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Publications by Mary-Louise Freckmann

Infantile Spasms Is Associated With Deletion of the MAGI2 Gene on Chromosome 7q11.23-Q21.11

American Journal of Human Genetics

English

Related publications

Infantile Spasms.

Archives of Disease in Childhood

English

CDKL5/STK9 Is Mutated in Rett Syndrome Variant With Infantile Spasms

Journal of Medical Genetics

English

Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A

English

Deletion of 22q11 Chromosome Is Associated With Postoperative Morbidity After Unifocalisation Surgery – CORRIGENDUM

Cardiology in the Young

Cardiovascular Medicine

English

Current Trends in the Treatment of Infantile Spasms

Neuropsychiatric Disease and Treatment

Biological Psychiatry

English

Hormonal Therapy With Vigabatrin Is Superior to Hormonal Therapy Alone in Infantile Spasms

Journal of Pediatrics

English

Heterozygous Deletion of the LRFN2 Gene Is Associated With Working Memory Deficits

European Journal of Human Genetics

English

High Frequency EEG Activity Associated With Ictal Events in an Animal Model of Infantile Spasms

English

Altered Default Mode Network on Resting-State fMRI in Children With Infantile Spasms

Frontiers in Neurology

English