Ana Potic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy.
Journal: Molecular genetics and metabolism
Published: March 19, 2024
Hypomyelination caused by a novel homozygous pathogenic variant in FOLR1: complete clinical and radiological recovery with oral folinic acid therapy and review of the literature.
Journal: Orphanet journal of rare diseases
Published: January 19, 2023
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.
Journal: The Journal of clinical endocrinology and metabolism
Published: May 29, 2020
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.
Journal: Neurology
Published: December 23, 2019
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene.
Journal: Molecular genetics and metabolism reports
Published: October 19, 2016
CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation.
Journal: Journal of the neurological sciences
Published: July 03, 2015
Neurogenic bladder and neuroendocrine abnormalities in Pol III-related leukodystrophy.
Journal: BMC neurology
Published: September 29, 2014
Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variant.
Journal: Journal of neurology
Published: March 20, 2013
4H syndrome with late-onset growth hormone deficiency caused by POLR3A mutations.
Journal: Archives of neurology
Published: March 28, 2012
Childhood cerebral X-linked adrenoleukodystrophy more than 5 years after hematopoietic cell transplantation: the first case from Serbia and southeastern Europe.
Journal: Journal of child neurology
Published: July 27, 2010
Showing 1-10 of 10
Last Updated: 09/26/2026