Sugie K, Koori T, Yamamoto A, Ogawa M, Hirano M, Inoue K, Nonaka I, Nishino I.
Characterization of Danon disease in a man and his affected mother. Neuromuscul Disord. 2003 Nov;13(9):708-711.
Ishikawa H, Nonaka I, Nishino I.
Negative result in search for human alpha-dystrobrevin deficiency. Muscle Nerve.2003 Sep;28(3):387-388.
Nambu M, Kawabe K, Fukuda T, Okuno TB, Ohta S, Nonaka I, Sugie H, Nishino I.
A neonatal form of glycogen storage disease type IV with a nucleotide deletion in GBE1 gene. Neurology. 2003 Aug 12;61(3):392-394.
Kaneda D, Sugie K, Yamamoto A, Matsumoto H, Kato T, Nonaka I, Nishino I.
A novel form of autophagic vacuolar myopathy with late-onset and multi-organ involvement. Neurology. 2003 Jul 8;61(1):128-131.
Keira Y, Noguchi S, Minami N, Hayashi YK, Nishino I.
Localization of calpain 3 in human skeletal muscle and its alteration in limb-girdle muscular dystrophy 2A muscle. J Biochem. 2003 May;133(5):659-664.
Tagawa K, Ogawa M, Kawabe K, Yamanaka G, Matsumura T, Goto K, Nonaka I, Nishino I, Hayashi YK.
Protein and gene analysis of dysferlinopathy in a large group of Japanese muscular dystrophy patients. J Neurol Sci. 2003 Jul 15;211(1-2):23-28.
Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshiima S, Kudoh J, Hentati F, Nishino I.
Fukutin-related protein gene mutated in the original kindred with limb-girdle MD 2I. Neurology.2003 Apr 22;60(8):1341-1344. (当該号のEditorialsおよびHighlightsに採用されました)
Noguchi S, Tsukahara T, Fujita M, Kurokawa R, Tachikawa M, Toda T, Tsujimoto A, Arahata K, Nishino I.
cDNA microarray analysis of individual Duchnne muscular dystrophy patients. Hum Mol Genet. 2003 Mar 15;12(6):595-600. (当該号のcover articleに採用されました)