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Cited by in F6Publishing
For: Kalantari S, Brezzi B, Bracciamà V, Barreca A, Nozza P, Vaisitti T, Amoroso A, Deaglio S, Manganaro M, Porta F, Spada M. Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists. Orphanet J Rare Dis 2022;17:33. [PMID: 35109910 DOI: 10.1186/s13023-022-02179-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Di Giacomo R, Salsano E, Deleo F, Pastori C, Didato G, Stabile A, Ferrario R, Giovagnoli AR, Benzoni C, Sarro L, Visani E, Canafoglia L. Epileptic syndrome with myoclonus as manifestation of adult-onset CblC deficiency. J Neurol. [DOI: 10.1007/s00415-022-11129-4] [Reference Citation Analysis]
2 Wang S, Wang X, Xi J, Yang W, Zhu M. Case Report: A Case of Adult Methylmalonic Acidemia With Bilateral Cerebellar Lesions Caused by a New Mutation in MMACHC Gene. Front Neurol 2022;13:935604. [DOI: 10.3389/fneur.2022.935604] [Reference Citation Analysis]