ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
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Yoshihiko Saito | T. Kanda | I. Nonaka | I. Nishino | A. Iida | S. Noguchi | A. Ishiyama | S. Hayashi | H. Komaki | M. Mori-Yoshimura | Y. Oya | A. Nishikawa | M. Yamadera | H. Sakiyama | S. Fujikawa | Seigo Nakamura
[1] J. Lee,et al. Distal myopathy with ADSSL1 mutations in Korean patients , 2017, Neuromuscular Disorders.
[2] S. Han,et al. Electron Microscopy Pathology of ADSSL1 Myopathy , 2016, Journal of Clinical Neurology.
[3] I. Nishino,et al. Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders , 2016, Journal of Medical Genetics.
[4] T. Kishimoto,et al. Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene , 2016, Neuropathology : official journal of the Japanese Society of Neuropathology.
[5] I. Nonaka,et al. Hepatitis C virus infection in inclusion body myositis , 2016, Neurology.
[6] 최영철,et al. ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy , 2016 .
[7] I. Nonaka,et al. Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channels. , 2015, Human molecular genetics.
[8] S. Sandaradura,et al. Recent advances in nemaline myopathy , 2013, Current opinion in neurology.
[9] Volker Straub,et al. TREAT-NMD workshop: Pattern recognition in genetic muscle diseases using muscle MRI 25–26 February 2011, Rome, Italy , 2012, Neuromuscular Disorders.
[10] P. Laforêt,et al. Disorders of muscle lipid metabolism: Diagnostic and therapeutic challenges , 2010, Neuromuscular Disorders.
[11] I. Nishino,et al. State of the art in muscle lipid diseases , 2010, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
[12] J. Allsop,et al. Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy , 2005, Neuromuscular Disorders.
[13] Nan Li,et al. Molecular cloning and characterization of a novel muscle adenylosuccinate synthetase, AdSSL1, from human bone marrow stromal cells , 2005, Molecular and Cellular Biochemistry.
[14] L. Machesky,et al. Congenital myopathies: diseases of the actin cytoskeleton , 2004, The Journal of pathology.
[15] U. de Girolami,et al. Clinical course correlates poorly with muscle pathology in nemaline myopathy , 2003, Neurology.
[16] H. Fromm,et al. IMP, GTP, and 6-Phosphoryl-IMP Complexes of Recombinant Mouse Muscle Adenylosuccinate Synthetase* , 2002, The Journal of Biological Chemistry.
[17] Y. Xia,et al. The adenylosuccinate synthetase‐1 gene is activated in the hypertrophied heart , 2002, Journal of cellular and molecular medicine.
[18] A. Beggs,et al. Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments. , 2001, Trends in molecular medicine.
[19] J. Brucher,et al. Enzymes of the purine nucleotide cycle in muscle of patients with exercise intolerance , 1998, Muscle & nerve.
[20] O. Guicherit,et al. Molecular cloning and expression of a mouse muscle cDNA encoding adenylosuccinate synthetase. , 1991, The Journal of biological chemistry.