S. Araki

D. Selkoe, C. Masters, M. Benson, 1999, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Hydrocephalus, corneal opacities, deafness, valvular heart disease, deformed toes and leptomeningeal fibrous thickening in adult siblings: a new syndrome associated with‐glucocerebrosidase deficiency and a mosaic population of storage cells

E. Uyama, M. Naito, M. Owada, 1992, Acta neurologica Scandinavica.

Structure of the mouse serum amyloid P component gene.

S. Nishiguchi, S. Araki, K. Shimada, 1988, Biochemical and biophysical research communications.

Nomenclature of amyloid and amyloidosis

G. Glenner, M. Kazatchkine, M. Benson, 1998 .

[Familial amyloidotic polyneuropathy].

S. Araki, 1990, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Correlative study of the incidence of opaque, necrotic and regenerative fibers in Duchenne dystrophy

T. Miike, M. Uchino, S. Araki, 2004, Acta Neuropathologica.

High single-dose alternate-day corticosteroid regimens in treatment of polymyositis

M. Uchino, S. Araki, O. Yoshida, 2004, Journal of Neurology.

Synthesis of acylated SOD derivatives which bind to the biomembrane lipid surface and dismutate extracellular superoxide radicals

Y. Morino, T. Utsumi, M. Inoue, 1988, FEBS letters.

Disturbed metabolism of glucose and related hormones in familial amyloidotic polyneuropathy: hypersensitivities of the autonomic nervous system and therapeutic prevention.

M. Hirota, T. Nakagawa, A. Miyazaki, 1991, Journal of the autonomic nervous system.

Lhermitte's sign and reflex tonic spasm in demyelinating diseases with special reference to their localizing value.

S. Araki, Y. Kuroiwa, 1963, Kyushu journal of medical science.

Ocular microangiopathy in familial amyloidotic polyneuropathy, type I

Y. Ando, S. Araki, E. Ando, 2004, Graefe's Archive for Clinical and Experimental Ophthalmology.

Role of variant prealbumin in the pathogenesis of familial amyloidotic polyneuropathy: fate of normal and variant prealbumin in the circulation.

Y. Morino, M. Inoue, A. Miyazaki, 1989, Archives of biochemistry and biophysics.

Noninvasive cardiovascular findings in familial amyloid polyneuropathy.

S. Araki, T. Sawayama, T. Kurihara, 1978, British heart journal.

ACUTE DEMYELINATING DISEASE COMPLICATING HERPES ZOSTER

Y. Toyokura, D. Mcalpine, S. Araki, 1959, Journal of neurology, neurosurgery, and psychiatry.

The Electroencephalogram in Acute Cerebrovascular Disease: Correlative studies between EEG and clinical pictures

S. Araki, A. Terao, K. Morimoto, 1974, Folia psychiatrica et neurologica japonica.

Myxoedematous polyneuropathy: a light and electron microscopic study of the peripheral nerve and muscle.

S. Araki, T. Shirabe, A. Terao, 1975, Journal of neurology, neurosurgery, and psychiatry.

Centronuclear Myopathy: A Light and Electron Microscopic Study and a Review of the Literature

S. Araki, T. Shirabe, A. Terao, 1973, Folia psychiatrica et neurologica japonica.

Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy.

S. Araki, K. Shimada, S. Mita, 1986, Molecular biology & medicine.

Changed affinity of apolipoprotein AII to high density lipoprotein (HDL) in patients with familial amyloidotic polyneuropathy (FAP) type I.

Y. Ando, A. Miyazaki, S. Araki, 1994, Biochimica et biophysica acta.

Minamata disease: an unusual neurological disorder caused by contaminated fish.

D. Mcalpine, S. Araki, 1958, Lancet.

[Epidemiologic study of multiple sclerosis, myasthenia gravis and polymyositis in the city of Kumamoto, Japan].

M. Uchino, S. Araki, O. Yoshida, 1983, Rinsho shinkeigaku = Clinical neurology.

Familial amyloidotic polyneuropathy type 1 in Kumamoto, Japan: a clinicopathologic, histochemical, immunohistochemical, and ultrastructural study.

