書籍詳細

―剖検例検討―

P.8 掲載の参考文献

• 1) Nakanishi T, et al:The Crow-Fukase syndrome:a study of 102 cases in Japan. Neurology 34:712, 1984.
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• 2) Dyck PJ, et al:Plasma exchange in polyneuropathy associated with monoclonal gammopathy of undetermined significance. N. Engl. J. Med. 21:1482, 1991.
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• 3) Grander D, et al:Influence of interferon on antibody production and viability of malignant cells from patients with multiple myeloma. Eur. J. Haematol. 46:17, 1991.
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• 4) Durie BGM, et al:Pretreatment tumor mass, cell kinetics and prognosis in multiple myeloma. Blood 55:364, 1980.

• 5) Berkman SA, et al:Clinical uses of intravenous immunoglobulins. Ann. Int. Med. 112:278, 1990.
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P.14 掲載の参考文献

• 1) Linsenmayer TF:Collagen. Cell biology of extracellular matrix (ed by Hay ED), Plenum, New York, 1991, pp. 7-44.

• 2) Chu M-L, Williams CJ, Pepe G, et al:Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta. Nature 304:78-80, 1983.

• 3) Kuivaniemi H, Tromp G and Prockop DJ:Mutations in collagen genes;causes of rare and some common diseases in humans. FASEB J. 5:2052-2060, 1991.
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• 4) McKusick VA:Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes, sixth ed. The Johns Hopkins University Press, Baltimore, 1983.

• 5) Weil D, Bernard M, Combates N, et al:Identification of a mutation that causes exon skipping during collagen pre-mRNA splicing in an Ehlers-Danlos syndrome variant. J. Biol. Chem. 263:8561-8564, 1988.

• 6) Cole WG, Chiodo AA, Lamande SR, et al:A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV. J. Biol. Chem. 265:17070-17077, 1990.

• 7) Lee B, Vissing H, Ramirez F, et al:Identification of the molecular defect in a family with spondyloepiphyseal dysplasia. Science 244:978-980, 1989.

• 8) Vissing H, D'Alessio M, Lee B, et al:Glycine to serine substitution in the triple helical domain of proα1 (II) collagen results in a lethal perinatal form of short-limbed dwarfism. J. Biol. Chem. 264:18265-18267, 1989.

• 9) Ahmad NN, Ala-Kokko L, Knowlton RG, et al:A stop codon in the gene for type II procollagen (COL2A1) causes one variant of arthro-ophthalmopathy (the Stickler syndrome). Am. J. Hum. Genet. 47:A206, 1990.

• 10) Ala-Kokko L, Baldwin CT, Moskowitz RW, et al:Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia. Proc. Natl. Acad. Sci. USA 87:6565-6568, 1990.
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• 11) Bernard M, Yoshioka H, Rodriguez E, et al:Cloning and sequencing of pro-α1 (XI) collagen cDNA demonstrates that type XI belongs to the fibrillar class of collagens and reveals that the expression of the gene is not restricted to cartilagenous tissue. J. Biol. Chem. 263:17159-17166, 1988.

• 12) Kimura T, Mattei M-G, Stevens JW, et al:Molecular cloning of rat and human type IX collagen cDNA and localization of the α1 (IX) gene on the human chromosome 6. Eur. J. Biochem. 179:71-78, 1989.

• 13) Kimura T, Cheah KSE, Chan SDH, et al:The human α2 (XI) collagen (COL11A2) chain. J. Biol. Chem. 264:13910-13916, 1989.

• 14) Spotila L, Constantinou CD, Sereda L, et al:Substitution of serine for gly α2-661 in the gene for type I procollagen (COL1A2) as a cause of post-menopausal osteoporosis. Am. J. Hum. Genet. 47:A237, 1990.

• 15) Kontusaari S, Tromp G, Kuivaniemi H, et al:Inheritance of an RNA splicing mutation (G+1 IVS20) in the type III procollagen gene (COL3A1) in a family having aortic aneurysms and easy bruisability:Phenotypic overlap between familial arterial aneurysms and Ehlers-Danlos syndrome type IV. Am. J. Hum. Genet. 47:112-120, 1990.

