MYOPATHY DUE TO GLYCOGEN-STORAGE DISEASE - PATHOLOGICAL AND BIOCHEMICAL-STUDIES IN RELATION TO GLYCOGENOSOME FORMATION

被引：25
|
作者：
IWAMASA, T
FUKUDA, S
TOKUMITSU, S
NINOMIYA, N
MATSUDA, I
OSAME, M
机构：
[1] KUMAMOTO UNIV, SCH MED, DEPT PEDIAT, KUMAMOTO 860, JAPAN
[2] KAGOSHIMA UNIV, SCH MED, DEPT BUNKYO KU, KAGOSHIMA 890, JAPAN
来源：
EXPERIMENTAL AND MOLECULAR PATHOLOGY | 1983年 / 38卷 / 03期
关键词：
D O I：
10.1016/0014-4800(83)90080-1
中图分类号：
R36 [病理学];
学科分类号：
100104 ;
摘要：
引用
收藏
页码：405 / 420
页数：16
相关论文
共 50 条
  • [41] NIEMANN-PICK DISEASE, TYPE-A - PATHOLOGICAL, HISTOCHEMICAL, ULTRASTRUCTURAL AND BIOCHEMICAL-STUDIES IN AN INFANT AND A FETUS
    FUKUDA, M
    TANAKA, A
    IWAMURA, C
    ISSHIKI, G
    NAKAMURA, S
    HASE, Y
    KOBAYASHI, Y
    MATSUMOTO, M
    KITAGAWA, Y
    MORIHANA, Y
    BRAIN & DEVELOPMENT, 1984, 6 (02): : 232 - 232
  • [42] CELL-CULTURE STUDIES ON CLASSIC AND VARIANT FORMS OF TYPE-II GLYCOGEN-STORAGE DISEASE (GSD)
    SHANSKE, S
    SHANSKE, A
    NITOWSKY, HM
    PEDIATRIC RESEARCH, 1974, 8 (04) : 395 - 395
  • [43] ADULT-ONSET LYSOSOMAL STORAGE DISEASE IN A SCHIPPERKE DOG - CLINICAL, MORPHOLOGICAL AND BIOCHEMICAL-STUDIES
    KNOWLES, K
    ALROY, J
    CASTAGNARO, M
    RAGHAVAN, SS
    JAKOWSKI, RM
    FREDEN, GO
    ACTA NEUROPATHOLOGICA, 1993, 86 (03) : 306 - 312
  • [44] Glycogen storage disease type 1a in Israel: Biochemical, clinical, and mutational studies
    Parvari, R
    Lei, KJ
    Bashan, N
    Hershkovitz, E
    Korman, SH
    Barash, V
    LermanSagie, T
    Mandel, H
    Chou, JY
    Moses, SW
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 72 (03): : 286 - 290
  • [45] CANINE GLYCOGEN-STORAGE DISEASE TYPE-II - A BIOCHEMICAL-STUDY OF AN ACID ALPHA-GLUCOSIDASE-DEFICIENT LAPLAND DOG
    WALVOORT, HC
    SLEE, RG
    KOSTER, JF
    BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 715 (01) : 63 - 69
  • [46] BIOCHEMICAL GENETICS OF THE LAPLAND DOG-MODEL OF GLYCOGEN-STORAGE DISEASE TYPE-II (ACID ALPHA-GLUCOSIDASE DEFICIENCY)
    WALVOORT, HC
    SLEE, RG
    SLUIS, KJ
    KOSTER, JF
    REUSER, AJJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (03): : 589 - 598
  • [47] NEW FAMILIAL VISCERAL MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA - CLINICAL, PATHOLOGICAL AND BIOCHEMICAL-STUDIES OF CONTRACTILE PROTEINS IN FRESH AND CULTURED STOMACH MUSCLE-CELLS
    IONASESCU, V
    ANURAS, S
    CHRISTENSEN, J
    IONASESCU, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 1981, 33 (06) : A80 - A80
  • [48] GLYCOGENOSIS TYPE-II - POMPES DISEASE - REPORT OF 2 SIBLINGS WITH HYPERTROPHIC SUB-AORTIC-STENOSIS DUE TO GLYCOGEN-STORAGE
    LEITRITZ, H
    APITZ, J
    KEMTER, B
    LOSER, H
    SCHMALTZ, AA
    MONATSSCHRIFT KINDERHEILKUNDE, 1973, 121 (09) : 584 - 589
  • [49] STUDIES OF THE RESIDUAL GLYCOGEN BRANCHING ENZYME-ACTIVITY PRESENT IN HUMAN-SKIN FIBROBLASTS FROM PATIENTS WITH TYPE-IV GLYCOGEN-STORAGE DISEASE
    BROWN, DH
    BROWN, BI
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 111 (02) : 636 - 643
  • [50] DEFICIENT GLUCOSE PHOSPHORYLATION AS A POSSIBLE COMMON DENOMINATOR AND ITS RELATION TO ABNORMAL LEUKOCYTE FUNCTION, IN GLYCOGEN-STORAGE DISEASE-1B PATIENTS
    BASHAN, N
    POTASHNIK, R
    PEIST, A
    PELEG, N
    MORAN, A
    MOSES, SW
    EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 : S44 - S48
12345