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prednisolone and HMN (Hereditary Motor Neuropathy) Proximal Type I

prednisolone has been researched along with HMN (Hereditary Motor Neuropathy) Proximal Type I in 3 studies

Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.

Research Excerpts

ExcerptRelevanceReference
"In this population, with thorough screening and careful post-gene transfer management, replacement therapy with onasemnogene abeparvovec-xioi is safe and shows promise for early efficacy."1.56Gene Therapy for Spinal Muscular Atrophy: Safety and Early Outcomes. ( Alfano, LN; Bass, N; Broomall, E; Connolly, AM; Ginsberg, M; Goldstein, J; Iammarino, MA; Karingada, C; Lowes, LP; Mendell, JR; Miller, NF; Mosher, KA; Noritz, G; Powers, B; Rossman, I; Storey, MA; Tsao, CY; Waldrop, MA, 2020)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's3 (100.00)2.80

Authors

AuthorsStudies
Byon, JH1
Park, EH1
Lee, CH1
Feldman, AG1
Parsons, JA1
Dutmer, CM1
Veerapandiyan, A1
Hafberg, E1
Maloney, N1
Mack, CL1
Waldrop, MA1
Karingada, C1
Storey, MA1
Powers, B1
Iammarino, MA1
Miller, NF1
Alfano, LN1
Noritz, G1
Rossman, I1
Ginsberg, M1
Mosher, KA1
Broomall, E1
Goldstein, J1
Bass, N1
Lowes, LP1
Tsao, CY1
Mendell, JR1
Connolly, AM1

Other Studies

3 other studies available for prednisolone and HMN (Hereditary Motor Neuropathy) Proximal Type I

ArticleYear
Early Diagnosed Hirayama Disease with Unusual Symptoms Improved by Steroid Pulse Therapy.
    World neurosurgery, 2020, Volume: 140

    Topics: Cervical Cord; Drug Administration Schedule; Early Diagnosis; Glucocorticoids; Humans; Magnetic Reso

2020
Subacute Liver Failure Following Gene Replacement Therapy for Spinal Muscular Atrophy Type 1.
    The Journal of pediatrics, 2020, Volume: 225

    Topics: Chemical and Drug Induced Liver Injury; Female; Genetic Therapy; Glucocorticoids; Humans; Infant; Ma

2020
Gene Therapy for Spinal Muscular Atrophy: Safety and Early Outcomes.
    Pediatrics, 2020, Volume: 146, Issue:3

    Topics: Adenoviruses, Human; Age Factors; Alanine Transaminase; Aspartate Aminotransferases; Biological Prod

2020