Lena Samuelsson
Goeteborg, O 41119, Sweden
Last Updated: 09/26/2026
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Found 11 publications
A randomized controlled trial of a new intervention in early symptomatic syndromes eliciting neurodevelopmental clinical examinations: PR-ESSENCE.
Journal: European child & adolescent psychiatry
Published: December 06, 2020
Hyperestrogenism Affects Adult Height Outcome in Growth Hormone Treated Boys With Silver-Russell Syndrome.
Journal: Frontiers in endocrinology
Published: August 20, 2018
On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion.
Journal: American journal of medical genetics. Part A
Published: January 02, 2017
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy.
Journal: American journal of human genetics
Published: August 16, 2016
CTNND2-a candidate gene for reading problems and mild intellectual disability.
Journal: Journal of medical genetics
Published: December 05, 2014
Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability.
Journal: European journal of medical genetics
Published: June 01, 2014
UBE2A deficiency syndrome: a report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene.
Journal: American journal of medical genetics. Part A
Published: March 03, 2014
An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities.
Journal: Journal of human genetics
Published: January 26, 2014
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
Journal: Nature genetics
Published: May 07, 2012
Effects on airways of short-term exposure to two kinds of wood smoke in a chamber study of healthy humans.
Journal: Inhalation toxicology
Published: January 07, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026