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1.
Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation.
Diabet Med
; 25(3): 277-81, 2008 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-18307455
2.
Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation.
Diabetologia
; 54(2): 469-71, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21109997
3.
[From gene to disease; neonatal diabetes mellitus and the KCNJ11 gene]. / Van gen naar ziekte; neonatale diabetes mellitus en het KCNJ11-gen.
Ned Tijdschr Geneeskd
; 149(49): 2732-6, 2005 Dec 03.
Artículo
en Neerlandesa
| MEDLINE | ID: mdl-16375017
4.
Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.
Diabetologia
; 52(8): 1683-5, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19499210
5.
[Two children with extrapulmonary symptoms due to tuberculosis]. / Twee kinderen met extrapulmonale klachten door tuberculose.
Ned Tijdschr Geneeskd
; 145(3): 113-5, 2001 Jan 20.
Artículo
en Neerlandesa
| MEDLINE | ID: mdl-11206119
6.
The relation between non-occupational physical activity and years lived with and without disability.
J Epidemiol Community Health
; 62(9): 823-8, 2008 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-18701734
7.
Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene.
Diabetologia
; 49(11): 2559-63, 2006 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-17047922
8.
Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development.
Diabet Med
; 23(12): 1301-6, 2006 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-17116179
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