195 results on '"Goto, Ikuo"'
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152. Vibrio parahaemolyticus Infectious Disease Cased by Kanagawa Phenomenon-Negative O3: K6 Originated from Maldives
153. Polymorphisms of apolipoprotein C-III in two cases with sialidase deficiency
154. Serum acetylcholine receptor antibody measurement in myasthenia gravis
155. A quantitative study of the muscle satellite cells in various neuromuscular disorders
156. Fabry's disease with partially deficient hydrolysis of ceramide trihexoside
157. Vacuoles in lymphocytes in adult type mucolipidosis
158. Adrenoleukodystrophy and variants
159. Expression of HTLV-I antigen in cultured peripheral blood mononuclear cells from patients with HTLV-I associated myelopathy
160. Leukoencephalopathy in HTLV-I-associated myelopathy: MRI and EEG data
161. Hydrolysis of galactosylsphingosine and lactosylsphingosine by β-galactosidases in human brain and cultured fibroblasts
162. 寄書
163. Effects of methylcobalamin on vitamin B1- and B-deficient encephalopathy in rats
164. The twitcher mouse: attenuated processes of Schwann cells in unmyelinated fibers
165. A simple diagnostic method of adrenoleukodystrophy: total fatty acid analysis of erythrocyte membranes
166. Second Interim Report of the Nation-Wide Collaborative Study on the Long-Term Effects of Bromocriptine in the Treatment of Parkinsonian Patients
167. Plasmalogen deficiency in cultured skin fibroblasts from neonatal adrenoleukodystrophy
168. Serial in vivo determination of motor conduction velocity in tails of alloxanized non-diabetic and diabetic rats
169. “Myopathic” changes in chorea-acanthocytosis
170. Beriberi neuropathy
171. Metabolism of free sphingoid bases in murine tissues and in cultured human fibroblasts
172. Proteolytic enzyme activities in mononuclear cells and granulocytes of patients with various neurological disorders
173. The rigid spine syndrome and Emery-Dreifuss muscular dystrophy
174. Tightly bound fatty acids in the erythrocyte membrane proteins in myotonic dystrophy
175. Leukocyte Protease Activities in Myotonic Dystrophy: Studies on Effects of Protease Inhibitors
176. Structure and expression of the alternatively-spliced forms of mRNA for the mouse homolog of Alzheimer's disease amyloid beta protein precursor
177. An Epidemiological Study of Serratia marcescens Infections by Bacteriocin Typing
178. Thiamine-deficient encephalopathy in rats: Effects of deficiencies of thiamine and magnesium
179. Accumulation of lysosulfatide (sulfogalactosylsphingosine) in tissues of a boy with metachromatic leukodystrophy
180. A comparison of erythrocytes, lymphocytes and blood plasma as samples in fatty acid analysis for the diagnosis of adrenoleukodystrophy
181. Systemic triglyceride storage disease with normal carnitine: a putative defect in long-chain fatty acid metabolism
182. Generation of CD4+ blastoid T cells showing marked upregulation of CD4, class I and II MHC, and IL2 receptor molecules is required for the expression of potent encephalitogenicity
183. The twitcher mouse: accumulation of galactosylsphingosine and pathology of the sciatic nerve
184. Incidence of Intestinal Protozoal Infection in Traveller's Diarrhoea
185. CASE OF NEUROFIBROMATOSIS WITH ADRENAL PHEOCHROMOCYTOMA AND CEREBRAL ASTROCYTOMA. CASE REPORT
186. Serial in vivo determinations of nerve conduction velocity in rat tails. Physiological and pathological changes
187. LOWERING OF BLOOD-PRESSURE BY HYPERVENTILATION IN PRIMARY ALDOSTERONISM
188. Familial occurrence of multiple intracranial aneurysms
189. Creatine Phosphokinase
190. Adrenoleukodystrophy
191. Nonfamilial Prealbumin-Type Amyloid Polyneuropathy
192. Effects of methylcobalamin on vitamin B 1- and B-deficient encephalopathy in rats
193. Beriberi neuropathy: Morphometric study of sural nerve
194. Antibody titers to HTLV-I-p40 tax protein and gag-env hybrid protein in HTLV-I-associated myelopathy/tropical spastic paraparesis: Correlation with increased HTLV-I proviral DNA load
195. Serum creatine phosphokinase isozymes in hypothyroidism, convulsion, myocardial infarction and other diseases
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