- ►diabetesjournals.org M Rafiq, SE Flanagan, AM Patch, BM Shields, S … - 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 diabetes due ... Cited by 19 - Related articles - BL Direct - All 5 versions
AM Patch, SE Flanagan, C Boustred, AT … - Diabetes Obes …, 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 ... Cited by 4 - Related articles - All 21 versions
EL Edghill, SE Flanagan, AM Patch, C Boustred, A … - 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) account for ... Cited by 30 - Related articles - BL Direct - All 5 versions
- ►angrylapdog.com S Suzuki, Y Makita, T Mukai, K … - Journal of …, 2007 - jcem.endojournals.org.p. … 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, J … - Journal of Clinical …, 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 ... Cited by 30 - Related articles - BL Direct - All 4 versions
- ►diabetesjournals.org M Polak, A Dechaume, H Cavé, R Nimri, H Crosnier, V … - 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 encode the ... Cited by 12 - Related articles - BL Direct - All 5 versions
AI Tarasov, CA Girard, B Larkin, P Tammaro, … - Diabetes Obes …, 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 ... Cited by 2 - Related articles - All 2 versions
