T. Niiyama

发表

Multiple episodes of thrombosis in a patient with Becker muscular dystrophy with marked expression of utrophin on the muscle cell membrane

K. Arimura, M. Nakagawa, M. Osame, 1999, Acta Neuropathologica.

Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease

M. Osame, I. Higuchi, A. Saito, 2002, Muscle & nerve.

Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Osame, I. Higuchi, 2006, Muscle & nerve.

Dystrophin-related protein in Becker muscular dystrophy.

M. Nakagawa, M. Osame, I. Higuchi, 1994, Internal medicine.

An autopsy case of peripheral neuroepithelioma in posterior mediastinum with p53 point mutation.

M. Nakagawa, M. Osame, K. Mizuno, 1998, Internal medicine.

Skeletal muscle abnormalities in two patients with dystonia

K. Arimura, M. Osame, I. Higuchi, 2002, Acta Neuropathologica.

Hermansky-Pudlak syndrome with a novel mutation.

K. Arimura, M. Osame, W. Matsuyama, 2005, Internal medicine.

Accumulation of mitochondrial ATP synthase subunit c in muscle in a patient with neuronal ceroid lipofuscinosis (late infantile form)

J. Ezaki, E. Kominami, M. Osame, 1997, Acta Neuropathologica.

Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, T. Hashiguchi, 2003, Acta Neuropathologica.

Frameshift mutation in the collagen VI gene causes Ullrich's disease

K. Arimura, M. Nakagawa, T. Hashiguchi, 2001, Annals of neurology.

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, M. Osame, 2003, Neuromuscular Disorders.

Microvascular endothelial abnormality in skeletal muscle from a patient with gastric cancer without dermatomyositis

K. Arimura, M. Nakagawa, M. Osame, 2000, Acta Neuropathologica.

Expression of thrombomodulin, caveolin‐3, and desmin on muscle fibers in neuromuscular diseases

M. Osame, I. Higuchi, I. Maruyama, 1999, Muscle & nerve.

Characteristic Expression of Thrombomodulin in the Muscle Sarcoplasm in Patients with the Acute Phase of Rhabdomyolysis

M. Osame, I. Higuchi, M. Inose, 2000, European Neurology.

An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy

K. Arimura, M. Osame, I. Higuchi, 2000, Muscle & nerve.

Statistically significant differences in the number of CD24 positive muscle fibers and satellite cells between sarcoglycanopathy and age-matched Becker muscular dystrophy patients.

K. Arimura, M. Nakagawa, M. Osame, 1999, Internal medicine.

Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution

M. Nakagawa, M. Osame, I. Higuchi, 1999, Journal of Human Genetics.

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease

I. Maruyama, K. Arimura, M. Nakagawa, 2002, Acta Neuropathologica.

Diagnosis of dystrophinopathy by skin biopsy

M. Osame, I. Higuchi, T. Matsumura, 2002, Muscle & nerve.

Induction of apoptosis signal regulating kinase 1 (ASK1) after spinal cord injury in rats: possible involvement of ASK1-JNK and -p38 pathways in neuronal apoptosis.

K. Yone, T. Sakou, T. Niiyama, 1999, Journal of neuropathology and experimental neurology.