• 16) Nakata K, Ono K, Miyazaki J, et al:Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing α1 (IX) collagen chains with a central deletion. Proc. Natl. Acad. Sci. USA 90:2870-2874, 1993.

―発言1―

P.23 掲載の参考文献

• 1) Kyle RA, Bayrd ED:Amyloidosis:Review of 236 cases. Medicine 54:271-299, 1975.
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• 2) Linke RP:Monoclonal antibodies against fibril protein AA. Production, specificity, and use for immunohistochemical localization and classification of AA-type amyloidosis. J. Histochem. Cytochem. 32:322-328, 1984.
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• 3) Cohen AS, Connors LH:The pathogenesis and biochemistry of amyloidosis. J. Pathol. 151:1-10, 1987.
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• 4) 鳥山 一, 助川 淳, 東郷順子, 宮本二郎, 中原 朗, 囲廻道夫, 川北 勲, 小山捷平, 山形 袖, 武藤 弘, 三田村圭二, 福冨久之, 大菅俊明, 嶋田隆夫:胃内視鏡生検にてアミロイドーシスと診断された一例. Prog. Dig. Endosc. 17:236-239, 1980.

• 5) 有田 毅, 古沢 毅, 工藤輝俊, 坂本賢二郎, 江本 修, 柴田興彦:胃生検が確定診断の糸口になった原発性全身性アミロイドーシスの一例. 胃と腸 15:1227-1233, 1980.

• 6) 田口久雄, 荻野隆章, 一瀬忠邦, 棟久龍夫:胃生検で診断した続発性アミロイドーシスの一例. Gastroenterol. Endosc. 25:1523-1527, 1983.

• 7) 小出 章, 松本好市, 北川達士:胃の潰瘍性病変を契機として診断し得た全身性原発性アミロイドーシスの一例. Gastroenterol. Endosc. 34:1056-1059, 1992.

P.28 掲載の参考文献

• 1) 大田 寛, 七川歓次, 前田 晃・他:慢性関節リウマチの死因調査(315死亡例). 大阪府特定疾患研究会, 骨関節難病委員会調査研究結果報告書, 骨3-22, 平成4年3月.

• 2) 桜井幹己:慢性関節リウマチ剖検例にみる心アミロイドージスに関する組織病理学的検討. 大阪府特定疾患研究会, 骨関節難病委員会調査研究結果報告書, 骨1-2, 平成2年3月.

• 3) 新丸昭子, 林満寿彦, 前田 晃・他:慢性関節リウマチに合併したアミロイドージス12例についての臨床並びに病理学的検討. 臨床リウマチ 3:207-212, 1991.

• 4) Laasko M, Mutru OK, Isomaki H, et al:Mortality from amyloidosis and renal diseases in patients with rheumatoid arthritis. Ann. Rheum. Dis. 45:663-667, 1986.

• 5) Vandenbroucke JP, Hagevout HM and Cast A:Survival and cause of death in rheumatoid arthritis. J. Rheumatol. 11:158-161, 1984.

• 6) Missen GAK and Taylor JD:Amyloidosis in rheumatoid arthritis. J. Pathol. Bacteriol. 71:179-192, 1956.

• 7) Mutru OK, Koota K and Isomaki H:Cause of death in rheumatoid arthritis. Scand. J. Rheumatol. 5:239-240, 1976.

―発言2―

P.36 掲載の参考文献

• 1) Schnur PH:Clinical features of SLE. In Textbook of Rheumatology (eds by Kelly WN, et al), 3rd ed, WB Saunders Co., Philadelphia, 1989, p. 1101.

• 2) Osler W:On the visceral complications of erythema exudatium multiforme. Am. J. Med. Sci. 110:629-646, 1895.

• 3) Johnson JF:Systemic lupus erythematosus with abdominal crisis:An interesting and unusual case. J. Tenn. Med. Assoc. 79:13-14, 1986.

• 4) 建部高明:急性膵炎の病因と病態. 日内会誌 81:1901-1905, 1992.

• 5) 石原克哉, 温田信夫, 成田 真・他:肝内血腫を併発したSLEの1例. 日消病会誌 81:2668, 1984.

