FAMILIAL OCULOLEPTOMENINGEAL AMYLOIDOSIS - REPORT OF A NEW FAMILY WITH UNUSUAL FEATURES

被引：52

作者：

UITTI, RJ

DONAT, JR

ROZDILSKY, B

SCHNEIDER, RJ

KOEPPEN, AH

机构：

[1] UNIV SASKATCHEWAN,DEPT CLIN NEUROL SCI,SASKATOON S7N 0W0,SASKATCHEWAN,CANADA

[2] UNIV SASKATCHEWAN,DEPT PATHOL,SASKATOON S7N 0W0,SASKATCHEWAN,CANADA

[3] UNIV SASKATCHEWAN,DEPT OPHTHALMOL,SASKATOON S7N 0W0,SASKATCHEWAN,CANADA

[4] VET ADM MED CTR,NEUROL SERV,ALBANY,NY 12208

来源：

ARCHIVES OF NEUROLOGY | 1988年 / 45卷 / 10期

关键词：

D O I：

10.1001/archneur.1988.00520340072015

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：1118 / 1122

页数：5

共 13 条

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[4] ABNORMAL-METABOLISM OF GAMMA-TRACE ALKALINE MICROPROTEIN - THE BASIC DEFECT IN HEREDITARY CEREBRAL-HEMORRHAGE WITH AMYLOIDOSIS
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[5] HEREDITARY CEREBRAL HEMORRHAGE WITH AMYLOIDOSIS
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[J]. BRAIN, 1972, 95 : 387 - +
[6] UNUSUAL CAUSE OF VITREOUS OPACITIES - PRIMARY FAMILIAL AMYLOIDOSIS
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[J]. OPHTHALMOLOGICA, 1971, 162 (03) : 173 - &
[7] TRANSTHYRETIN - A CHOROID PLEXUS-SPECIFIC TRANSPORT PROTEIN IN HUMAN-BRAIN
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[J]. NEUROLOGY, 1986, 36 (07) : 900 - 911
[8] PORTUGUESE TYPE OF FAMILIAL AMYLOID POLYNEUROPATHY - ANATOMOCLINICAL STUDY OF A BRAZILIAN FAMILY
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[J]. EUROPEAN NEUROLOGY, 1974, 11 (03) : 180 - 195
[9] FAMILIAL AMYLOID POLYNEUROPATHY
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[J]. MUSCLE & NERVE, 1985, 8 (09) : 733 - 749
[10] Mancini G, 1965, Immunochemistry, V2, P235, DOI 10.1016/0019-2791(65)90004-2

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