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THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - AN EXPERIMENT OF NATURE IN GLYCOSYLATION
被引:19
作者
:
WINCHESTER, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
WINCHESTER, B
CLAYTON, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
CLAYTON, P
MIAN, N
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
MIAN, N
DITOMASO, E
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
DITOMASO, E
DELL, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
DELL, A
REASON, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
REASON, A
KEIR, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
KEIR, G
机构
:
[1]
UNIV LONDON,NEUROL INST,DEPT CLIN NEUROCHEM,LONDON,ENGLAND
[2]
UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED,DEPT BIOCHEM,LONDON SW7 2AS,ENGLAND
来源
:
BIOCHEMICAL SOCIETY TRANSACTIONS
|
1995年
/ 23卷
/ 01期
关键词
:
D O I
:
10.1042/bst0230185
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
引用
收藏
页码:185 / 188
页数:4
相关论文
共 15 条
[1]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - NORMAL GLYCOSYLATION IN THE FETUS
[J].
CLAYTON, P
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
CLAYTON, P
;
WINCHESTER, B
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
WINCHESTER, B
;
DITOMASO, E
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
DITOMASO, E
;
YOUNG, E
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
YOUNG, E
;
KEIR, G
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
KEIR, G
;
RODECK, C
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
RODECK, C
.
LANCET,
1993,
341
(8850)
:956
-956
[2]
FAMILIAL OLIVOPONTOCEREBELLAR ATROPHY WITH NEONATAL ONSET - A RECESSIVELY INHERITED SYNDROME WITH SYSTEMIC AND BIOCHEMICAL-ABNORMALITIES
[J].
HARDING, BN
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
HARDING, BN
;
DUNGER, DB
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
DUNGER, DB
;
GRANT, DB
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
GRANT, DB
;
ERDOHAZI, M
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
ERDOHAZI, M
.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
1988,
51
(03)
:385
-390
[3]
OLIVOPONTOCEREBELLAR ATROPHY OF NEONATAL ONSET AND DISIALOTRANSFERRIN DEVELOPMENT DEFICIENCY SYNDROME
[J].
HORSLEN, SP
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HORSLEN, SP
;
CLAYTON, PT
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
CLAYTON, PT
;
HARDING, BN
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HARDING, BN
;
HALL, NA
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HALL, NA
;
KEIR, G
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
KEIR, G
;
WINCHESTER, B
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
WINCHESTER, B
.
ARCHIVES OF DISEASE IN CHILDHOOD,
1991,
66
(09)
:1027
-1032
[4]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN-SYNDROME TYPE-II - A DEFICIENCY IN GOLGI LOCALIZED N-ACETYL-GLUCOSAMINYLTRANSFERASE-II
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
JAEKEN, J
;
SCHACHTER, H
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
SCHACHTER, H
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
CARCHON, H
;
DECOCK, P
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
DECOCK, P
;
CODDEVILLE, B
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
CODDEVILLE, B
;
SPIK, G
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
SPIK, G
.
ARCHIVES OF DISEASE IN CHILDHOOD,
1994,
71
(02)
:123
-127
[5]
THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - PRE-GOLGI AND GOLGI DISORDERS
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
JAEKEN, J
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
CARCHON, H
;
STIBLER, H
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
STIBLER, H
.
GLYCOBIOLOGY,
1993,
3
(05)
:423
-428
[6]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-II
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
JAEKEN, J
;
DECOCK, P
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
DECOCK, P
;
STIBLER, H
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
STIBLER, H
;
VANGEET, C
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
VANGEET, C
;
KINT, J
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
KINT, J
;
RAMAEKERS, V
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
RAMAEKERS, V
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
CARCHON, H
.
JOURNAL OF INHERITED METABOLIC DISEASE,
1993,
16
(06)
:1041
-1041
[7]
THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - AN OVERVIEW
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
Centre for Metabolic Diseases, Department of Pediatrics, University of Leuven
JAEKEN, J
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
Centre for Metabolic Diseases, Department of Pediatrics, University of Leuven
CARCHON, H
.
JOURNAL OF INHERITED METABOLIC DISEASE,
1993,
16
(05)
:813
-820
[8]
SERUM LYSOSOMAL-ENZYME ABNORMALITIES IN GALACTOSEMIA
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
STATE UNIV GHENT,DEPT PAEDIAT,B-9000 GENT,BELGIUM
JAEKEN, J
;
KINT, J
论文数:
0
引用数:
0
h-index:
0
机构:
STATE UNIV GHENT,DEPT PAEDIAT,B-9000 GENT,BELGIUM
KINT, J
;
SPAAPEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
STATE UNIV GHENT,DEPT PAEDIAT,B-9000 GENT,BELGIUM
SPAAPEN, L
.
