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For: Isik E, Yilmaz S, Atik T, Aktan G, Onay H, Gokben S, Ozkinay F. The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathies. Neurol Sci 2020;41:3729-39. [DOI: 10.1007/s10072-020-04619-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Ocampo-chih C, Dennis H, Lall N, Pham N, Liang B, Verma S, Fresneda JN. PEBAT, an intriguing neurodegenerative tubulinopathy caused by a novel homozygous variant in TBCD; A case series and literature review. Pediatric Neurology 2022. [DOI: 10.1016/j.pediatrneurol.2022.11.006] [Reference Citation Analysis]
2 Bican R, Ferrante R, Hendershot S, Byars M, Lo W, Heathcock JC. Daily Outpatient Physical Therapy for a Toddler With a Neurodegenerative Disease: A Case Report. Pediatr Phys Ther 2022;34:261-7. [PMID: 35385464 DOI: 10.1097/PEP.0000000000000884] [Reference Citation Analysis]
3 Quitmann CM, Rust S, Reunert J, Biskup S, Fiedler B, Marquardt T. Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing. Child Neurol Open 2021;8:2329048X211034969. [PMID: 34423067 DOI: 10.1177/2329048X211034969] [Reference Citation Analysis]
4 Neuray C, Sultan T, Alvi JR, Franca MC, Assmann B, Wagner M, Canafoglia L, Franceschetti S, Rossi G, Santana I, Macario MC, Almeida MR, Kamate M, Parikh S, Elloumi HZ, Murphy D, Efthymiou S, Maroofian R, Houlden H. Early-onset phenotype of bi-allelic GRN mutations. Brain 2021;144:e22. [PMID: 33351065 DOI: 10.1093/brain/awaa414] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]