Y. Kimura, S. Araki, K. Takahashi, 1991, Human pathology.

Transthyretin-related familial amyloidotic polyneuropathy—Progress in Kumamoto, Japan (1967–2010)—

Y. Ando, S. Araki, 2010, Proceedings of the Japan Academy. Series B, Physical and biological sciences.

Nomenclature of amyloid fibril proteins. Report from the meeting of the98. Part 1 [editorial]

D. Selkoe, C. Masters, R. Kyle, 1999 .

[Potassium permanganate reaction in amyloidosis].

S. Araki, S. Tawara, M. Nagamine, 1982, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Transthyretin and familial amyloidotic polyneuropathy.

Y. Ando, S. Araki, M. Ando, 1993, Internal medicine.

Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I.

F. Tashiro, K. Yamamura, M. Naito, 1991, The American journal of pathology.

Amyloid and Amyloidosis

S. Araki, T. Isobe, F. Uchino, 1988 .

Herpes Simplex Encephalitis: A light and electron microscopic study in a fatal case

S. Araki, A. Terao, Teruo Shirabe, 1973, Folia psychiatrica et neurologica japonica.

ATYPICAL PROGRESSIVE MUSCULAR ATROPHY

S. Araki, Y. Kuroiwa, H. Iwashita, 1966 .

Circulating autoantibody to muscle protein in a patient with paraneoplastic myositis and colon cancer.

S. Araki, T. Kumamoto, H. Ueyama, 1992, European neurology.

Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA

T. Tsuzuki, S. Araki, K. Shimada, 1986, Neurology.

Polyneuritic amyloidosis in a Japanese family.

M. Ohta, S. Araki, Y. Kuroiwa, 1968, Archives of neurology.

Familial amyloidotic polyneuropathy: Report of patients heterozygous for the transthyretin Gly42 gene

T. Murakami, S. Araki, S. Maruyama, 1992, Annals of neurology.

Experiences with metastatic neoplasms involving the spinal cord

R. Terry, A. Hirano, K. Barron, 1959, Neurology.

Minamata Disease: Late Effects of an Unusual Neurological Disorder Caused by Contaminated Fish

D. Mcalpine, S. Araki, 1959 .

Role of autonomic nerve functions in patients with familial amyloidotic polyneuropathy as analyzed by laser doppler flowmetry, capsule hydrograph, and cardiographic R–R interval

Y. Ando, S. Araki, T Kano, 1992, Muscle & nerve.

[Diabetic amyotrophy].

S. Araki, T. Kumamoto, H. Ueyama, 1991, Nihon rinsho. Japanese journal of clinical medicine.

The clinical diagnosis of McArdle's disease

R. Lovelace, L. Rowland, S. Araki, 1966, Neurology.

Progressing ischemic stroke in a homozygote with variant antithrombin III.

M. Uchino, E. Uyama, Y. Hashimoto, 1989, Stroke.

INTERLEUKIN-2 RECEPTOR LEVELS INDICATING RELAPSE IN MULTIPLE SCLEROSIS

S. Araki, T. Kumamoto, Keiko Adachi, 1989, The Lancet.

Transgenic mouse model of familial amyloidotic polyneuropathy type I: its production, biological features, and usefulness.

K. Yamamura, S. Araki, S. Yi, 1995, Laboratory animal science.

Quantitative detection of a variant prealbumin associated with type 1 familial amyloidotic polyneuropathy (Japanese type) by high performance liquid chromatography.

S. Tanase, Y. Morino, S. Araki, 1987, Clinica chimica acta; international journal of clinical chemistry.

[An adult case of Chédiak-Higashi syndrome with parkinsonism and marked atrophy of the central nervous system].

O. Doi, E. Uyama, S. Araki, 1991, Rinshō shinkeigaku Clinical neurology.

Optic atrophy, neural deafness, and distal neurogenic amyotrophy; report of a family with two affected siblings.

S. Araki, Y. Kuroiwa, H. Iwashita, 1970, Archives of neurology.

A novel transthyretin mutation associated with familial amyloidotic polyneuropathy.

S. Araki, K. Shimada, S. Onodera, 1992, Biochemical and biophysical research communications.

[A case report of Behçet's disease with intracranial hypertension due to superior sagittal sinus thrombophlebitis].

M. Uchino, E. Uyama, S. Nishiguchi, 1987, Rinsho shinkeigaku = Clinical neurology.

[An autopsy case of malignant melanoma possibly originating in the sphenoid sinus].

