- Hereditary spastic paraplegia
- Leukodystrophy
- Leukoencephalopathy
- Multiple sclerosis
- White matter disease
Jennifer L. Orthmann Murphy, MD, PhD
About me
- Co-Director of the Age Span Fellowship in Multiple Sclerosis/Neuroinflammatory Disorders
- Assistant Professor of Neurology
My education and training
- Medical School: University of Pennsylvania School of Medicine
- Residency: University of Pennsylvania Health System
- Fellowship: Johns Hopkins Hospital
Spoken languages
Insurance accepted
- Aetna Advantra Cares D-SNP
- Aetna Advantra Credit Value
- Aetna Advantra Eagle HMO
- Aetna Advantra Eagle POS
- Aetna Advantra Premier Plus PPO
- Aetna Advantra Value
- Aetna Advantra Value Plus
- Aetna APCN Plus (Multi-Tier)
- Aetna Better Health Kids (CHIP) - DH Only
- Aetna Flexible Five
- Aetna Freedom Core
- Aetna Gold
- Aetna HMO
- Aetna Philly Prime
- Aetna POS
- Aetna PPO APCN
- Aetna Premier
- Aetna Premier Plus
- Aetna Savings Plus
- Aetna Signature Administrators
- Aetna Student Health Plan PPO
- Aetna Upfront Advantage
- First Health HMO
- First Health POS
- First Health PPO
- Meritain - Aramark (Other)
- Meritain - Aramark (Pennsylvania Premier Medical Plan)
- Centivo EPO
- Cigna Healthcare EPO
- Cigna Healthcare HMO
- Cigna Healthcare POS
- Cigna Healthcare PPO
- Claim Watcher (Homestead/ INDECs) Open Access
- Clover Health Choice
- Clover Health Choice Value PPO
- Clover Health Classic HMO
- Clover Health Value
- Devoted Health Choice Giveback Pennsylvania (PPO)
- Devoted Health Choice Pennsylvania (PPO)
- Devoted Health Choice Plus Pennsylvania (PPO)
- Devoted Health Core Pennsylvania (HMO)
- Devoted Health Dual Plus Pennsylvania (HMO D-SNP)
- Devoted Health Giveback Pennsylvania (HMO)
Locations
Penn Medicine hospital privileges
- Hospital of the University of Pennsylvania: Has privileges to treat patients in the hospital.
- Pennsylvania Hospital: Has privileges to treat patients in the hospital.
- Penn Presbyterian Medical Center: Has privileges to treat patients in the hospital.
Qualifications and experience
- Neurology, 2014
- Adult Polyglucosan Body Disease Research Foundation, International
- American Academy of Neurology, National
- American Neurological Association, National
- COMBINED Brain, International
- DEPARTMENT OF DEFENSE-CONGRESSIONALLY DIRECTED MEDICAL RESEARCH PROGRAMS, National
- DSMB for the trial "The use of technology to improve MS clinical, National
- European POLARIS Network Scientific Advisory Board, International
- Gliadelphia:, Local
- Global Leukodystrophy Initiative Clinical Trials Network, International
- Medical and Scientific Advisory Council, International
- Million Dollar Bike Ride, Penn Medicine Orphan Disease Center, International
- MS Australia, International
- National Multiple Sclerosis Society, National
- Society for Neuroscience, National
- UK MS Society, International
Treatments and conditions
Research
Publications
Kornbluh AB, Baldwin A, Fatemi A, Vanderver A, Adang LA, Van Haren K, Sampson J, Eichler FS, Sadjadi R, Engelen M, Orthmann-Murphy JL Practical Approach to Longitudinal Neurologic Care of Adults With X-Linked Adrenoleukodystrophy and Adrenomyeloneuropathy. , Neurology Genetics, 10(5): 2024,e200192
Adang LA, Bonkowsky JL, Boelens JJ, Mallack E, Ahrens-Nicklas R, Bernat JA, Bley A, Burton B, Darling A, Eichler F, Eklund E, Emrick L, Escolar M, Fatemi A, Fraser JL, Gaviglio A, Keller S, Patterson MC, Orchard P, Orthmann-Murphy J, Santoro JD, Schöls L, Sevin C, Srivastava IN, Rajan D, Rubin JP, Van Haren K, Wasserstein M, Zerem A, Fumagalli F, Laugwitz L, Vanderver A Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States , Cytotherapy, 26 (7): 2024,739-748
Sevagamoorthy A, Vanderver A, Fraser JL, Orthmann-Murphy J. Glial Origins of Inherited White Matter Disorders , Additional Perspectives on Glia in Cold Spring Harb Perspect Biol, 17(7): 2025,a041457
Baldwin A, Copeland J, Azage M, Dratch L, Johnson K, Paul RA, Amado DA, Baer M, Deik A, Elman LB, Guo M, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn CC, Tropea TF, Scherer SS, Shinohara RT, Hamilton RH, Ellis CA Disparities in genetic testing for neurologic disorders , Neurology, 102 (6): 2024,e209161
Dratch L, Azage M, Baldwin A, Johnson K, Paul RA, Bardakjian TM, Michon SC, Amado DA, Baer M, Deik AF, Elman LB, Gonzalez-Alegre P, Guo MH, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn C, Tropea TF, Scherer SS, Ellis CA Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts. , J Neurology , 271 (2): 2024,733-747
Felipe J.S. Jones and Jennifer Orthmann-Murphy Clinical Reasoning: A 26-year-old woman with chronic progressive gait dysfunction , Neurology , 103(7): 2024,e209830
Koch RL, Soler-Alfonso C, Kiely BT, Asai A, Smith AL, Bali DS, Kang PB, Landstrom AP, Akman HO, Burrow TA, Orthmann-Murphy JL, Goldman DS, Pendyal S, El-Gharbawy AH, Austin SL, Case LE, Schiffmann R, Hirano M, Kishnani PS. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource , Molecular Genetics and Metabolism, 138(3): 2023,107525
Helman G, Orthmann-Murphy JL, Vanderver A Approaches to diagnosis for individuals with a suspected inherited white matter disorder , Handb Clin Neurol, 204: 2024,21-35
Jones FJ, Elser H, Mendez A, Fraser JL, Orthmann-Murphy J. Neuroimage: Leukoencephalopathy With Calcifications and Cysts , Neurology, 103(9): 2024,e209936
Papapetropoulos S, Pontius A, Finger E, Karrenbauer V, Lynch DS, Brennan M, Zappia1 S, Koehler W, Schoels L, Hayer SN, Konno T, Ikeuchi T, Lund T, Orthmann-Murphy J, Eichler E and Wszolek ZK Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development , Frontiers in Neurology, 12: 2022,788168