T. Toda

Familial Creutzfeldt-Jakob Disease with a codon 200 mutation presenting as thalamic syndrome: diagnosis by single photon emission computed tomography using (99m)Tc-ethyl cysteinate dimer.

H. Nakazora, T. Kurihara, H. Nemoto, 2008, Internal medicine.

A case report of carotid body tumor.

T. Toda, Y. Noda, A. Sadi, 1997, Auris, nasus, larynx.

A patient who experienced thyroid storm complicated by rhabdomyolysis, deep vein thrombosis, and a silent pulmonary embolism: a case report

T. Yanagawa, Keigo Ashitani, Taro Umezu, 2013, BMC Research Notes.

Autoimmune polyglandular syndrome type 2 with myasthenia gravis crisis.

T. Ichijo, H. Nakazora, T. Kurihara, 2009, The neurologist.

Venous angioma with epilepsy.

H. Nakazora, H. Nemoto, T. Toda, 2006, Internal medicine.

Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient

Y. Fukuyama, T. Duprez, E. Kondo-Iida, 1999, Neuromuscular Disorders.

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

R. Cohn, T. Voit, B. Leube, 1999, Neuromuscular Disorders.

Triphasic waves in a patient with tuberculous meningitis

H. Nakazora, T. Kurihara, H. Nemoto, 2010, Journal of the Neurological Sciences.