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1999 2
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Page 1
Monogenic Forms of Diabetes Mellitus.
Gaál Z, Balogh I. Gaál Z, et al. Exp Suppl. 2019;111:385-416. doi: 10.1007/978-3-030-25905-1_18. Exp Suppl. 2019. PMID: 31588541 Review.
The hyperglycemia usually requires insulin. There are two forms, permanent neonatal diabetes mellitus (PNDM) and transient neonatal diabetes mellitus (TNDM). ...
The hyperglycemia usually requires insulin. There are two forms, permanent neonatal diabetes mellitus (PNDM) and …
Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study.
Kanakatti Shankar R, Pihoker C, Dolan LM, Standiford D, Badaru A, Dabelea D, Rodriguez B, Black MH, Imperatore G, Hattersley A, Ellard S, Gilliam LK; SEARCH for Diabetes in Youth Study Group. Kanakatti Shankar R, et al. Pediatr Diabetes. 2013 May;14(3):174-80. doi: 10.1111/pedi.12003. Epub 2012 Oct 10. Pediatr Diabetes. 2013. PMID: 23050777 Free PMC article.
BACKGROUND: Neonatal diabetes mellitus (NDM) is defined as diabetes with onset before 6 months of age. Nearly half of individuals with NDM are affected by permanent neonatal diabetes mellitus (PNDM). Mutations in KATP channel genes (KCNJ11, ABCC8) and …
BACKGROUND: Neonatal diabetes mellitus (NDM) is defined as diabetes with onset before 6 months of age. Nearly half of individuals with NDM a …
Clinical features and partial proportional molecular genetics in neonatal diabetes mellitus: a retrospective analysis in southwestern China.
Cao L, He Y, Huang Q, Zhang Y, Deng P, Du W, Hua Z, Zhu M, Wei H. Cao L, et al. Endocrine. 2020 Jul;69(1):53-62. doi: 10.1007/s12020-020-02279-4. Epub 2020 Apr 11. Endocrine. 2020. PMID: 32279225
Peripheral blood samples of the patients and their parents were collected for mutation detection. RESULTS: Among the 16 cases of NDM, 8 cases were permanent neonatal diabetes mellitus (PNDM) (including 3 clinical syndromes), and 3 cases were transient …
Peripheral blood samples of the patients and their parents were collected for mutation detection. RESULTS: Among the 16 cases of NDM, 8 case …
Permanent neonatal diabetes mellitus: clinical presentation and epidemiology in Oman.
Bappal B, Raghupathy P, de Silva V, Khusaiby SM. Bappal B, et al. Arch Dis Child Fetal Neonatal Ed. 1999 May;80(3):F209-12. doi: 10.1136/fn.80.3.f209. Arch Dis Child Fetal Neonatal Ed. 1999. PMID: 10212083 Free PMC article.
AIM: To estimate the accurate incidence and prevalence of permanent neonatal diabetes mellitus, and to determine the clinical profile of this condition in the Sultanate of Oman. METHODS: All children diagnosed as having permanent neonatal
AIM: To estimate the accurate incidence and prevalence of permanent neonatal diabetes mellitus, and to determine …
Permanent neonatal diabetes mellitus: epidemiology, mode of presentation, pathogenesis and growth.
Soliman AT, elZalabany MM, Bappal B, alSalmi I, de Silva V, Asfour M. Soliman AT, et al. Indian J Pediatr. 1999 May-Jun;66(3):363-73. doi: 10.1007/BF02845526. Indian J Pediatr. 1999. PMID: 10798084
Permanent neonatal diabetes mellitus (PNIDDM) is a rare form of IDDM with unclear etiology and pathogenesis. ...
Permanent neonatal diabetes mellitus (PNIDDM) is a rare form of IDDM with unclear etiology and pathogenesis. ...
Transient but not permanent neonatal diabetes mellitus is associated with paternal uniparental isodisomy of chromosome 6.
Hermann R, Laine AP, Johansson C, Niederland T, Tokarska L, Dziatkowiak H, Ilonen J, Soltész G. Hermann R, et al. Pediatrics. 2000 Jan;105(1 Pt 1):49-52. doi: 10.1542/peds.105.1.49. Pediatrics. 2000. PMID: 10617703
OBJECTIVES: The factors determining the pathogenesis of transient and permanent neonatal diabetes mellitus are poorly characterized. The purpose of this study was to examine the role of chromosome 6 in the pathogenesis of neonatal diabetes mellitus and …
OBJECTIVES: The factors determining the pathogenesis of transient and permanent neonatal diabetes mellitus are p …
ADHD, learning difficulties and sleep disturbances associated with KCNJ11-related neonatal diabetes.
Landmeier KA, Lanning M, Carmody D, Greeley SAW, Msall ME. Landmeier KA, et al. Pediatr Diabetes. 2017 Nov;18(7):518-523. doi: 10.1111/pedi.12428. Epub 2016 Aug 24. Pediatr Diabetes. 2017. PMID: 27555491 Free PMC article.
OBJECTIVES: Mutations in KCNJ11 are the most common cause of permanent neonatal diabetes mellitus (NDM). Approximately 25% of patients have obvious neurological dysfunction, but whether milder related problems might be more common has been unclear. ...
OBJECTIVES: Mutations in KCNJ11 are the most common cause of permanent neonatal diabetes mellitus (NDM). Approxi …
Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans.
Habeb AM, Flanagan SE, Deeb A, Al-Alwan I, Alawneh H, Balafrej AA, Mutair A, Hattersley AT, Hussain K, Ellard S. Habeb AM, et al. Arch Dis Child. 2012 Aug;97(8):721-3. doi: 10.1136/archdischild-2012-301744. Arch Dis Child. 2012. PMID: 22859427
OBJECTIVE: Mutations in the KCNJ11 and ABCC8 genes that encode the pancreatic K(ATP) channel are the commonest cause of permanent neonatal diabetes mellitus (PNDM). The authors aimed to define the genetic causes of PNDM in a large cohort of Arab patien …
OBJECTIVE: Mutations in the KCNJ11 and ABCC8 genes that encode the pancreatic K(ATP) channel are the commonest cause of permanent
Wolcott-Rallison syndrome: a case series of three patients.
Memon F, Arif M, Kirmani S, Humayun K. Memon F, et al. Pediatr Endocrinol Diabetes Metab. 2022;28(3):238-240. doi: 10.5114/pedm.2022.118325. Pediatr Endocrinol Diabetes Metab. 2022. PMID: 36106422 Free PMC article.
31 results