Brian N. Andersen
Arhus, Denmark
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Recommendations for the diagnosis and management of cln3 disease (batten disease) using the Delphi consensus methodology.
Journal: Orphanet journal of rare diseases
Published: April 22, 2025
Spring-assisted cranioplasty for children with craniosynostosis
Journal: Ugeskrift for laeger
Published: March 28, 2025
Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants.
Journal: European journal of medical genetics
Published: September 15, 2023
Autosomal recessive Noonan-like syndrome caused by homozygosity for a previously unreported variant in SPRED2.
Journal: European journal of medical genetics
Published: October 28, 2022
Incidence of Aicardi-Goutières syndrome and KCNT1-related epilepsy in Denmark.
Journal: Molecular genetics and metabolism reports
Published: August 01, 2022
Pacemaker Implantation in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3)-A Long-Term Follow-Up Study.
Journal: Frontiers in neurology
Published: December 30, 2021
Managing CLN2 disease: a treatable neurodegenerative condition among other treatable early childhood epilepsies.
Journal: Expert review of neurotherapeutics
Published: February 04, 2021
Discovery of a Potent Adenine-Benzyltriazolo-Pleuromutilin Conjugate with Pronounced Antibacterial Activity against MRSA.
Journal: Journal of medicinal chemistry
Published: December 16, 2020
Phenotypic heterogeneity and mosaicism in Xia-Gibbs syndrome: Five Danish patients with novel variants in AHDC1.
Journal: European journal of medical genetics
Published: December 07, 2020
Diagnosis, monitoring and treatment of tuberous sclerosis complex
Journal: Ugeskrift for laeger
Published: December 04, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026