LANCET,
1992,
340
(8833)
:1472
-1473
[9]
DISIALOTRANSFERRIN DEVELOPMENTAL DEFICIENCY SYNDROME AND OLIVOPONTOCEREBELLAR ATROPHY
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LEUVEN,BELGIUM
UNIV HOSP GASTHUISBERG,DEPT PAEDIAT,B-3000 LEUVEN,BELGIUM
JAEKEN, J
.
ARCHIVES OF DISEASE IN CHILDHOOD,
1989,
64
(05)
:764
-765
[10]
JAEKEN J, 1989, GENETICS NEUROPSYCHI, P69
←
1
2
→
共 15 条
[1]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - NORMAL GLYCOSYLATION IN THE FETUS
[J].
CLAYTON, P
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
CLAYTON, P
;
WINCHESTER, B
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
WINCHESTER, B
;
DITOMASO, E
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
DITOMASO, E
;
YOUNG, E
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
YOUNG, E
;
KEIR, G
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
KEIR, G
;
RODECK, C
论文数:
0
引用数:
0
h-index:
0
机构:
INST NEUROL,DEPT CLIN NEUROCHEM,LONDON WC1,ENGLAND
RODECK, C
.
LANCET,
1993,
341
(8850)
:956
-956
[2]
FAMILIAL OLIVOPONTOCEREBELLAR ATROPHY WITH NEONATAL ONSET - A RECESSIVELY INHERITED SYNDROME WITH SYSTEMIC AND BIOCHEMICAL-ABNORMALITIES
[J].
HARDING, BN
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
HARDING, BN
;
DUNGER, DB
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
DUNGER, DB
;
GRANT, DB
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
GRANT, DB
;
ERDOHAZI, M
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,INST CHILD HLTH,LONDON WC1N 3JH,ENGLAND
ERDOHAZI, M
.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY,
1988,
51
(03)
:385
-390
[3]
OLIVOPONTOCEREBELLAR ATROPHY OF NEONATAL ONSET AND DISIALOTRANSFERRIN DEVELOPMENT DEFICIENCY SYNDROME
[J].
HORSLEN, SP
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HORSLEN, SP
;
CLAYTON, PT
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
CLAYTON, PT
;
HARDING, BN
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HARDING, BN
;
HALL, NA
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
HALL, NA
;
KEIR, G
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
KEIR, G
;
WINCHESTER, B
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,30 GUILFORD ST,LONDON WC1N 1EH,ENGLAND
WINCHESTER, B
.
ARCHIVES OF DISEASE IN CHILDHOOD,
1991,
66
(09)
:1027
-1032
[4]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN-SYNDROME TYPE-II - A DEFICIENCY IN GOLGI LOCALIZED N-ACETYL-GLUCOSAMINYLTRANSFERASE-II
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
JAEKEN, J
;
SCHACHTER, H
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
SCHACHTER, H
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
CARCHON, H
;
DECOCK, P
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
DECOCK, P
;
CODDEVILLE, B
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
CODDEVILLE, B
;
SPIK, G
论文数:
0
引用数:
0
h-index:
0
机构:
HOSP SICK CHILDREN,DEPT BIOCHEM RES,TORONTO M5G 1X8,ON,CANADA
SPIK, G
.
ARCHIVES OF DISEASE IN CHILDHOOD,
1994,
71
(02)
:123
-127
[5]
THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - PRE-GOLGI AND GOLGI DISORDERS
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
JAEKEN, J
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
CARCHON, H
;
STIBLER, H
论文数:
0
引用数:
0
h-index:
0
机构:
CATHOLIC UNIV LEUVEN,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
STIBLER, H
.
GLYCOBIOLOGY,
1993,
3
(05)
:423
-428
[6]
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-II
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
JAEKEN, J
;
DECOCK, P
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
DECOCK, P
;
STIBLER, H
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
STIBLER, H
;
VANGEET, C
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
VANGEET, C
;
KINT, J
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
KINT, J
;
RAMAEKERS, V
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
RAMAEKERS, V
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
KAROLINSKA INST,DEPT NEUROL,STOCKHOLM,SWEDEN
CARCHON, H
.
JOURNAL OF INHERITED METABOLIC DISEASE,
1993,
16
(06)
:1041
-1041
[7]
THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - AN OVERVIEW
[J].
JAEKEN, J
论文数:
0
引用数:
0
h-index:
0
机构:
Centre for Metabolic Diseases, Department of Pediatrics, University of Leuven
JAEKEN, J
;
CARCHON, H
论文数:
0
引用数:
0
h-index:
0
机构:
Centre for Metabolic Diseases, Department of Pediatrics, University of Leuven
CARCHON, H
.
JOURNAL OF INHERITED METABOLIC DISEASE,
1993,
16
(05)
:813
-820
[8]
SERUM LYSOSOMAL-ENZYME ABNORMALITIES IN GALACTOSEMIA
[J].
JAEKEN, J
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