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Scholar Results 1 - 10 of about 101 related to Esmatjes: Neonatal Diabetes With End-Stage Nephropathy. (0.14 sec) 

Neonatal Diabetes With End-Stage Nephropathy


E Esmatjes, A Jimenez, G Diaz, M Mora, R … - Diabetes Care, 2008 - Am Diabetes Assoc
OBJECTIVE—To describe the diagnosis of a patient with neonatal diabetes who
had been misdiagnosed with type 1 diabetes and referred to our hospital for
pancreas and kidney transplantation because of end-stage renal disease.
Related articles - All 3 versions

Sulfonylurea Treatment in Young Children With Neonatal Diabetes


E Codner, SE Flanagan, F Ugarte, H García, T … - Diabetes Care, 2007 - Am Diabetes Assoc
In case 1, a girl was transferred from insulin to glibenclamide at 17 months (7)
and had been on this treatment for 2 years. During this period, blood glucose
testing decreased from 5–6 to 2–3 tests/day. As blood glucose levels ...
Cited by 12 - Related articles - All 5 versions

Sulfonylurea Treatment in Young Children with Neonatal Diabetes: Dealing with …


MD Ethel Codner, SEF BSc, MD Francisca … - Diabetes Care - Am Diabetes Assoc
Ethel Codner, MD1, Sarah E. Flanagan BSc2, Francisca Ugarte, MD3, Hernán
García, MD4, Teresa Vidal, MD5, Sian Ellard PhD2 MRCPath, Andrew T. Hattersley,
DM, FRCP2. 1: Institute of Maternal and Child Research, School of Medicine, ...
Related articles - All 2 versions

Transfer to Sulphonylurea Therapy in Adult Subjects With Permanent Neonatal Diabetes …


MT Malecki, J Skupien, T Klupa, K Wanic, W … - Diabetes Care, 2007 - Am Diabetes Assoc
Activating mutations in the KCJN11 gene encoding in the ATP-sensitive K +
channel (K ATP channel) subunit Kir6.2 were reported (1) as the most common
cause of permanent neonatal diabetes (PND). Recently, it has been shown ...
Cited by 11 - Related articles - All 4 versions

[CITATION] Sulphonylurea treatment does not improve psychomotor development in children with …


Z Sumnik, S Kolouskova, JK Wales, V … - Diabetic medicine: a journal of the British Diabetic …, 2007 - ncbi.nlm.nih.gov
1: Diabet Med. 2007 Oct;24(10):1176-8. Sulphonylurea treatment does not
improve psychomotor development in children with KCNJ11 ...
Cited by 2 - Related articles - BL Direct - All 3 versions

Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a …


W Mlynarski, AI Tarasov, A Gach, CA Girard, I … - Nature Clinical Practice Neurology, 2007 - medscape.com
A female infant presented with polydipsia, glucosuria, ketoacidosis (pH 7.09,
-14 mmol/l base excess) and severe hyperglycemia (blood glucose 42.5 mmol/l [766
mg/dl]) 12 weeks after birth. C peptide was undetectable. Tests for islet ...
Cited by 11 - Related articles - BL Direct - All 6 versions

Type 2 diabetic patients with nephropathy in a Scandinavian kidney-transplant population


G Nyberg, M Hartsoe, L Mjörnstedt, G Norden - Scandinavian journal of urology and nephrology, 1996 - cat.inist.fr
Twenty-seven patients in a cohort of 1000 who received kidney transplants in
Göteborg 1985-1993 were found to have diabetes of Type 2 as primary cause of
renal failure. All took insulin at the time of transplantation. Four ...
Cited by 16 - Related articles - BL Direct - All 2 versions

Mutations in the ABCC8 gene are associated with a variable clinical phenotype


T Klupa, I Kowalska, K Wyka, J Skupien, AM … - Clin Endocrinol (Oxf), 2008 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ...
Cited by 2 - Related articles - All 3 versions

Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 …


VM Wagner, B Kremke, O Hiort, SE Flanagan … - European Journal of Pediatrics, 2009 - Springer
Page 1. SHORT REPORT Transition from insulin to sulfonylurea in a child
with diabetes due to a mutation in KCNJ11 encoding Kir6.2 ...
Cited by 1 - Related articles - All 2 versions

[PDF] Norsk forskning


D i Bergen2079 - J Med, 2006 - tidsskriftet.no
Heterozygote, aktiverende mutasjoner i genet KCNJ11 forårsaker 30–60 % av
til- fellene av diabetes før seks måneders alder. Sykdommen debuterer da med
ketoacidose eller alvorlig hyperglykemi. Man har derfor ment at det dreier ...
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