Dragan Marjanovic

Holbaek, Denmark

Last Updated: 09/26/2026

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Found 16 publications

Programming in Vagus nerve stimulation therapy: Consensus from a Nordic Delphi Panel.

Programming in Vagus nerve stimulation therapy: Consensus from a Nordic Delphi Panel.

Journal: Seizure

Published: April 03, 2025

Clinical and molecular characterization of patients with YWHAG-related epilepsy.

Clinical and molecular characterization of patients with YWHAG-related epilepsy.

Journal: Epilepsia

Published: November 10, 2023

IRF2BPL as a novel causative gene for progressive myoclonus epilepsy.

IRF2BPL as a novel causative gene for progressive myoclonus epilepsy.

Journal: Epilepsia

Published: February 07, 2023

Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome.

Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 30, 2022

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications.

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications.

Journal: Brain : a journal of neurology

Published: January 13, 2022

4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy.

4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy.

Journal: Science translational medicine

Published: September 13, 2021

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.

Journal: Brain : a journal of neurology

Published: July 15, 2021

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood.

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood.

Journal: Neurology

Published: June 22, 2021

Utility of genetic testing for therapeutic decision-making in adults with epilepsy.

Utility of genetic testing for therapeutic decision-making in adults with epilepsy.

Journal: Epilepsia

Published: November 27, 2019

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Journal: Brain : a journal of neurology

Published: January 14, 2019

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 04, 2018

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 17, 2018

Showing 1-12 of 16

Last Updated: 09/26/2026