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Russell D’Aiello

affiliation not provided to SSRN

SCHOLARLY PAPERS

2

DOWNLOADS

127

TOTAL CITATIONS

0

Scholarly Papers (2)

1.

Developmental Trajectory of Individuals with Pelizaeus-Merzbacher Disease (PMD)

Number of pages: 32 Posted: 02 Jan 2026
affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, C.O.A.L.A (Center for diagnosis and treatment of 5eukodystrophies), affiliation not provided to SSRN, affiliation not provided to SSRN, Children’s Hospital of Philadelphia, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, McGill University, National Center of Neurology and Psychiatry, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, McGill University, National Center of Neurology and Psychiatry, affiliation not provided to SSRN, affiliation not provided to SSRN, University of Pennsylvania and University of Pennsylvania
Downloads 81 (809,932)

Abstract:

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Pelizaeus-Merzbacher Disease, developmental outcomes, disease progression, prognosis prediction, cohort stratification, clinical trial readiness

2.

Systemic Complications of Aicardi Goutières Syndrome Using Real World Data

Number of pages: 40 Posted: 12 Jun 2024
affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Children’s Hospital of Philadelphia, affiliation not provided to SSRN, Stanford University, Emory University, affiliation not provided to SSRN, Baylor College of Medicine, affiliation not provided to SSRN, University of Pennsylvania, University of Pennsylvania and affiliation not provided to SSRN
Downloads 46 (1,133,231)

Abstract:

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Aicardi Goutières Syndrome, leukodystrophy, clinical manifestations, interferonopathy, genotype