進行性遺伝性腎炎の臨床病理学的検討:糸球体基底膜病変の電顕観察を中心に
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Published in | 日本腎臓学会誌 Vol. 34; no. 11; pp. 1135 - 1148 |
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Main Author | |
Format | Journal Article |
Language | Japanese |
Published |
社団法人 日本腎臓学会
25.11.1992
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Online Access | Get full text |
ISSN | 0385-2385 1884-0728 |
DOI | 10.14842/jpnjnephrol1959.34.1135 |
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Author | 吉田, 礼子 |
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References | 22) Duffy JL, Cinque T, Grishman E, Churg J: Intraglomerular fibrin, platelet aggregation and subendothelial deposits in lipoid nephrosis. J Clin Invest 49: 251-258, 1970 21) 山辺英彰:ネフローゼ症候群,慢性糸球体腎炎などにおける血液の凝固線溶系について,日腎誌21:219-230,1979 17) 甲田豊:糸球体の巣状硬化病変形成過程の電子顕微鏡的観察,日腎誌30:313-329,1988 12) Morita M, Sakaguchi: A quontitative study of glomerular basement membrane changes in IgA nephropathy. J pathol 154: 7-18, 1988 20) Kihara I, Yaoita E, Yamamoto T: Cellular processes of glomerular adhesion in aged rats. Acta Medica et Biologica 38(Suppl.): 69-80, 1990 8) Habib R. Gubler M-C, Hinglais N, Noel L-H, Droz D, Levy M, Mahieu P, Foidart J-M, Perrin D, Bois E, Grünfeld J-P: Alport's syndrome: Experience at hôpital Necker. Kidney Int 21 (supple 11): 20-28, 1982 23) 水野愛子,児玉真澄,矢崎雄彦,新家雪彦:ネフローゼ症候群を呈するアルポート症候群児への薬物治療,小児科臨床44:243-247,1991 14) Basta-Jovanovic G, Venkataseshan VS, Churg J Correlation of glomerular basement membrane alterations with clinical data in progressive hereditary nephritis (Alport's syndrome). Am J Kidney Diseases 16: 51-56, 1990 2) Hinglais N, Grunfeld J-P, Bois E: Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome). Laboratory Investigation 27: 473-487, 1972 19) Remuzzi G, Bertani T: Is glomerulosclerosis a consequence of altered glomerular permeability to macromolecules? Kidney lnt 38: 384-394, 1990 4) Churg J, Sherman RL: Pathologic characteristics of hereditary nephritis. Arch Pathol 95: 374-379, 1973 9) Shaw RF, Kallen RJ: Population genetics of Alport's syndrome. Nephron 16: 427-432, 1976 10) 武田修明,藤田篤史,田中陸男,和田博義:進行性遺伝性腎炎の臨床病理学的検討―アンケート調査を中心に―日児誌93:911-917 ,1989 11) Atkin CL, Gregory MC, Border WA: Alport syndrome, in Diseases of the Kidney, edited by Schrier RW, Gottschalk CW, Boston, Little Brown, 1988, pp 617-641 16) Morita T, Suzuki Y, Churg J: Structure and development of the glomerular crescent. Am J Pathol 72: 349-368, 1973 1) Grünfeld J-P: The clinical spectrum of hereditary nephritis. Kidney Int 27: 83-92, 1985 18) Rennke HG, Klein PS: Pathogenesis and significance of nonprimary focal and segmetal glomerulosclerosis. Am J Kidney Dis 13: 443-456, 1989 13) Rumpelt H-J: Hereditary nephropathy (Alport syndrome): correlation of clinical date with glome-rular basement membrane alterations. Clin Nephrol 13: 203-207, 1980 3) Spear GS, Slusser RJ: Alport's syndrome. Emphasizing electron microscopic studies of the Glomerulus. Am J Pathol 69: 213-220, 1972 6) Kohaut EC, Singer DB, Nevels BK, Hill LL: The specificity of split renal membranes in hereditary nephritis. Arch Pathol Lab Med 100: 475-479, 1976 7) Yoshikawa N, Cameron AH, White RHR: The glomerular basal lamina in hereditary nephritis. J Pathology 135: 199-209, 1981 15) 木原達,高田恒郎,柳原俊雄:アルポート症候群の進行要因:糸球体基底膜の断裂について,厚生省心身障害研究小児慢性腎疾患の予後,管理,治療に関する研究(主任研究者石丸隆治)昭和63年度研究報告,p26 5) Gaboardi F, Edefonti A, Imbasciati E, Tarantino A, Mihatsch MJ, Zollinger HU: Alport's syndrome (progressive hereditary nephritis). Clin Nephrol 2: 143-156, 1974 |
