Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes

被引：30

作者：

Gloyn, AL ^{[1
]}

Ellard, S ^{[1
]}

Shield, JP ^{[1
]}

Temple, IK ^{[1
]}

Mackay, DJC ^{[1
]}

Polak, M ^{[1
]}

Barrett, T ^{[1
]}

Hattersley, AT ^{[1
]}

机构：

[1] Univ Exeter, Sch Postgrad Med & Hlth Sci, Ctr Genet Mol, Exeter EX2 5AX, Devon, England

来源：

DIABETOLOGIA | 2002年 / 45卷 / 02期

关键词：

Gestational Diabetes; Islet Cell Antibody; Neonatal Diabetes; Neonatal Diabetes Mellitus; Permanent Neonatal Diabetes;

D O I：

10.1007/s00125-001-0746-9

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：290 / 290

页数：1

共 8 条

[1] EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
Delépine, M
Nicolino, M
Barrett, T
Golamaully, M
Lathrop, GM
Julier, C
[J]. NATURE GENETICS, 2000, 25 (04) : 406 - 409
[2] A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria
Ellard, S
Beards, F
Allen, LIS
Shepherd, M
Ballantyne, E
Harvey, R
Hattersley, AT
[J]. DIABETOLOGIA, 2000, 43 (02) : 250 - 253
[3] FAMILIAL HYPERGLYCEMIA DUE TO MUTATIONS IN GLUCOKINASE - DEFINITION OF A SUBTYPE OF DIABETES-MELLITUS
FROGUEL, P
ZOUALI, H
VIONNET, N
VELHO, G
VAXILLAIRE, M
SUN, F
LESAGE, S
STOFFEL, M
TAKEDA, J
PASSA, P
PERMUTT, MA
BECKMANN, JS
BELL, GI
COHEN, D
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (10) : 697 - 702
[4] Neonatal diabetes mellitus due to complete glucokinase deficiency.
Njolstad, PR
Sovik, O
Cuesta-Muñoz, A
Bjorkhaug, L
Massa, O
Barbetti, F
Undlien, DE
Shiota, C
Magnuson, MA
Molven, A
Matschinsky, FM
Bell, GI
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (21) : 1588 - 1592
[5] SHIELD JPH, 1996, BAILLIERES CLIN PAED, P681
[6] Transient neonatal diabetes - Widening the understanding of the etiopathogenesis of diabetes
Temple, IK
Gardner, RJ
Mackay, DJG
Barber, JCK
Robinson, DO
Shield, JPH
[J]. DIABETES, 2000, 49 (08) : 1359 - 1366
[7] LONG-TERM COURSE OF NEONATAL DIABETES
VONMUHLENDAHL, E
HERKENHOFF, H
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (11) : 704 - 708
[8] X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
Wildin, RS
Ramsdell, F
Peake, J
Faravelli, F
Casanova, JL
Buist, N
Levy-Lahad, E
Mazzella, M
Goulet, O
Perroni, L
Bricarelli, FD
Byrne, G
McEuen, M
Proll, S
Appleby, M
Brunkow, ME
[J]. NATURE GENETICS, 2001, 27 (01) : 18 - 20

← 1 →