116 results on '"Suehara M"'
Search Results
2. CBCT-based Diagnosis of Periapical Lesion of Maxillary First Premolar Mimicking That of Second Premolar
3. Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X-linked Charcot–Marie–Tooth disease
4. HLA class I and class II of the Nivkhi, an indigenous population carrying HTLV-I in Sakhalin, Far Eastern Russia
5. Microscopic Endodontics in Infected Root Canal with Calcified Structure: A Case Report
6. Clinical course of hereditary motor and sensory neuropathy, Okinawa type
7. Laser welding method for removal of instruments debris from root canals
8. Germanium myopathy: clinical and experimental pathological studies
9. Actin stabilization induces apoptosis in cultured porcine epithelial cell rests of Malassez
10. Actin stabilization induces apoptosis in cultured porcine epithelial cell rests of Malassez.
11. Hypoxia Induces Expression and Activation of AMPK in Rat Dental Pulp Cells
12. Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant Connexin 32 (GJB1)
13. Action of synthetic tetragastrin on gastric secretion in man, especially in the cases of chronic gastritis
14. Statistical studies of peptic ulcers by sex, age, and operative indication
15. INFLAMMATORY CHANGES IN HAM/TSP OCCUR SIMULTANEOUSLY IN THE ENTIRE CNS: HISTOPATHOLOGIC ANALYSIS OF FOUR AUTOPSY CASES
16. A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths
17. Frameshift mutation in the collagen VI gene causes Ullrich's disease.
18. Lambert-Eaton myasthenic syndrome with ophthalmoparesis and pseudoblepharospasm.
19. Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene
20. A novel MPZgene mutation in dominantly inherited neuropathy with focally folded myelin sheaths
21. Localized scleroderma associated with progressing ischemic stroke
22. Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1
23. Germline mosaicism of MPZ Gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis
24. Acute disseminated myelitis after Japanese B encephalitis vaccination
25. Immunological abnormality in patients with lysinuric protein intolerance
26. A case of rigid spine syndrome associated with severe respiratory failure
27. Mitochondrial encephalomyopathy with no opthalmoplegia
28. Electroencephalographic Abnormalities in Human T-Cell Lymphotropic Virus Type I-Associated Myelopathy
29. High CSF lactate and pyruvate content in Kearns-Sayre syndrome
30. Successful development of novel monoclonal antibodies against HTLV-1 bZIP factor and their applications in studying the pathogenesis of HAM/TSP
31. Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications.
32. Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
33. The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients.
34. [Clinical manifestations of 5 patients with idiopathic paroxysmal kinesigenic choreoathetosis].
35. Three-tesla magnetic resonance neurography of the brachial plexus in cervical radiculopathy.
36. An endodontic-periodontal lesion with primary periodontal disease: a case report on its bacterial profile.
37. Persistent hiccups and vomiting with multiple cranial nerve palsy in a case of zoster sine herpete.
38. Digital video image processing from dental operating microscope in endodontic treatment.
39. [Autopsy case of a patient with Charcot-Marie-Tooth disease type 1A and suspected chronic inflammatory demyelinating polyradiculoneuropathy, which was later diagnosed as amyotrophic lateral sclerosis].
40. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.
41. In situ measurements of the dynamics of single giant DNA molecules at the toluene-trioctylamine/water interface by total internal reflection fluorescence microscopy.
42. High magnification microscopic system focusing on transparent liquid/liquid interface formed in thin-layer two-phase microcell.
43. Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.
44. Evaluation of wear and subsequent dye penetration of endodontic temporary restorative materials.
45. Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency.
46. Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency.
47. Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency.
48. Miyoshi myopathy patients with novel 5' splicing donor site mutations showed different dysferlin immunostaining at the sarcolemma.
49. Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease.
50. Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease.
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