Atle Melberg
Uppsala, C, Sweden
Last Updated: 09/26/2026
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Found 15 publications
Inherited Ataxia and Intrathecal Baclofen for the Treatment of Spasticity and Painful Spasms.
Journal: Stereotactic and functional neurosurgery
Published: October 10, 2018
Glucose metabolism in the brain in LMNB1-related autosomal dominant leukodystrophy.
Journal: Acta neurologica Scandinavica
Published: May 21, 2018
LMNB1-related autosomal-dominant leukodystrophy: Clinical and radiological course.
Journal: Annals of neurology
Published: November 03, 2014
Recurrence of Susac Syndrome following 23 Years of Remission.
Journal: Case reports in neurology
Published: July 03, 2014
Does intrathecal baclofen have a place in the treatment of painful spasms in friedreich ataxia?
Journal: Case reports in neurology
Published: December 19, 2013
Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain.
Journal: Brain : a journal of neurology
Published: November 16, 2013
Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression.
Journal: Human mutation
Published: February 01, 2013
¹H-MR spectroscopy of adult-onset autosomal dominant leukodystrophy with autonomic symptoms.
Journal: Neuroradiology
Published: October 19, 2012
Reply to Brodehl et al.
Journal: European journal of human genetics : EJHG
Published: October 04, 2012
Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin.
Journal: Brain : a journal of neurology
Published: May 12, 2012
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutation.
Journal: European journal of human genetics : EJHG
Published: March 08, 2012
Last Updated: 09/26/2026