia Family Conference

  • Genes in Eyecare Geneseyedoc 3 W.M

    Genes in Eyecare Geneseyedoc 3 W.M

  • Haematological Abnormalities in Mitochondrial Disorders

    Haematological Abnormalities in Mitochondrial Disorders

  • Diagnosis of Mitochondrial Diseases: Clinical and Histological Study of Sixty Patients with Ragged Red Fibers

    Diagnosis of Mitochondrial Diseases: Clinical and Histological Study of Sixty Patients with Ragged Red Fibers

  • Mitochondrial Disease and Endocrine Dysfunction

    Mitochondrial Disease and Endocrine Dysfunction

  • 030626 Mitochondrial Respiratory-Chain Diseases

    030626 Mitochondrial Respiratory-Chain Diseases

  • Mitochondrial Diseases in North America an Analysis of the NAMDC Registry

    Mitochondrial Diseases in North America an Analysis of the NAMDC Registry

  • Diagnostic Approach in Infants and Children with Mitochondrial Diseases Ching-Shiang Chi*

    Diagnostic Approach in Infants and Children with Mitochondrial Diseases Ching-Shiang Chi*

  • View of Cryostat Section; Islet of Stained Cells Sur- Liver:Figure Ultrastructure 8 and Reaction for Cytochrome Oxidase Rounded by Unstained Parenchyma

    View of Cryostat Section; Islet of Stained Cells Sur- Liver:Figure Ultrastructure 8 and Reaction for Cytochrome Oxidase Rounded by Unstained Parenchyma

  • The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions

    The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions

  • EFNS Guidelines on the Molecular Diagnosis of Mitochondrial Disorders

    EFNS Guidelines on the Molecular Diagnosis of Mitochondrial Disorders

  • Congenital Neutropenia and Primary Immunodeficiency Diseases

    Congenital Neutropenia and Primary Immunodeficiency Diseases

  • Diagnosis, Management, and Follow-Up of Mitochondrial Disorders in Childhood: a Personalized Medicine in the New Era of Genome Sequence

    Diagnosis, Management, and Follow-Up of Mitochondrial Disorders in Childhood: a Personalized Medicine in the New Era of Genome Sequence

  • Disease Mechanisms in Mitochondrial Maintenance Disorders

    Disease Mechanisms in Mitochondrial Maintenance Disorders

  • Molecular Bases of Hearing Loss in Multi-Systemic Mitochondrial

    Molecular Bases of Hearing Loss in Multi-Systemic Mitochondrial

  • Mitochondrial DNA (Mtdna) Test Requisition

    Mitochondrial DNA (Mtdna) Test Requisition

  • 17-Month-Old Child with Pearson Syndrome and Corneal Haze – Case Report

    17-Month-Old Child with Pearson Syndrome and Corneal Haze – Case Report

Top View
  • Disease 217P
  • Mitochondrial DNA Deletion Syndromes
  • Pearson's Marrow-Pancreas Syndrome. a Multisystem Mitochondrial Disorder in Infancy
  • Why Is My Patient Neutropenic? 255
  • Mitochondrial Syndromes Revisited
  • Pearson Marrow-Pancreas Syndrome
  • Mitochondrial Disorders
  • Pearson Syndrome
  • Pearson Syndrome Associated with Hemophagocytic Syndrome in a Child
  • Mitochondrial Disorders a Review of Anesthetic Considerations.Pdf
  • Mtdna Deletion in an Iranian Infant with Pearson Marrow Syndrome
  • Introduction to Mitochondrial Disorders and Mito Resources by Susan Agrawal, Editor
  • Leigh Syndrome: One Disorder, More Than 75 Monogenic Causes
  • A61p27/00 (2006.01) A61p21/00 (2006.01)
  • Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
  • Mitochondrial Disease Heterogeneity: a Prognostic Challenge
  • (ISSN:2572-8776) Advances in Diagnosis of Mitochondrial Diseases
  • Parkinson's Disease


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