- ►diabetesjournals.org M Rafiq, SE Flanagan, AM Patch, BM Shields, … - Diabetes Care, 2008 - Am Diabetes Assoc OBJECTIVE—Neonatal diabetes can result from mutations in the Kir6.2 or
sulfonylurea receptor 1 (SUR1) subunits of the ATP-sensitive K + channel.
Transfer from insulin to oral sulfonylureas in patients with neonatal ... Cited by 19 - Related articles - BL Direct - All 5 versions
AM Patch, SE Flanagan, C Boustred, AT … - Diabetes Obes Metab, 2007 - 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 9 - Related articles - All 3 versions
H Zhang, X Liu, H Kuang, R Yi, H Xing - Diabetes research and clinical practice, 2007 - Elsevier Type 2 diabetes is a heterogeneous disorder that results from impaired insulin
secretion and insulin action [1] and [2]. The significant association between
sulfonylurea receptor 1 (SUR1) gene polymorphisms and type 2 diabetes has ... Cited by 4 - Related articles - All 21 versions
EL Edghill, SE Flanagan, AM Patch, C Boustred … - Diabetes, 2008 - Am Diabetes Assoc RESULTS— We identified heterozygous INS mutations in 33 of 141 probands
diagnosed at <6 months, 2 of 86 between 6 and 12 months, and none of 58 between
12 and 24 months of age. Three known mutations (A24D, F48C, and R89C) ... Cited by 30 - Related articles - BL Direct - All 5 versions
- ►angrylapdog.com S Suzuki, Y Makita, T Mukai, K Matsuo, O … - Journal of Clinical Endocrinology & Metabolism, 2007 - jcem.endojournals.org.p.angrylapdog.com Results: A molecular basis for NDM was found in 23 patients: 6q24 in eleven,
KCNJ11 in nine, ABCC8 in two, and FOXP3 in one. All the patients with the 6q24
abnormality and two patients with the KCNJ11 mutation proved to be TNDM. ... Cited by 8 - Related articles - BL Direct - All 4 versions
- ►endojournals.org J Stanik, D Gasperikova, M Paskova, L Barak, … - Journal of Clinical Endocrinology & Metabolism, 2007 - Endocrine Soc Context: Mutations in the KCNJ11 and ABCC8 genes encoding the pancreatic ß-cell
K ATP channel have recently been shown to be the most common cause of permanent
neonatal diabetes mellitus (PNDM). Information regarding the frequency of ... Cited by 30 - Related articles - BL Direct - All 4 versions
- ►diabetesjournals.org M Polak, A Dechaume, H Cavé, R Nimri, H … - Diabetes, 2008 - Am Diabetes Assoc OBJECTIVE—Permanent neonatal diabetes (PND) is defined by chronic
hyperglycemia due to severe nonautoimmune insulin deficiency diagnosed in the
first months of life. Several genes, including KCNJ11 and ABCC8, which ... Cited by 12 - Related articles - BL Direct - All 5 versions
AI Tarasov, CA Girard, B Larkin, P Tammaro, … - Diabetes Obes Metab, 2007 - interscience.wiley.com Heterozygous activating mutations in Kir6.2 (KCNJ11), the pore-forming subunit
of the adenosine triphosphate (ATP)-sensitive potassium (K ATP ) channel, are a
common cause of neonatal diabetes (ND). We assessed the functional effects ... Cited by 2 - Related articles - All 2 versions