E. Uyama, K. Eto, S. Araki, 1988, Rinshō shinkeigaku Clinical neurology.

The 1990 Guidelines for Nomenclature and Classification of Amyloid and Amyloidosis

G. Glenner, M. Benson, P. Westermark, 1991 .

PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY

S. Araki, Y. Minamishima, A. Sumiyoshi, 1985 .

Progressive multifocal leukoencephalopathy. A case report with special reference to SV40 etiology.

S. Araki, Y. Minamishima, A. Sumiyoshi, 1985, Acta pathologica japonica.

Cloning and sequence analysis of cDNA for human prealbumin.

S Mita, S. Araki, K. Shimada, 1984, Biochemical and biophysical research communications.

Genetic basis for familial amyloidotic polyneuropathy

S. Araki, K. Shimada, S. Maeda, 1986, BioEssays : news and reviews in molecular, cellular and developmental biology.

Localization and characterization of dystrophin in muscle biopsy specimens from Duchenne muscular dystrophy and various neuromuscular disorders

T. Miike, S. Araki, M. Uchino, 1989, Muscle & nerve.

Electrophoretic studies of muscle proteins in Duchenne muscular dystrophy and other neuromuscular disorders--with special reference to the change of dystrophin.

T. Miike, M. Uchino, S. Araki, 1989, Japanese journal of medicine.

Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization

N. Niikawa, Y. Jinno, S. Araki, 1986, Japanese Journal of Human Genetics.

Contracture in McArdle's disease. Stability of adenosine triphosphate during contracture in phosphorylase-deficient human muscle.

L. Rowland, S. Araki, P. Carmel, 1965, Archives of neurology.

F. Tashiro, K. Yamamura, Kiyoshi Takahashi, 1991 .

Pathology of Familial Amyloidotic Polyneuropathy Occurring in Kumamoto

Y. Kimura, Kiyoshi Takahashi, S. Araki, 1988 .

Type I familial amyloidotic polyneuropathy (Japanese type)

S. Araki, 1984, Brain and Development.

Pathology of familial amyloidotic polyneuropathy with TTR Met 30 in Kumamoto, Japan

S. Araki, S. Yi, 2000, Neuropathology : official journal of the Japanese Society of Neuropathology.

Perturbation of glucose metabolism in familial amyloidotic polyneuropathy

M. Inoue, Y. Ando, A. Miyazaki, 1990, Annals of neurology.

Studies on the Fate of Normal and Variant Prealbumin in the Circulation

Y. Morino, M. Inoue, A. Miyazaki, 1988 .

Genetic Expression of a Variant Prealbumin in Typical and Late-Onset Japanese Family with Familial Amyloidotic Polyneuropathy

S. Araki, S. Mita, S. Yi, 1988 .

Clinical Investigations of Autonomic Heart Regulation and Renal Function of Familial Amyloidotic Polyneuropathy

Y. Kimura, S. Araki, Y. Horio, 1986 .

Amino acids of serum and urine in familial amyloidotic polyneuropathy.

S. Araki, T. Inokuchi, S. Mawatari, 1970, Archives of neurology.

Elevated soluble interleukin‐2 receptor levels in patients with active multiple sclerosis

S. Araki, T. Kumamoto, Keiko Adachi, 1990, Annals of neurology.

[Blue-rubber-bleb-nevus syndrome presented vascular dementia and chronic DIC--a case report].

M. Uchino, E. Uyama, K. Eto, 1989, Rinsho shinkeigaku = Clinical neurology.

Clinical Application of Somatosensory Cerebral Evoked Response for the Localization and the Level Diagnosis of Neuronal Lesions

S. Araki, A. Terao, 1975, Folia psychiatrica et neurologica japonica.

Periodic EEG Patterns Observed in Two Cases With Partial Seizures

S. Araki, T. Shirabe, A. Terao, 1977, Folia psychiatrica et neurologica japonica.

[Familial dystonia with atrophy of the putamen and caudate nuclei detected by CT scan--biochemical study of catecholamine metabolism].

S. Araki, S. Kawasaki, T. Hirase, 1983, Rinsho shinkeigaku = Clinical neurology.

[An adult case of congenital Horner's syndrome with heterochromia iridis--with special reference to alteration of Horner's sign associated with development].

E. Uyama, S. Araki, K. Adachi, 1989, Rinshō shinkeigaku Clinical neurology.

Amyloid protein and amyloidosis.1.Classification of amyloidosis.