• 6) 谷口 誠, 山門 実, 安田 宏・他:特発性腎被膜下血腫を合併した全身性エリテマトーデスの1例. 日腎会誌, 30:1432, 1988.

• 7) Kagawa H, Okubo S and Yasunaga K:Plasma coagulation and fibrinolysis parameters in patients with collagen diseases, and analysis of the multimeric structure of von Willebrand factor (vWF). Int. J. Hematol. 54:429-439, 1991.
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―発言3―

P.46 掲載の参考文献

• 1) 七川歓次, 根来 茂/監修:第一回 (1990) 近畿リウマチ病研究会講演集. 癌と化学療法社, 東京, 1991.

• 2) Okabayashi A and Kondo Y (eds):Masugi nephritis and its immunopathologic implications. Igaku-Shoin, Tokyo, 1980.

• 3) 岡林 篤:実験的血管炎, 遷延感作ウサギにおけるThrombotic Microangiopathyの発生を中心に. 医学のあゆみ 37 (5):196-200, 1961.

• 4) 江頭靖之:家兎における連鎖球菌による副鼻腔感染に基づくリウマチ型あるいは結節性動脈周囲炎症型肺臓炎の実験. 日新医学 37:510-517, 1950.

• 5) 椎名岩松:ウサギにおける一側腎動脈結紮法を用いた反復馬杉腎炎の組織病理学的研究. 千葉医会誌 35:739-755, 1959.

• 6) 明石茂雄:慢性遷延感作ウサギに発生した類澱粉症の組織病理学的研究. 阪市大医誌 5:401-410, 1956.

• 7) 北条憲二:遷延感作と血清蛋白の変動, 実験的研究. アレルギー 10:554-564. 1961.

• 8) 矢崎光保・他:実験遷延感作における脳の病変. 旭中央医報 11:25-33. 1989.

• 9) 岡林 篤:結合組織病と免疫過程. 結合組織病 (大島良雄, 大高裕一・編). p. 297-313. 医学書院, 東京, 1969.

―特別講演―

P.60 掲載の参考文献

• 1) Horiuchi A, et al:Function of thymic reticuloepithelial cells in New Zealand mice. Acta Med. Kinki Univ. 4:345, 1979.

• 2) Minoda M and Horiuchi A:Function of thymic reticuloepithelial cells in mice. Thymic reticuloepithelial cells and T cell differentiation. Acta Haematol. Jap. 48:992, 1985.

• 3) Minoda M and Horiuchi A:The function of thymic reticuloepithelial cells in New Zealand mice. Thymus 5:363, 1983
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• 4) Minoda M and Horiuchi A:The effects of macrophages on interleukin 2 production in thymocytes of New Zealand black mice. J. Clin. Lab. Immunol. 22:29, 1987.
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• 5) Minoda M, Senda S and Horiuchi A:The relationship between the defect in the syngeneic mixed lymphocyte reaction and thymic abnormality in New Zealand mice. J. Clin. Lab. Immunol. 23:101, 1987.
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• 6) Minoda M, Funauchi M and Horiuchi A:Effect of interferon-γ on the abnormality of T cell activation in NZB mice. Clin. Immunol. Immunopathol. 49:283, 1988.

• 7) Minoda M, et al:Examination of the inhibitory effects of interferon-γ on interleukin-4-induced stimulation of resting B cells from NZB/NZW F1 mice. Clin. Exp. Immunol. 78:115, 1989.

• 8) 船内正憲, 蓑田正豪, 堀内 篤:膠原病患者におけるInterleukin-4, Interferon-γ 量とB細胞異常との関連. リウマチ 31:493, 1991.

• 9) 池田桂三:全身性エリテマトーデス患者血清中の抗DNA抗体に対する抗イディオタイプ抗体活性. 日臨免疫会誌 12:97, 1990.

• 10) 杉島 仁, 蓑田正豪:SLEモデルマウス脾細胞の抗DNA抗体産生に及ぼす抗イディオタイプ抗体の影響. アレルギー 40:711, 1991.
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• 11) 木下浩二:抗DNA抗体遣伝子の突然変異. クラス転換と抗原親和性の変化. 近畿大医誌 16:541, 1991.