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Quoted phrase not found in phrase index: "Diabetes mellitus, permanent neonatal 3"
Page 1
Meglitinide (repaglinide) therapy in permanent neonatal diabetes mellitus: two case reports.
Razzaghy-Azar M, Nourbakhsh M, Talea A, Mohammad Amoli M, Nourbakhsh M, Larijani B. Razzaghy-Azar M, et al. J Med Case Rep. 2021 Oct 25;15(1):535. doi: 10.1186/s13256-021-03052-5. J Med Case Rep. 2021. PMID: 34696808 Free PMC article.
We report herein the effects of repaglinide administration in the management and clinical outcome of two patients with PNDM during 9 and 10 years of follow-up. ...The values of self-monitored blood glucose were well-controlled, and the hemoglobin A1C (HbA1C) levels ranged …
We report herein the effects of repaglinide administration in the management and clinical outcome of two patients with PNDM during 9 …
Neonatal Diabetes Mellitus - Is Trisomy 21 Associated With Refractory Hyperglycaemia?
Mirza A, Dhillon RA, Irfan O, Amin A, Salat M. Mirza A, et al. J Ayub Med Coll Abbottabad. 2022 Jul-Sep;34(Suppl 1)(3):S717-S719. doi: 10.55519/JAMC-03-S1-9858. J Ayub Med Coll Abbottabad. 2022. PMID: 36414599 Free article.
CONCLUSION: Neonates with diabetes mellitus usually present with clinical features such as low-birth weight, ketoacidosis, consistent insulin-requiring hyperglycaemia and preterm. ...
CONCLUSION: Neonates with diabetes mellitus usually present with clinical features such as low-birth weight, ketoacidosis, consistent …
Molecular and clinical features of K(ATP) -channel neonatal diabetes mellitus in Japan.
Hashimoto Y, Dateki S, Hirose M, Satomura K, Sawada H, Mizuno H, Sugihara S, Maruyama K, Urakami T, Sugawara H, Shirai K, Yorifuji T. Hashimoto Y, et al. Pediatr Diabetes. 2017 Nov;18(7):532-539. doi: 10.1111/pedi.12447. Epub 2016 Sep 29. Pediatr Diabetes. 2017. PMID: 27681997
Mutations in ABCC8 were associated with TNDM (4/9) or isolated PNDM (5/9), whereas those in KCNJ11 were associated with more severe phenotypes, including DEND (3/16), iDEND (intermediate DEND, 4/16), or isolated PNDM (6/16). ...Three others with iDEND mutations (R201C, G53 …
Mutations in ABCC8 were associated with TNDM (4/9) or isolated PNDM (5/9), whereas those in KCNJ11 were associated with more severe phenotyp …
The quality of reporting in case reports of permanent neonatal diabetes mellitus: a cross-sectional study.
Jia P, Wang L, Yang X, Pei W, Xu C, Feng J, Han Y. Jia P, et al. BMC Med Res Methodol. 2024 May 20;24(1):117. doi: 10.1186/s12874-024-02226-1. BMC Med Res Methodol. 2024. PMID: 38769533 Free PMC article.
The predictor variables were impact factor of the published journal (<3.4 vs. 3.4, categorized according to the median), funding (yes vs. no), language (English vs. other language), published journal type (general vs. special) and year of publication (>2013 vs …
The predictor variables were impact factor of the published journal (<3.4 vs. 3.4, categorized according to the median), fu …
Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K(ATP)-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC. Ngoc CTB, et al. Front Endocrinol (Lausanne). 2021 Sep 9;12:727083. doi: 10.3389/fendo.2021.727083. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34566892 Free PMC article.
Overall, 51% had low birth weight (below 3rd percentile), 23 (85%) were diagnosed before 3 months of age, and 23 (85%) presented with diabetic ketoacidosis. At diagnosis, clinical and biochemical findings (mean SD) were pH 7.16 0.16; HCO3- , 7.9 7.4 mmol/L; BE, -17. …
Overall, 51% had low birth weight (below 3rd percentile), 23 (85%) were diagnosed before 3 months of age, and 23 (85%) presented with …
Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India.
Jain V, Satapathy A, Yadav J, Sharma R, Radha V, Mohan V, De Franco E, Ellard S. Jain V, et al. Indian Pediatr. 2017 Jun 15;54(6):467-471. doi: 10.1007/s13312-017-1049-7. Indian Pediatr. 2017. PMID: 28667717 Free article.
OBJECTIVE: To study the genetic mutations and clinical profile in children with neonatal diabetes mellitus. METHODS: Genetic evaluation, clinical management and follow-up of infants with neonatal diabetes. ...CONCLUSION: Neonatal diabetes mellitus is a heterogeneous …
OBJECTIVE: To study the genetic mutations and clinical profile in children with neonatal diabetes mellitus. METHODS: Genetic evaluati …
Early transition from insulin to sulfonylureas in neonatal diabetes and follow-up: Experience from China.
Li X, Xu A, Sheng H, Ting TH, Mao X, Huang X, Jiang M, Cheng J, Liu L. Li X, et al. Pediatr Diabetes. 2018 Mar;19(2):251-258. doi: 10.1111/pedi.12560. Epub 2017 Aug 8. Pediatr Diabetes. 2018. PMID: 28791793
RESULTS: There were 23 NDM patients from 22 unrelated families, 10 had KCNJ11 mutations, 3 harbored ABCC8 mutations, 1 had INS mutations, 4 had chromosome 6q24 abnormalities, 1 had a deletion at chromosome 1p36.23p36.12, and 4 had no genetic abnormality identified. ...A to …
RESULTS: There were 23 NDM patients from 22 unrelated families, 10 had KCNJ11 mutations, 3 harbored ABCC8 mutations, 1 had INS mutati …
Successful off-label sulfonylurea treatment of neonatal diabetes mellitus due to chromosome 6 abnormalities.
Garcin L, Kariyawasam D, Busiah K, Fauret-Amsellem AL, Le Bourgeois F, Vaivre-Douret L, Cavé H, Polak M, Beltrand J. Garcin L, et al. Pediatr Diabetes. 2018 Jun;19(4):663-669. doi: 10.1111/pedi.12635. Epub 2018 Mar 4. Pediatr Diabetes. 2018. PMID: 29504184 Review.
Our objective was to evaluate the efficacy and safety of SU therapy in chromosome 6-related TNDM. Description of 3 case reports and literature review was the subject of the study. ...
Our objective was to evaluate the efficacy and safety of SU therapy in chromosome 6-related TNDM. Description of 3 case reports and l …
Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations.
Beltrand J, Elie C, Busiah K, Fournier E, Boddaert N, Bahi-Buisson N, Vera M, Bui-Quoc E, Ingster-Moati I, Berdugo M, Simon A, Gozalo C, Djerada Z, Flechtner I, Treluyer JM, Scharfmann R, Cavé H, Vaivre-Douret L, Polak M; GlidKir Study Group. Beltrand J, et al. Diabetes Care. 2015 Nov;38(11):2033-41. doi: 10.2337/dc15-0837. Epub 2015 Oct 5. Diabetes Care. 2015. PMID: 26438614 Clinical Trial.

RESULTS: At baseline, hypotonia, deficiencies in gesture conception or realization, and attention disorders were common. SU improved HbA1c levels (median change -1.55% [range -3.8 to 0.1]; P < 0.0001), intelligence scores, hypotonia (in 12 of 15 patients), visual attent

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RESULTS: At baseline, hypotonia, deficiencies in gesture conception or realization, and attention disorders were common. SU improved HbA1c l …
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