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For: Gonçalves FG, Alves CAPF, Heuer B, Peterson J, Viaene AN, Reis Teixeira S, Martín-Saavedra JS, Andronikou S, Goldstein A, Vossough A. Primary Mitochondrial Disorders of the Pediatric Central Nervous System: Neuroimaging Findings. Radiographics 2020;40:2042-67. [PMID: 33136487 DOI: 10.1148/rg.2020200052] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 15.0] [Reference Citation Analysis]
Number Citing Articles
1 Okafor C, Kanekar S. Imaging of Microcephaly. Clin Perinatol 2022;49:693-713. [PMID: 36113930 DOI: 10.1016/j.clp.2022.04.004] [Reference Citation Analysis]
2 Nemoto K, Sano K, Sato S, Maeda Y, Murayama K, Takanashi J. A child with mitochondrial DNA deletion presenting diabetes mellitus as an initial symptom. Radiology Case Reports 2022;17:2915-2918. [DOI: 10.1016/j.radcr.2022.05.061] [Reference Citation Analysis]
3 Tierradentro-garcía LO, Zandifar A, Ullman NL, Venkatakrishna SSB, Kim JDU, Martin RJ, Alves CA, Sotardi S, Donahue MJ, Bhatia A. Imaging of Suspected Stroke in Children, From the AJR Special Series on Emergency Radiology. American Journal of Roentgenology. [DOI: 10.2214/ajr.22.27816] [Reference Citation Analysis]
4 Sahly AN, Buhas D, Myers KA. MT-TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy. Am J Med Genet A 2022. [PMID: 35920329 DOI: 10.1002/ajmg.a.62925] [Reference Citation Analysis]
5 Wei Y, Qian M, Yang Y. Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation. Neurol Sci 2022. [DOI: 10.1007/s10072-022-06305-3] [Reference Citation Analysis]
6 Serrallach BL, Orman G, Boltshauser E, Hackenberg A, Desai NK, Kralik SF, Huisman TAGM. Neuroimaging in cerebellar ataxia in childhood: A review. J Neuroimaging 2022. [PMID: 35749078 DOI: 10.1111/jon.13017] [Reference Citation Analysis]
7 Ventura N. Inherited neurometabolic diseases and the importance of imaging-based classification systems. Radiol Bras 2022;55:VII-VIII. [PMID: 35795600 DOI: 10.1590/0100-3984.2022.55.3e2-en] [Reference Citation Analysis]
8 Ventura N. Doenças neurometabólicas hereditárias e a importância das classificações baseadas em achados de imagem. Radiol Bras 2022;55:3-4. [DOI: 10.1590/0100-3984.2022.55.3e2] [Reference Citation Analysis]
9 Huisman TAGM, Kralik SF, Desai NK, Serrallach BL, Orman G. Neuroimaging of primary mitochondrial disorders in children: A review. J Neuroimaging 2022. [PMID: 35107193 DOI: 10.1111/jon.12976] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Uittenbogaard M, Sen K, Whitehead M, Brantner CA, Wang Y, Wong LJ, Gropman A, Chiaramello A. Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome. Front Cell Dev Biol 2021;9:767407. [PMID: 35004675 DOI: 10.3389/fcell.2021.767407] [Reference Citation Analysis]
11 Marco-Hernández AV, Tomás-Vila M, Montoya-Filardi A, Barranco-González H, Vilchez Padilla JJ, Azorín I, Smeyers Dura P, Monfort-Membrado S, Pitarch-Castellano I, Martínez-Castellano F. Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene. Clin Genet 2021. [PMID: 34842280 DOI: 10.1111/cge.14093] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Stokes JC, Bornstein RL, James K, Park KY, Spencer K, Vo K, Snell JC, Johnson BM, Morgan PG, Sedensky MM, Baertsch N, Johnson SC. Leukocyte proliferation mediates disease pathogenesis in the Ndufs4(KO) mouse model of Leigh syndrome.. [DOI: 10.1101/2021.11.11.468271] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Gayathri N, Deepha S, Sharma S. Diagnosis of primary mitochondrial disorders -Emphasis on myopathological aspects. Mitochondrion 2021;61:69-84. [PMID: 34592422 DOI: 10.1016/j.mito.2021.09.007] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Goldman-yassen AE, Dehkharghani S. Neuroimaging in Pediatric Stroke and Cerebrovascular Disease. Stroke 2021. [DOI: 10.36255/exonpublications.stroke.pediatricstroke.2021] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]