Related Experiment Videos
[DNA duplication in hereditary type Ia motor and sensory neuropathy (Charcot-Marie-Tooth disease)]
J E Hoogendijk1, F Baas, M de Visser
1Academisch Medisch Centrum, afd. Neurologie, Amsterdam.
Nederlands Tijdschrift Voor Geneeskunde
|December 21, 1991
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia.
European journal of neurology·2026
Awareness of bone strength in patients with neuromuscular disorders: ERN EURO-NMD clinician survey and European patient survey.
Journal of the neurological sciences·2025
Improved ROSC rates in out-of-hospital cardiac arrest patients after introduction of a text message alert system for trained volunteers.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation·2022
Distal muscle weakness and optic atrophy without central nervous system involvement in a patient with a homozygous missense mutation in the C19ORF12-gene.
Clinical neurology and neurosurgery·2021
[Multidisciplinary Management of Bone Metastases in Clinical Practice].
Nederlands tijdschrift voor geneeskunde·2026
[Consequences of celiac disease in an unaccompanied minor Eritrean refugee: severe intramedullary hemolytic anemia due to vitamin B12deficiency].
Nederlands tijdschrift voor geneeskunde·2026
[How residents develop virtues: A qualitative longitudinal study].
Nederlands tijdschrift voor geneeskunde·2026
[Fluctuating hormones, fluctuating mood? Depression in perimenopause].
Nederlands tijdschrift voor geneeskunde·2026
[Idiopathic normal pressure hydrocephalus: diagnosis or dilemma?]
Nederlands tijdschrift voor geneeskunde·2026
[Medical evacuations from conflict areas; practice and politics].
Nederlands tijdschrift voor geneeskunde·2026
The brain fatigue syndrome: a cross-diagnostic phenomenon.
Frontiers in human neuroscience·2026
Role of Miro1 in Mitochondrial Dysfunction and Neurodegeneration in Huntington's Disease.
Current neurovascular research·2026
Juvenile Huntington Disease With Cerebellar-Predominant Atrophy Identified by Genome Sequencing.
Annals of clinical and translational neurology·2026