Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Metabolic myopathies].

J Lössner, H J Kühn

    Psychiatrie, Neurologie, Und Medizinische Psychologie
    |September 1, 1984
    PubMed
    Summary
    This summary is machine-generated.

    Metabolic myopathies are rare muscle disorders causing progressive weakness, pain, and stiffness. This review details specific conditions, their biochemical defects, and diagnostic methods.

    Related Experiment Videos

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    The apparent rates of crossbridge attachment and detachment estimated from ATPase activity in insect flight muscle.

    Biophysical journal·2009
    Same author

    [Correlation of clinical aspects as well as genotype and phenotype in Wilson's disease on the basis of epidemiologic, clinical and cranial MRI findings].

    Fortschritte der Neurologie-Psychiatrie·2006
    Same author

    Vacuum-ultraviolet beam array generation by flat micro-optical structures.

    Optics letters·2004
    Same author

    Expression patterns of erythropoietin and its receptor in the developing midbrain.

    Anatomy and embryology·2004
    Same author

    Investigation of fine-motor disturbances in Wilson's disease.

    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology·2003
    Same author

    Differential alteration of the nigrostriatal dopaminergic system in Wilson's disease investigated with [123I]ss-CIT and high-resolution SPET.

    European journal of nuclear medicine·2001
    Same journal

    [Comments on psychosomatic manifestations in ophthalmology].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    Same journal

    [Symptomatic myasthenia as a paraneoplastic syndrome in mixed-cell myelosis?].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    Same journal

    [Action and reaction elements as performance-modifying components of computer use in clinical psychology].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    Same journal

    [Clinical multiplicity of cerebrovascular disorders in childhood].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    Same journal

    [Endogenous psychoses in relation to absent phenylalanine hydroxylase activity in thrombocytes].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    Same journal

    [Pathology of inflammatory diseases of the central nervous system--an autopsy analysis 1967-1988].

    Psychiatrie, Neurologie, und medizinische Psychologie·1990
    See all related articles

    Area of Science:

    • Biochemistry
    • Neurology
    • Genetics

    Context:

    • Metabolic myopathies represent a rare but significant category of neuromuscular disorders.
    • These conditions manifest with diverse clinical presentations, including proximal, distal, or generalized muscle involvement.

    Purpose:

    • To describe key metabolic myopathies and their underlying biochemical defects.
    • To highlight essential biochemical investigative methods for diagnosis.

    Summary:

    • The abstract discusses the varying severity and presentation of metabolic myopathies, which can be progressive or episodic.
    • It outlines specific disorders, their associated biochemical anomalies, and emphasizes diagnostic approaches.

    Impact:

    • Provides a concise overview of metabolic myopathies for clinicians and researchers.
  • Aids in understanding the biochemical basis and diagnostic strategies for these rare disorders.