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Publications by Kirsi J. Kiiski
Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Related publications
Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Rare Structural Myopathy: Nemaline Myopathy
Turk Pediatri Arsivi
Child Health
Pediatrics
Perinatology
Fatal Nemaline Myopathy in Infancy
Canadian Journal of Neurological Sciences
Medicine
Neurology
Cap Myopathy
Dominantly Inherited Drusen of Bruch's Membrane.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Nemaline Myopathy in an Adult With Primary Hypothyroidism
Canadian Journal of Neurological Sciences
Medicine
Neurology
Anaesthetic Implications of Nemaline Rod Myopathy
Canadian Journal of Anaesthesia
Medicine
Anesthesiology
Pain Medicine
Further Delineation of the Phenotype Caused by a Novel Large Homozygous Deletion of GRID2 Gene in an Adult Patient
Clinical Case Reports
Medicine
Abnormal Actin Binding of Aberrant Β-Tropomyosins Is a Molecular Cause of Muscle Weakness inTPM2-related Nemaline and Cap Myopathy
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology