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Cited by in F6Publishing
For: Almeida MR, Elias I, Fernandes C, Machado R, Galego O, Santo G. NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype. Neurogenetics 2021. [PMID: 34851492 DOI: 10.1007/s10048-021-00679-w] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Moura J, Mendes Pinto C, Pinto P, Santos E. Inflammatory Optic Neuropathy as a Presenting Feature of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. The Neurohospitalist 2022. [DOI: 10.1177/19418744221132677] [Reference Citation Analysis]
2 Mönkäre S, Kuuluvainen L, Schleutker J, Myllykangas L, Pöyhönen M. Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Acta Neuro Scandinavica. [DOI: 10.1111/ane.13703] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]