نتائج البحث

CADASIL Disease Discovery

• Source: CADASIL Disease Discovery

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Natural History Study of CADASIL

• Source: Natural History Study of CADASIL

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AusCADASIL: An Australian Cohort of CADASIL

• Authors : Prince of Wales Hospital, Sydney; John Hunter Hospital; St Vincent's Hospital - Sydney, Australia ...

• Source: AusCADASIL: An Australian Cohort of CADASIL

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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Study

• Authors : National Institute on Aging (NIA)

• Source: Unraveling the Early Phases of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

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Phenotypes Associated with NOTCH3 Cysteine-Sparing Mutations in Patients with Clinical Suspicion of CADASIL: A Systematic Review.

• Authors : Cao, Yuan¹ (AUTHOR) ; Zhang, Ding-Ding² (AUTHOR) ; Han, Fei¹ (AUTHOR)

• Source: International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 16, p8796. 14p.

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First report of a p.Cys484Tyr Notch3 mutation in a CADASIL patient with acute bilateral multiple subcortical infarcts-case report and brief review.

• Authors : Liu W; Department of Neurology II, Affiliated Hospital of Weifang Medical University, School of Clinical Medicine, Weifang Medical University, Weifang, China.; Zhang J

Subjects: CADASIL*/CADASIL*/CADASIL*/complications ; CADASIL*/CADASIL*/CADASIL*/diagnostic imaging ; CADASIL*/CADASIL*/CADASIL*/genetics

• Source: BMC neurology [BMC Neurol] 2024 Feb 26; Vol. 24 (1), pp. 77. Date of Electronic Publication: 2024 Feb 26.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Long-Term Treatment with the Calcitonin Gene-Related Peptide Receptor Antagonist Erenumab in CADASIL: Two Case Reports.

• Authors : Albanese, Maria^1,2 (AUTHOR) ; Pescini, Francesca^3,4 (AUTHOR) ; Di Bonaventura, Chiara⁵ (AUTHOR)

• Source: Journal of Clinical Medicine. Apr2024, Vol. 13 Issue 7, p1870. 8p.

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Adrenomedullin for CADASIL (AMCAD)

• Authors : Masafumi Ihara, Director of Neurology, National Cerebral and Cardiovascular Center

• Source: A Multicenter, Single-arm, Clinical Trial of Adrenomedullin for Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

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Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease.

• Authors : Mizuta I; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto 602-8566, Japan.; Nakao-Azuma Y

Subjects: CADASIL*/CADASIL*/CADASIL*/genetics ; Cerebral Small Vessel Diseases*; Adult

• Source: Biomolecules [Biomolecules] 2024 Jan 18; Vol. 14 (1). Date of Electronic Publication: 2024 Jan 18.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101596414 Publication Model: Electronic Cited Medium: Internet ISSN: 2218-273X

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CERebrolysin In CADASIL (CERICA)

• Authors : idv Datenanalyse & Versuchsplanung; XClinical GmbH

• Source: A Randomized, Double-blind, Single-centre, Two-period Cross-over, Placebo-controlled Trial on Safety and Efficacy in Patients With Genetically Proven CADASIL

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