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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Differential diagnosis of Mendelian and mitochondrial disorders in patients with suspected multiple sclerosis
James D. Weisfeld‐Adams, Ilana B. Katz Sand, Justin M. Honce, et al.
Brain (2015) Vol. 138, Iss. 3, pp. 517-539
Open Access | Times Cited: 54

Showing 1-25 of 54 citing articles:

Immunopathology of multiple sclerosis
Calliope A. Dendrou, Lars Fugger, Manuel A. Friese
Nature reviews. Immunology (2015) Vol. 15, Iss. 9, pp. 545-558
Closed Access | Times Cited: 1984
Classification, diagnosis, and differential diagnosis of multiple sclerosis
Ilana Katz Sand
Current Opinion in Neurology (2015) Vol. 28, Iss. 3, pp. 193-205
Closed Access | Times Cited: 279
Differential diagnosis of suspected multiple sclerosis: an updated consensus approach
Andrew Solomon, Georgina Arrambide, Wallace Brownlee, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 8, pp. 750-768
Open Access | Times Cited: 87
Bassoon proteinopathy drives neurodegeneration in multiple sclerosis
Benjamin Schattling, Jan Broder Engler, Constantin Volkmann, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 6, pp. 887-896
Closed Access | Times Cited: 79
Mitochondria in neuroinflammation – Multiple sclerosis (MS), leber hereditary optic neuropathy (LHON) and LHON-MS
David Bargiela, Patrick F. Chinnery
Neuroscience Letters (2017) Vol. 710, pp. 132932-132932
Open Access | Times Cited: 67
The role of Sphingolipids in myelination and myelin stability and their involvement in childhood and adult demyelinating disorders
Paola Giussani, Alessandro Prinetti, Cristina Tringali
Journal of Neurochemistry (2020) Vol. 156, Iss. 4, pp. 403-414
Open Access | Times Cited: 57
Epigenetic Treatment of Neurodegenerative Disorders: Alzheimer and Parkinson Diseases
Michael H. Irwin, Walter H. Moos, Douglas V. Faller, et al.
Drug Development Research (2016) Vol. 77, Iss. 3, pp. 109-123
Closed Access | Times Cited: 57
Importance of cerebrospinal fluid analysis in the era of McDonald 2010 criteria: a German–Austrian retrospective multicenter study in patients with a clinically isolated syndrome
André Huss, Steffen Halbgebauer, Patrick Öckl, et al.
Journal of Neurology (2016) Vol. 263, Iss. 12, pp. 2499-2504
Open Access | Times Cited: 51
Diagnosis of multiple sclerosis: revisions of the McDonald criteria 2017 – continuity and change
Hans‐Peter Hartung, Jonas Graf, Orhan Aktaş, et al.
Current Opinion in Neurology (2019) Vol. 32, Iss. 3, pp. 327-337
Closed Access | Times Cited: 51
Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?
Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar, et al.
Multiple Sclerosis and Related Disorders (2018) Vol. 20, pp. 84-92
Closed Access | Times Cited: 40
Exploring medicinal plants as promising approaches for myasthenia Gravis and Multiple Sclerosis treatment: An emerging approach to new medicines
Aqleemul Islam, Kaisar Ahmad Bhat, Fayaz Ahmad, et al.
Elsevier eBooks (2025), pp. 117-154
Closed Access
Genetic diseases misdiagnosed as multiple sclerosis: observational study and review of literature
Daniele Mandia, Natalia Shor, Alise Carlson, et al.
Multiple Sclerosis and Related Disorders (2025), pp. 106439-106439
Closed Access
Common Clinical and Imaging Conditions Misdiagnosed as Multiple Sclerosis
Aksel Sıva
Neurologic Clinics (2017) Vol. 36, Iss. 1, pp. 69-117
Closed Access | Times Cited: 39
Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome
Tuğçe B. Balcı, Jorge Dávila, Denice Lewis, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2017) Vol. 177, Iss. 1, pp. 101-109
Closed Access | Times Cited: 35
Adult-Onset Genetic Central Nervous System Disorders Masquerading as Acquired Neuroinflammatory Disorders
Xavier Ayrignac, Clarisse Carra‐Dallière, Cécilia Marelli, et al.
JAMA Neurology (2022) Vol. 79, Iss. 10, pp. 1069-1069
Closed Access | Times Cited: 17
A Clinical Approach to the Differential Diagnosis of Multiple Sclerosis
Michel Toledano, Brian G. Weinshenker, Andrew Solomon
Current Neurology and Neuroscience Reports (2015) Vol. 15, Iss. 8
Closed Access | Times Cited: 33
Differential diagnosis and evaluation in pediatric inflammatory demyelinating disorders
Kevin Rostásy, Barbara Bajer-Kornek, Sunita Venkateswaran, et al.
Neurology (2016) Vol. 87, Iss. 9_Supplement_2
Open Access | Times Cited: 28
Differential Diagnosis of Suspected Multiple Sclerosis in Pediatric and Late-Onset Populations
Le H. Hua, Andrew Solomon, Sílvia Tenembaum, et al.
JAMA Neurology (2024) Vol. 81, Iss. 11, pp. 1210-1210
Closed Access | Times Cited: 3
Atypical inflammatory demyelinating lesions and atypical multiple sclerosis
Xavier Ayrignac, Clarisse Carra‐Dallière, Pierre Labauge
Revue Neurologique (2018) Vol. 174, Iss. 6, pp. 408-418
Closed Access | Times Cited: 24
Differential imaging of atypical demyelinating lesions of the central nervous system
Matteo Paoletti, Shaun Ivan Muzic, Francesca Marchetti, et al.
La radiologia medica (2021) Vol. 126, Iss. 6, pp. 827-842
Closed Access | Times Cited: 16
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing
Anna Rubegni, Carla Battisti, Alessandra Tessa, et al.
Journal of the Neurological Sciences (2017) Vol. 375, pp. 198-202
Closed Access | Times Cited: 20
CADASIL mimicking multiple sclerosis: The importance of clinical and MRI red flags
Stuti Joshi, Wayne Yau, Allan G. Kermode
Journal of Clinical Neuroscience (2016) Vol. 35, pp. 75-77
Closed Access | Times Cited: 18
Distribution of disease courses in familial vs sporadic multiple sclerosis
Maria Steenhof, Nete Munk Nielsen, Egon Stenager, et al.
Acta Neurologica Scandinavica (2018) Vol. 139, Iss. 3, pp. 231-237
Open Access | Times Cited: 16
Multiple sclerosis with atypical MRI presentation: Results of a nationwide multicenter study in 57 consecutive cases
Pekes Codjia, Xavier Ayrignac, Clarisse Carra‐Dallière, et al.
Multiple Sclerosis and Related Disorders (2018) Vol. 28, pp. 109-116
Closed Access | Times Cited: 15
Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis
Anthony Traboulsee, A. Dessa Sadovnick, Mary Joy Encarnacion, et al.
Human Genetics (2017) Vol. 136, Iss. 6, pp. 705-714
Closed Access | Times Cited: 14
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