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For: Musumeci O, Barca E, Lamperti C, Servidei S, Comi GP, Moggio M, Mongini T, Siciliano G, Filosto M, Pegoraro E, Primiano G, Ronchi D, Vercelli L, Orsucci D, Bello L, Zeviani M, Mancuso M, Toscano A. Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients. Front Neurol 2019;10:160. [PMID: 30873109 DOI: 10.3389/fneur.2019.00160] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
Number Citing Articles
1 Ferreira CR, Martinelli D, Blau N. Clinical and biochemical footprints of inherited metabolic diseases. VI. Metabolic dermatoses. Mol Genet Metab 2021:S1096-7192(21)00756-3. [PMID: 34304991 DOI: 10.1016/j.ymgme.2021.07.005] [Reference Citation Analysis]
2 Sanna M, Borgo C, Compagnin C, Favaretto F, Vindigni V, Trento M, Bettini S, Comin A, Belligoli A, Rugge M, Bassetto F, Donella-Deana A, Vettor R, Busetto L, Milan G. White Adipose Tissue Expansion in Multiple Symmetric Lipomatosis Is Associated with Upregulation of CK2, AKT and ERK1/2. Int J Mol Sci 2020;21:E7933. [PMID: 33114687 DOI: 10.3390/ijms21217933] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Hamel J, Tawil R. Case Studies on the Genetic and Clinical Diagnosis of Facioscapulohumeral Muscular Dystrophy. Neurol Clin 2020;38:529-40. [PMID: 32703466 DOI: 10.1016/j.ncl.2020.03.003] [Reference Citation Analysis]
4 Chen KK, Ni LS, Yu WH. Madelung disease: A case report. World J Clin Cases 2021; 9(8): 1983-1988 [PMID: 33748250 DOI: 10.12998/wjcc.v9.i8.1983] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Ng YS, Lim AZ, Panagiotou G, Turnbull DM, Walker M. Endocrine manifestations and new developments in mitochondrial disease. Endocr Rev 2021:bnab036. [PMID: 34644386 DOI: 10.1210/endrev/bnab036] [Reference Citation Analysis]
6 Di Buono G, Romano G, Maienza E, Bonventre G, Gulotta L, Cupido F, Buscemi S, Agrusa A. Giant subcutaneous lipomatosis in Myoclonic Epilepsy with Ragged Red Fibers syndrome: The first literature report of "laparoscopic" excision. Asian J Surg 2020;43:855-6. [PMID: 32456962 DOI: 10.1016/j.asjsur.2020.04.012] [Reference Citation Analysis]
7 Orsucci D, Caldarazzo Ienco E, Rossi A, Siciliano G, Mancuso M. Mitochondrial Syndromes Revisited. J Clin Med 2021;10:1249. [PMID: 33802970 DOI: 10.3390/jcm10061249] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Montano V, Gruosso F, Simoncini C, Siciliano G, Mancuso M. Clinical features of mtDNA-related syndromes in adulthood. Arch Biochem Biophys 2021;697:108689. [PMID: 33227288 DOI: 10.1016/j.abb.2020.108689] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
9 Ticci C, Sicca F, Ardissone A, Bertini E, Carelli V, Diodato D, Di Vito L, Filosto M, La Morgia C, Lamperti C, Martinelli D, Moroni I, Musumeci O, Orsucci D, Pancheri E, Peverelli L, Primiano G, Rubegni A, Servidei S, Siciliano G, Simoncini C, Tonin P, Toscano A, Mancuso M, Santorelli FM. Mitochondrial epilepsy: a cross-sectional nationwide Italian survey. Neurogenetics 2020;21:87-96. [DOI: 10.1007/s10048-019-00601-5] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
10 López-Gallardo E, Cammarata-Scalisi F, Emperador S, Hernández-Ainsa C, Habbane M, Vela-Sebastián A, Bayona-Bafaluy MP, Montoya J, Ruiz-Pesini E. Mitochondrial DNA pathogenic mutations in multiple symmetric lipomatosis. Clin Genet 2020;97:731-5. [PMID: 31912494 DOI: 10.1111/cge.13701] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
11 Ji K, Zhao B, Lin Y, Wang W, Liu F, Li W, Zhao Y, Yan C. “Myo-neuropathy” is commonly associated with mitochondrial tRNALysine mutation. J Neurol 2020;267:3319-28. [DOI: 10.1007/s00415-020-10017-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Ticci C, Orsucci D, Ardissone A, Bello L, Bertini E, Bonato I, Bruno C, Carelli V, Diodato D, Doccini S, Donati MA, Dosi C, Filosto M, Fiorillo C, La Morgia C, Lamperti C, Marchet S, Martinelli D, Minetti C, Moggio M, Mongini TE, Montano V, Moroni I, Musumeci O, Pancheri E, Pegoraro E, Primiano G, Procopio E, Rubegni A, Scalise R, Sciacco M, Servidei S, Siciliano G, Simoncini C, Tolomeo D, Tonin P, Toscano A, Tubili F, Mancuso M, Battini R, Santorelli FM. Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases. J Clin Med 2021;10:2063. [PMID: 34065803 DOI: 10.3390/jcm10102063] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]