Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I.
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy. Neurology. 2002 Dec 10;59(11):1689-1693. (Discussed in Editorial)
Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I.
Ullrich disease: Collagen VI deficiency. EM suggests a new basis for muscular weakness. Neurology.2002 Sep 24;59(6):920-923. (Discussed in Highlight)
Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kellely RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP.
Posttranslational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature. 2002 Jul 25;418(6896):417-422.
Sugie K, Yamamoto A, Murayama K, Takahashi M, Mora M, Riggs JE, Oh SJ, Colomer J, Inturriaga C, Saitoh S, Byrne E, DiMauro S, Noanka I, Hirano M, Nishino I.
Clinicopathological features of genetically confirmed Danon disease. Neurology.2002 Jun 25;58(12):1773-1778.
Arikawa-Hirasawa E, Le AH, Nishino I, Nonaka I, Ho NC, Francomano CA, Govindraj P, Hassell JR, Devaney JM, Spranger J, Stevenson RE, Iannaccone S, Dalakas, MC, Yamada Y.
Structural and functional mutations of the Perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia. Am J Hum Genet. 2002 May;70(5):1368-1375.