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CASE REPORT

CADASIL and multiple sclerosis: A case report of prolonged misdiagnosis

Keep up to date with the latest research on this topic with citation updates for this article.

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Chueh Lin Hsu, Piotr Iwanowski, Chueh Hsuan Hsu & Wojciech Kozubski. (2021) Genetic diseases mimicking multiple sclerosis. Postgraduate Medicine 133:7, pages 728-749.
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Articles from other publishers (5)

Julia Węgrzynek, Agnieszka Tomaszewska & Angelika Wawrzkiewicz-Witkowska. (2023) Patient with CADASIL – a diagnostic challenge. Annales Academiae Medicae Silesiensis 77, pages 151-157.
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Tehreem Arshad, Muhammad Jawad Hassan & Arsalan Ahmad. (2023) Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) with Rare Exon 7 Mutation in Pakistan: A Clinico-Genetic Correlation. Journal of Brown Hospital Medicine 2:4.
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Jinghan Hu, Jing Qian, Zhihui Che, Bin Tang, Yan Li, Qiang Gong & Xianzhen Lu. (2023) A novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL. Journal of Stroke and Cerebrovascular Diseases 32:8, pages 107208.
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Ayesha Khan, Vida Abedi, Jiang Li, Muhammad T. Malik, Megan Esch & Ramin Zand. (2020) CADASIL vs. Multiple Sclerosis: Is It Misdiagnosis or Concomitant? A Case Series. Frontiers in Neurology 11.
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Ilaria Di Donato, Silvia Bianchi, Nicola De Stefano, Martin Dichgans, Maria Teresa Dotti, Marco Duering, Eric Jouvent, Amos D. Korczyn, Saskia A. J. Lesnik-Oberstein, Alessandro Malandrini, Hugh S. Markus, Leonardo Pantoni, Silvana Penco, Alessandra Rufa, Osman Sinanović, Dragan Stojanov & Antonio Federico. (2017) Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects. BMC Medicine 15:1.
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