English Journal

[Case report of a patient with Hashimoto's encephalopathy associated with Basedow's disease mimicking Creutzfeldt-Jakob disease].

Sakurai T1, Tanaka Y, Koumura A, Hayashi Y, Kimura A, Hozumi I, Yoneda M, Inuzuka T.
Brain and nerve = Shinkei kenkyū no shinpo.Brain Nerve.2008 May;60(5):559-65.
A 79-year-old female was admitted to our hospital because of unconsciousness and convulsion following mental deterioration. On admission, she exhibited myoclonic movement of the right side of the face and right fingers in addition to rigospasticity and tremors in the right arm and leg. Laboratory te
PMID 18516979

Clinical and clinico-pathologic characteristics of Shiba dogs with a deficiency of lysosomal acid beta-galactosidase: a canine model of human GM1 gangliosidosis.

Yamato O1, Masuoka Y, Yonemura M, Hatakeyama A, Satoh H, Kobayashi A, Nakayama M, Asano T, Shoda T, Yamasaki M, Ochiai K, Umemura T, Maede Y.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science.J Vet Med Sci.2003 Feb;65(2):213-7.
The present study was conducted to determine the clinical and clinico-pathologic characteristics of Shiba dogs with GM1 gangliosidosis, which is due to an autosomal recessively inherited deficiency of lysosomal acid beta-galactosidase activity. Clinical and clinico-pathological features were investi
PMID 12655116

Hereditary spastic paraplegia with thin corpus callosum and cataract: a clinical description of two siblings.

Okuda B1, Iwamoto Y, Tachibana H.
Acta neurologica Scandinavica.Acta Neurol Scand.2002 Oct;106(4):222-4.
We report two siblings with autosomal recessive hereditary spastic paraplegia and thin corpus callosum. These patients had a similar history of progressive spastic gait, followed by mental impairment in the second decade. In addition to rigospasticity, ataxia, and foot deformity, both patients had c
PMID 12225319

Japanese Journal

Clinical and Clinico-Pathologic Characteristics of Shiba Dogs with a Deficiency of Lysosomal Acid .BETA.-Galactosidase: A Canine Model of Human GM1 Gangliosidosis.