Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I.
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1). Neuromuscul Disord.2008 Dec;18(12):959-961. Epub 2008 Oct 25.
Ohkuma A, Nonaka I, Malicdan MC, Noguchi S, Nomura K, Sugie H, Hayashi YK, Nishino I.
Distal lipid storage myopathy due to PNPLA2 mutation. Neuromuscul Disord. 2008 Aug;18(8):671-674. Epub 2008 Jul 26.
Kawahara G, Ogawa M, Okada M, Malicdan MCV, Goto Y, Hayshi YK, Noguchi S, Nishino I.
Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytes. Muscle Nerve. 2008 Sep;38(3):1192-1195.
Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I.
Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM. Physiol Genomics. 2008 Sep 17;35(1):106-115. Epub 2008 Jul 15.Affixin activates Rac1 via betaPIX in C2C12 myoblast.
Matsuda C, Kameyama K, Suzuki A, Mishima W, Yamaji S, Okamoto H, Nishino I, Hayashi Y.
Affixin activates Rac1 via betaPIX in C2C12 myoblast. FEBS Lett. 2008 Apr 9;582(8):1189-1196. Epub 2008 Mar 4.
Oishi M, Miki K, Morita A, Fujioka K, Aoki S, Nishino I, Nonaka I, Goto Y, Mizutani T.
Mitochondrial encephaolopathy associated with diabetes mellitus, cataract, and corpus callosum atrophy. Intern Med. 2008;47(5):441-444. Epub 2008 Mar 3.
Tanabe T, Fukusaki M, TeraoY, Yamashita K, Sumikawa K, Mukaida K, Ibarra CA, Nishino I.
Malignant hyperthermia susceptibility diagnosed with a family-specific ryanodine receptor gene type 1 mutation. J Anesth. 2008;22(1):70-73. Epub 2008 Feb 27.
Okahashi S, Ogawa G, Suzuki M, Ogata K, Nishino I, Kawai M.
Asymptomatic sporadic dysferlinopathy presenting with elevation of serum creatine kinase. Typical distribution of muscle involvement shown by MRI but not by CT. Intern Med. 2008;47(5):441-444. Epub 2008 Mar 3.
Tunon T, Guerrero D, Urchaga A, Nishino I, Ayuso T, Matsuda Y, Caballero MC, Berj?n J, Imizcoz MA.
Danon disease: A novel Lamp-2 gene mutation in a family with four affected members. Neuromuscul Disord. 2008 Feb;18(2):167-174. Epub 2007 Dec 3.
Mitsuhashi H, Futai E, Sasagawa N, Hayashi YK, Nishino I, Ishiura S.
Csk-homologous kinase interacts with SHPS-1 and enhances neurite outgrowth of PC12 cells. J Neurochem. 2008 Apr;105(1):101-112. Epub 2007 Nov 12.
Takahashi N, Shimada T, Ishibashi Y, Yoshitomi H, Oyake N, Murakami Y, Nishino I, Nonaka I, Goto YI, Kitamura J.
Marked left ventricular hypertrophy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Int J Cardiol. 2008 Oct 13;129(3):e77-e80. Epub 2007 Sep 25.
Sato I, Wu S, Ibarra M CA, Hayashi YK, Fujita H, Tojo M, Oh SJ, Nonaka I, Noguchi S, Nishino I.
Congenital neuromuscular disease with uniform type 1 fiber associated with RYR1 mutation. Neurology.2008 Jan 8;70(2):114-22. Epub 2007 May 30. (世界で初めて、先天性全タイプ1線維病の原因を明らかにしました)
(当該号の"Highlights" および "Editorial"で取り上げられました)