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For: Caporali C, Signorini S, De Giorgis V, Pichiecchio A, Zuffardi O, Orcesi S. Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1-related syndrome. Eur J Paediatr Neurol 2018;22:336-9. [PMID: 29396177 DOI: 10.1016/j.ejpn.2018.01.007] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
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1 Stone DB, Ward EC, Knijnik SR, Bogaardt H, Elliott JM. Whiplash-Associated Dysphagia and Dysphonia: A Scoping Review. Dysphagia 2021;36:303-15. [PMID: 32445061 DOI: 10.1007/s00455-020-10137-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
2 Akol I, Gather F, Vogel T. Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective. Int J Mol Sci 2022;23:954. [PMID: 35055139 DOI: 10.3390/ijms23020954] [Reference Citation Analysis]
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4 Wong LC, Singh S, Wang HP, Hsu CJ, Hu SC, Lee WT. FOXG1-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms. Int J Mol Sci 2019;20:E4176. [PMID: 31454984 DOI: 10.3390/ijms20174176] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
5 Wong LC, Wu YT, Hsu CJ, Weng WC, Tsai WC, Lee WT. Cognition and Evolution of Movement Disorders of FOXG1-Related Syndrome. Front Neurol 2019;10:641. [PMID: 31316448 DOI: 10.3389/fneur.2019.00641] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
6 Craig CP, Calamaro E, Fong CT, Iqbal AM, Paciorkowski AR, Zhang B. Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review. Mol Cytogenet 2020;13:40. [PMID: 33632291 DOI: 10.1186/s13039-020-00506-1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Akaba Y, Takahashi S, Takeguchi R, Tanaka R, Nabatame S, Saitsu H, Matsumoto N. Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome. Clin Case Rep 2021;9:1711-5. [PMID: 33768920 DOI: 10.1002/ccr3.3883] [Reference Citation Analysis]
8 Tascini G, Dell'Isola GB, Mencaroni E, Di Cara G, Striano P, Verrotti A. Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative Review. Front Neurol 2022;13:817195. [PMID: 35299616 DOI: 10.3389/fneur.2022.817195] [Reference Citation Analysis]
9 Pringsheim M, Mitter D, Schröder S, Warthemann R, Plümacher K, Kluger G, Baethmann M, Bast T, Braun S, Büttel HM, Conover E, Courage C, Datta AN, Eger A, Grebe TA, Hasse-Wittmer A, Heruth M, Höft K, Kaindl AM, Karch S, Kautzky T, Korenke GC, Kruse B, Lutz RE, Omran H, Patzer S, Philippi H, Ramsey K, Rating T, Rieß A, Schimmel M, Westman R, Zech FM, Zirn B, Ulmke PA, Sokpor G, Tuoc T, Leha A, Staudt M, Brockmann K. Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice. Ann Clin Transl Neurol 2019;6:655-68. [PMID: 31019990 DOI: 10.1002/acn3.735] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]