Maninder S. Chawla
Oslo, 0450, Norway
Last Updated: 09/26/2026
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Found 9 publications
A Homozygous Deep Intronic SNX14 Variant Activates Pseudo-Exon Inclusion in a Patient with SCAR20.
Journal: Genes
Published: February 11, 2026
Vocal Cord Paresis and Neuropathic Pain in Infantile Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation: A Case Report.
Journal: Case reports in neurology
Published: May 19, 2025
Arachidonic and docosahexaenoic acid supplementation and brain maturation in preterm infants; a double blind RCT.
Journal: Clinical nutrition (Edinburgh, Scotland)
Published: August 25, 2023
A man in his twenties with weakness and numbness in his legs.
Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: January 19, 2023
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria.
Journal: Human molecular genetics
Published: June 19, 2022
Iron accumulation in the motor cortex in amyotrophic lateral sclerosis.
Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: March 23, 2021
A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
Journal: European journal of neurology
Published: September 09, 2015
Two cases of acute severe flaccid myelitis associated with enterovirus D68 infection in children, Norway, autumn 2014.
Journal: Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin
Published: March 20, 2015
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Last Updated: 09/26/2026