HYPERURICEMIA AND NEUROLOGIC DEFICITS - A FAMILY STUDY

被引：41
作者：
ROSENBERG, AL
BERGSTROM, L
TROOST, BT
BARTHOLOMEW, BA
机构：
来源：
NEW ENGLAND JOURNAL OF MEDICINE | 1970年 / 282卷 / 18期
关键词：
D O I：
10.1056/NEJM197004302821802
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：992 / +
页数：1
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共 28 条
[1]   Hereditary familial congenital haemorrhagic nephritis. [J].
Alport, AC .
BMJ-BRITISH MEDICAL JOURNAL, 1927, 1927 :504-506
[2]   MALFORMATION OF THE ERYTHROCYTES IN A CASE OF ATYPICAL RETINITIS PIGMENTOSA [J].
BASSEN, FA ;
KORNZWEIG, AL .
BLOOD, 1950, 5 (04) :381-387
[3]  
Brown S., 1892, BRAIN, V15, P250
[4]  
ENGEL WK, 1966, MUSCLE BIOPSY CLINIC, P90
[5]   HEREDITARY RENAL DISEASE WITH NEUROSENSORY HEARING LOSS PROLINURIA AND ICHTHYOSIS [J].
GOYER, RA ;
REYNOLDS, J ;
BURKE, J ;
BURKHOLDER, P .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1968, 256 (03) :166-+
[6]  
GREENFIELD JG, 1954, SPINO CEREBELLAR DEG, P64
[7]   Familial cortical cerebellar atrophy [J].
Hall, B ;
Noad, KB ;
Latham, O .
BRAIN, 1941, 64 :178-U24
[8]   HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS DEAFNESS NEPHROPATHY + CEREBRAL DYSFUNCTION [J].
HERRMANN, C ;
AGUILAR, MJ ;
SACKS, OW .
NEUROLOGY, 1964, 14 (03) :212-+
[9]  
Holmes G, 1907, BRAIN, V30, P466
[10]   HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY IN GOUT [J].
KELLEY, WN ;
GREENE, ML ;
ROSENBLOOM, FM ;
HENDERSON, JF ;
SEEGMILLER, JE .
ANNALS OF INTERNAL MEDICINE, 1969, 70 (01) :155-+
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