Congenital Mirror Movement Disorder Latest Advances

Germline Variant Call Accuracy in Whole Genome Sequence Data from Canine Formalin-Fixed Paraffin-Embedded Tissue Samples.

Journal: Genes

Published: September 24, 2025

Reply to: "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 22, 2025

Congenital mirror movements in a family: Outcomes associated with DCC mutations.

Journal: Journal of neurogenetics

Published: July 06, 2025

Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: June 24, 2025

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

Journal: Medicine

Published: June 09, 2025

EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 20, 2025

A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC.

Journal: Science signaling

Published: October 01, 2024

HABIT training in unilateral spastic cerebral palsy children having mirror movement disorder.

Journal: JPMA. The Journal of the Pakistan Medical Association

Published: July 19, 2024

NeuroLab 2.0: An Alternative Storyline Design Approach for Translating a Research-Based Summer Experience into an Advanced STEM+M Curriculum Unit that Supports Three-Dimensional Teaching and Learning in the Classroom.

Journal: Journal of STEM outreach

Published: June 05, 2024

Effect of constraint-induced movement therapy in reducing severity of mirror movements in children with unilateral spastic cerebral palsy.

Journal: JPMA. The Journal of the Pakistan Medical Association

Published: January 14, 2024

Laurin-Sandrow Syndrome: A Case Report and Review of Literature.

Journal: The journal of hand surgery Asian-Pacific volume

Published: August 15, 2022

Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes.

Journal: Cortex; a journal devoted to the study of the nervous system and behavior

Published: June 07, 2022

Congenital Mirror Movement Disorder Latest Advances

Find the Latest Research About Congenital Mirror Movement Disorder

Germline Variant Call Accuracy in Whole Genome Sequence Data from Canine Formalin-Fixed Paraffin-Embedded Tissue Samples.

Germline Variant Call Accuracy in Whole Genome Sequence Data from Canine Formalin-Fixed Paraffin-Embedded Tissue Samples.

Reply to: "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Reply to: "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Congenital mirror movements in a family: Outcomes associated with DCC mutations.

Congenital mirror movements in a family: Outcomes associated with DCC mutations.

Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder.

EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder.

A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC.

A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC.

HABIT training in unilateral spastic cerebral palsy children having mirror movement disorder.

HABIT training in unilateral spastic cerebral palsy children having mirror movement disorder.

NeuroLab 2.0: An Alternative Storyline Design Approach for Translating a Research-Based Summer Experience into an Advanced STEM+M Curriculum Unit that Supports Three-Dimensional Teaching and Learning in the Classroom.

NeuroLab 2.0: An Alternative Storyline Design Approach for Translating a Research-Based Summer Experience into an Advanced STEM+M Curriculum Unit that Supports Three-Dimensional Teaching and Learning in the Classroom.

Effect of constraint-induced movement therapy in reducing severity of mirror movements in children with unilateral spastic cerebral palsy.

Effect of constraint-induced movement therapy in reducing severity of mirror movements in children with unilateral spastic cerebral palsy.

Laurin-Sandrow Syndrome: A Case Report and Review of Literature.

Laurin-Sandrow Syndrome: A Case Report and Review of Literature.

Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes.

Mirror movements and callosal dysgenesis in a family with a DCC mutation: Neuropsychological and neuroimaging outcomes.