Laurence E. Walsh

Pediatric Neurology | Neurology

1701 N Senate Blvd
Indianapolis, IN 46202

Last Updated: 09/26/2026

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Found 33 publications

Recurrent Autoimmune Encephalitis in a Patient With Autoimmune Polyendocrine Syndrome Type 1.

Recurrent Autoimmune Encephalitis in a Patient With Autoimmune Polyendocrine Syndrome Type 1.

Journal: Case reports in critical care

Published: February 13, 2026

Delayed focal seizures following gunshot wound to the head in a child with minimal initial sequelae.

Delayed focal seizures following gunshot wound to the head in a child with minimal initial sequelae.

Journal: Radiology case reports

Published: August 22, 2024

Electroconvulsive therapy in new onset refractory status epilepticus (NORSE) in a pediatric patient.

Electroconvulsive therapy in new onset refractory status epilepticus (NORSE) in a pediatric patient.

Journal: Brain stimulation

Published: May 01, 2024

Participant-reported personal utility of genetic testing for Parkinson's disease and interest in clinical trial participation.

Participant-reported personal utility of genetic testing for Parkinson's disease and interest in clinical trial participation.

Journal: NPJ Parkinson's disease

Published: April 25, 2024

Magnetic resonance imaging enhancement of spinal nerve roots in a boy with X-linked adrenoleukodystrophy before diagnosis of chronic inflammatory demyelinating polyneuropathy.

Magnetic resonance imaging enhancement of spinal nerve roots in a boy with X-linked adrenoleukodystrophy before diagnosis of chronic inflammatory demyelinating polyneuropathy.

Journal: Radiology case reports

Published: August 22, 2023

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Journal: NPJ genomic medicine

Published: August 16, 2023

Readiness for Parkinson's disease genetic testing and counseling in patients and their relatives in urban settings in the Dominican Republic.

Readiness for Parkinson's disease genetic testing and counseling in patients and their relatives in urban settings in the Dominican Republic.

Journal: NPJ Parkinson's disease

Published: March 20, 2023

Primary Erythromelalgia Treated With 10% Capsaicin Cream: A Case Report and a 10-Year Follow-Up.

Primary Erythromelalgia Treated With 10% Capsaicin Cream: A Case Report and a 10-Year Follow-Up.

Journal: Cureus

Published: August 24, 2022

A 9.8 Mb deletion at 7q31.2q31.31 downstream of FOXP2 in an individual with speech and language impairment suggests a possible positional effect.

A 9.8 Mb deletion at 7q31.2q31.31 downstream of FOXP2 in an individual with speech and language impairment suggests a possible positional effect.

Journal: Clinical case reports

Published: May 31, 2022

Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.

Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.

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

Published: March 05, 2021

Longitudinal MRI brain findings in the R1349Q pathogenic variant of CACNA1A.

Longitudinal MRI brain findings in the R1349Q pathogenic variant of CACNA1A.

Journal: Radiology case reports

Published: February 04, 2021

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.

Journal: American journal of human genetics

Published: January 28, 2021

Showing 1-12 of 33

Last Updated: 09/26/2026