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Page 1
Immunocytochemical study of nebulin in Duchenne muscular dystrophy.
Bonilla E, Miranda AF, Prelle A, Salviati G, Betto R, Zeviani M, Schon EA, DiMauro S, Rowland LP. Bonilla E, et al. Among authors: rowland lp. Neurology. 1988 Oct;38(10):1600-3. doi: 10.1212/wnl.38.10.1600. Neurology. 1988. PMID: 3419605
Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Among authors: rowland lp. Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339. Neurology. 1988. PMID: 3412580
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.
Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Wilhelmsen KC, et al. Among authors: rowland lp. Ann Neurol. 1996 Apr;39(4):507-20. doi: 10.1002/ana.410390413. Ann Neurol. 1996. PMID: 8619529 Review.
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn CD, Connolly AM, Verloes A, Guimarães J, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou GM, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M. Nishino I, et al. Among authors: rowland lp. Ann Neurol. 2000 Jun;47(6):792-800. Ann Neurol. 2000. PMID: 10852545
Melas: an original case and clinical criteria for diagnosis.
Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP. Hirano M, et al. Among authors: rowland lp. Neuromuscul Disord. 1992;2(2):125-35. doi: 10.1016/0960-8966(92)90045-8. Neuromuscul Disord. 1992. PMID: 1422200 Review.
312 results