References_xml | – reference: 1) Grünfeld J-P: The clinical spectrum of hereditary nephritis. Kidney Int 27: 83-92, 1985 – reference: 15) 木原達,高田恒郎,柳原俊雄:アルポート症候群の進行要因:糸球体基底膜の断裂について,厚生省心身障害研究小児慢性腎疾患の予後,管理,治療に関する研究(主任研究者石丸隆治)昭和63年度研究報告,p26 – reference: 3) Spear GS, Slusser RJ: Alport's syndrome. Emphasizing electron microscopic studies of the Glomerulus. Am J Pathol 69: 213-220, 1972 – reference: 18) Rennke HG, Klein PS: Pathogenesis and significance of nonprimary focal and segmetal glomerulosclerosis. Am J Kidney Dis 13: 443-456, 1989 – reference: 20) Kihara I, Yaoita E, Yamamoto T: Cellular processes of glomerular adhesion in aged rats. Acta Medica et Biologica 38(Suppl.): 69-80, 1990 – reference: 12) Morita M, Sakaguchi: A quontitative study of glomerular basement membrane changes in IgA nephropathy. J pathol 154: 7-18, 1988 – reference: 16) Morita T, Suzuki Y, Churg J: Structure and development of the glomerular crescent. Am J Pathol 72: 349-368, 1973 – reference: 22) Duffy JL, Cinque T, Grishman E, Churg J: Intraglomerular fibrin, platelet aggregation and subendothelial deposits in lipoid nephrosis. J Clin Invest 49: 251-258, 1970 – reference: 10) 武田修明,藤田篤史,田中陸男,和田博義:進行性遺伝性腎炎の臨床病理学的検討―アンケート調査を中心に―日児誌93:911-917 ,1989 – reference: 11) Atkin CL, Gregory MC, Border WA: Alport syndrome, in Diseases of the Kidney, edited by Schrier RW, Gottschalk CW, Boston, Little Brown, 1988, pp 617-641 – reference: 17) 甲田豊:糸球体の巣状硬化病変形成過程の電子顕微鏡的観察,日腎誌30:313-329,1988 – reference: 23) 水野愛子,児玉真澄,矢崎雄彦,新家雪彦:ネフローゼ症候群を呈するアルポート症候群児への薬物治療,小児科臨床44:243-247,1991 – reference: 5) Gaboardi F, Edefonti A, Imbasciati E, Tarantino A, Mihatsch MJ, Zollinger HU: Alport's syndrome (progressive hereditary nephritis). Clin Nephrol 2: 143-156, 1974 – reference: 9) Shaw RF, Kallen RJ: Population genetics of Alport's syndrome. Nephron 16: 427-432, 1976 – reference: 8) Habib R. Gubler M-C, Hinglais N, Noel L-H, Droz D, Levy M, Mahieu P, Foidart J-M, Perrin D, Bois E, Grünfeld J-P: Alport's syndrome: Experience at hôpital Necker. Kidney Int 21 (supple 11): 20-28, 1982 – reference: 6) Kohaut EC, Singer DB, Nevels BK, Hill LL: The specificity of split renal membranes in hereditary nephritis. Arch Pathol Lab Med 100: 475-479, 1976 – reference: 4) Churg J, Sherman RL: Pathologic characteristics of hereditary nephritis. Arch Pathol 95: 374-379, 1973 – reference: 2) Hinglais N, Grunfeld J-P, Bois E: Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome). Laboratory Investigation 27: 473-487, 1972 – reference: 13) Rumpelt H-J: Hereditary nephropathy (Alport syndrome): correlation of clinical date with glome-rular basement membrane alterations. Clin Nephrol 13: 203-207, 1980 – reference: 19) Remuzzi G, Bertani T: Is glomerulosclerosis a consequence of altered glomerular permeability to macromolecules? Kidney lnt 38: 384-394, 1990 – reference: 7) Yoshikawa N, Cameron AH, White RHR: The glomerular basal lamina in hereditary nephritis. J Pathology 135: 199-209, 1981 – reference: 21) 山辺英彰:ネフローゼ症候群,慢性糸球体腎炎などにおける血液の凝固線溶系について,日腎誌21:219-230,1979 – reference: 14) Basta-Jovanovic G, Venkataseshan VS, Churg J Correlation of glomerular basement membrane alterations with clinical data in progressive hereditary nephritis (Alport's syndrome). Am J Kidney Diseases 16: 51-56, 1990 |
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Title | 進行性遺伝性腎炎の臨床病理学的検討:糸球体基底膜病変の電顕観察を中心に |
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