Matthew J Elrick

发表

Enterovirus D68 molecular and cellular biology and pathogenesis

A. Pekosz, P. Duggal, Matthew J Elrick, 2021, The Journal of biological chemistry.

Impaired proteolysis underlies autophagic dysfunction in Niemann-Pick type C disease.

A. Lieberman, Matthew J Elrick, Ting Yu, 2012, Human molecular genetics.

Apolipoprotein E genotype and neurological disease onset in Niemann–Pick disease, type C1

A. Lieberman, F. Porter, Matthew J Elrick, 2012, American journal of medical genetics. Part A.

Apolipoprotein E Genotype and Neurological Disease Onset in Niemann – Pick Disease , Type C 1

A. Lieberman, F. Porter, Matthew J Elrick, 2012 .

Conditional Niemann-Pick C mice demonstrate cell autonomous Purkinje cell neurodegeneration.

H. Paulson, V. Shakkottai, A. Lieberman, 2010, Human molecular genetics.

Clinical Subpopulations in a Sample of North American Children Diagnosed With Acute Flaccid Myelitis, 2012-2016

Eliza M. Gordon-Lipkin, T. Crawford, P. Duggal, 2019, JAMA pediatrics.

Acute Flaccid Myelitis-Keys to Diagnosis, Questions About Treatment, and Future Directions.

Matthew J Elrick, S. Hopkins, K. Messacar, 2019, JAMA pediatrics.

Heat Shock Protein Beta-1 Modifies Anterior to Posterior Purkinje Cell Vulnerability in a Mouse Model of Niemann-Pick Type C Disease

Zhaohui S. Qin, Z. Qin, A. Chinnaiyan, 2016, PLoS genetics.

De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.

C. Cytrynbaum, R. Weksberg, R. Kingston, 2020, American journal of human genetics.

Clinical Manifestations and Pathogenesis of Acute Necrotizing Encephalopathy: The Interface Between Systemic Infection and Neurologic Injury

A. Venkatesan, Matthew J Elrick, Abby Mandalla, 2022, Frontiers in Neurology.

Sphingosine, a product of ceramide hydrolysis, influences the formation of ceramide channels.

M. Colombini, Matthew J Elrick, S. Fluss, 2006, Biophysical journal.

Autophagy and Cell Autonomous Neurodegeneration in Niemann-Pick type C Disease

Matthew J Elrick, Matthew J. Elrick, 2013 .

Tau deletion exacerbates the phenotype of Niemann-Pick type C mice and implicates autophagy in pathogenesis.

A. Lieberman, Matthew J Elrick, C. D. Pacheco, 2009, Human molecular genetics.

Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy.

Kiely N. James, J. Rosenfeld, Alison M. Male, 2020, American journal of human genetics.

Acute flaccid myelitis: cause, diagnosis, and management

Eliza M. Gordon-Lipkin, Elizabeth M. Wells, R. Scheuermann, 2020, The Lancet.

Autophagic dysfunction in a lysosomal storage disorder due to impaired proteolysis

A. Lieberman, Matthew J Elrick, Matthew J. Elrick, 2013, Autophagy.

Impaired proteolysis underlies autophagic dysfunction in Niemann-Pick type C disease.

A. Lieberman, Matthew J Elrick, Ting Yu, 2012, Human molecular genetics.