S. Araki, 1993 .

Familial occurrence of migraine with a hemiplegic syndrome and cerebellar manifestations

M. Ohta, S. Araki, Y. Kuroiwa, 1967, Neurology.

Cerebrospinal fluid proteins in muscular dystrophy patients

S. Araki, T. Hirase, 1984, Brain & development (Tokyo. 1979).

Prevalence studies of multiple sclerosis, myasthenia gravis, and myopathies in Kumamoto district, Japan.

M. Uchino, S. Araki, T. Kumamoto, 1987, Neuroepidemiology.

[Clinical, pathophysiological, and therapeutic studies on familial amyloidotic polyneuropathy (author's transl)].

T. Kuribayashi, S. Araki, T. Kurihara, 1980, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

[Rapid prenatal diagnosis of familial amyloidotic polyneuropathy using DNA amplification].

S. Nishiguchi, S. Araki, K. Shimada, 1990, Rinshō shinkeigaku Clinical neurology.

[Review of clinical records and therapeutic trials to familial amyloidotic polyneuropathy--study of 50 cases in Kumamoto (1967-1984)].

S. Araki, Y. Takaba, A. Nakashima, 1986, Rinsho shinkeigaku = Clinical neurology.

[Familial amyloidotic polyneuropathy: review of the 20 year's study and prospective view].

S. Araki, 1986, Rinshō shinkeigaku Clinical neurology.

[Therapeutic effects of dimethyl sulfoxide on the urinary proteins of patients with familial amyloidotic polyneuropathy].

S. Araki, M. Tsuruoka, S. Tawara, 1982, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Early involvement of motor nerve dysfunction in atypical cases with familial amyloidotic polyneuropathy (FAP) type I.

Y. Ando, S. Araki, S. Watanabe, 1993, Muscle & nerve.

[Pathological study of familial primary amyloidosis with peripheral and autonomic nervous disorders as a main symptom, with special reference to 2 autopsy cases and literature review].

S. Araki, Y. Kuroiwa, S. Mawatari, 1969, Shinkei kenkyu no shimpo. Advances in neurological sciences.

Analyses of prealbumin mRNAs in individuals with familial amyloidotic polyneuropathy.

S. Araki, K. Shimada, S. Mita, 1986, Journal of biochemistry.

CO2 laser‐induced pain‐related somatosensory evoked potentials in peripheral neuropathies: Correlation between electrophysiological and histopathological findings

R. Kakigi, H. Shibasaki, A. Ikeda, 1991, Muscle & nerve.

[A case of central alveolar hypoventilation syndrome with a localized brain stem lesion identified by magnetic resonance imaging (MRI)].

E. Uyama, S. Araki, H. Kohrogi, 1988, Rinsho shinkeigaku = Clinical neurology.

[Clinical features of chronic Minamata disease (organic mercury poisoning). Analysis of the neurological findings in the most recent 100 cases].

M. Uchino, S. Araki, 1984, Rinsho shinkeigaku = Clinical neurology.

[A case of adult-onset tethered cord syndrome accompanied with slowly progressive muscular atrophy in the lower limbs].

S. Araki, T. Kumamoto, H. Ueyama, 1991, Rinsho shinkeigaku = Clinical neurology.

[Experimental chloroquine myopathy--morphological and biochemical studies].

S. Araki, T. Kumamoto, I. Toyoshima, 1984, Rinsho shinkeigaku = Clinical neurology.

[A case of ischemic disturbance of inner ear].

T. Nakagawa, Y. Hashimoto, S. Araki, 1989, Rinsho shinkeigaku = Clinical neurology.

Anticipation of age-of-onset in familial amyloidotic polyneuropathy and its pathogenesis.

S. Araki, 1995, Internal medicine.

Editorial Amyloid fibril protein

C. Masters, S. Ikeda, G. Merlini, 2002 .

Experimental neuropathy induced by methyl mercury compounds: autoradiographic study of GABA uptake by dorsal root ganglia.

K. Araki, T. Miyatake, S. Araki, 1986, European neurology.

[A case of cerebral thrombosis presenting global aphasia without hemiparesis].

H. Makino, Y. Hashimoto, S. Araki, 1990, Rinsho shinkeigaku = Clinical neurology.

A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy.

S. Tanase, S. Araki, T. Kumamoto, 1992, Biochemical and biophysical research communications.