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Cited by in F6Publishing
For: Gonzalez-Perez P, Smith C, Sebetka WL, Gedlinske A, Perlman S, Mathews KD. Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant). Neuromuscul Disord 2020;30:213-8. [PMID: 32115343 DOI: 10.1016/j.nmd.2020.01.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
Number Citing Articles
1 Findlay AR, Robinson SE, Poelker S, Seiffert M, Bengoechea R, Weihl CC. LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials. Ann Clin Transl Neurol 2022. [PMID: 36427278 DOI: 10.1002/acn3.51709] [Reference Citation Analysis]
2 Cervera-gaviria M, Enterría-rosales J, Juárez-vignon-whaley JJ, García-sánchez J, Treviño-velasco R, Cervera-gaviria J. Novel Radiological Brain Anomalies in a Patient with Congenital Muscular Dystrophy due to FKRP Mexican Founder Mutation c.1387A > G: Review of the Literature. J Pediatr Genet. [DOI: 10.1055/s-0041-1726470] [Reference Citation Analysis]