INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS

被引:2
作者
SANTAVUORI, P
HALTIA, M
RAPOLA, J
RAITTA, C
KERANEN, A
机构
[1] UNIV HELSINKI,CHILDRENS HOSP,HELSINKI,FINLAND
[2] UNIV HELSINKI,EYE HOSP,HELSINKI,FINLAND
来源
ACTA GENETICAE MEDICAE ET GEMELLOLOGIAE | 1974年 / 23卷
关键词
D O I
10.1017/S1120962300023763
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:197 / 200
页数:4
相关论文
共 13 条
  • [1] COPENHAVER RM, 1960, ARCH OPHTHALMOL-CHIC, V63, P559
  • [2] LATE INFANTILE PROGRESSIVE ENCEPHALOPATHY WITH DISTURBED POLYUNSATURATED FAT METABOLISM
    HAGBERG, B
    SOURANDER, P
    SVENNERHOLM, L
    [J]. ACTA PAEDIATRICA SCANDINAVICA, 1968, 57 (06): : 495 - +
  • [3] INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS .2. MORPHOLOGICAL AND BIOCHEMICAL STUDIES
    HALTIA, M
    RAPOLA, J
    SANTAVUORI, P
    KERANEN, A
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (03) : 269 - 285
  • [4] Menkes J H, 1971, J Pediatr, V79, P183, DOI 10.1016/S0022-3476(71)80100-2
  • [5] NEUROPHYSIOLOGICAL IDENTIFICATION OF A LATE INFANTILE FORM OF NEURONAL LIPIDOSIS
    PAMPIGLIONE, G
    HARDEN, A
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1973, 36 (01) : 68 - 74
  • [6] PLUM CM, 1961, ACTA NEUROL SCAND, V37, P243
  • [7] RAITTA C, 1973, ACT GENET M, V23, P193
  • [8] RAYNER S, 1962, HEREDITAS LUND, P107
  • [9] INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS .1. CLINICAL STUDY OF 15 PATIENTS
    SANTAVUORI, P
    HALTIA, M
    RAPOLA, J
    RAITTA, C
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (03) : 257 - 267
  • [10] SVENNERHOLM L, IN PRESS