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Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.
Am J Med Genet A. 2024 Jun;194(6):e63533. doi: 10.1002/ajmg.a.63533. Epub 2024 Jan 17.
Am J Med Genet A. 2024.
PMID: 38234231
Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes.
Johnson MB, De Franco E, Lango Allen H, Al Senani A, Elbarbary N, Siklar Z, Berberoglu M, Imane Z, Haghighi A, Razavi Z, Ullah I, Alyaarubi S, Gardner D, Ellard S, Hattersley AT, Flanagan SE.
Johnson MB, et al. Among authors: al senani a.
Diabetes. 2017 Aug;66(8):2316-2322. doi: 10.2337/db17-0040. Epub 2017 May 4.
Diabetes. 2017.
PMID: 28473463
Free PMC article.
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Genetic mutations associated with neonatal diabetes mellitus in Omani patients.
Al Senani A, Hamza N, Al Azkawi H, Al Kharusi M, Al Sukaiti N, Al Badi M, Al Yahyai M, Johnson M, De Franco E, Flanagan S, Hattersley A, Ellard S, Mula-Abed WA.
Al Senani A, et al.
J Pediatr Endocrinol Metab. 2018 Jan 26;31(2):195-204. doi: 10.1515/jpem-2017-0284.
J Pediatr Endocrinol Metab. 2018.
PMID: 29329106
Free PMC article.
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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience.
Al-Badi MK, Al-Azkawi HS, Al-Yahyaei MS, Mula-Abed WA, Al-Senani AM.
Al-Badi MK, et al. Among authors: al senani am.
Saudi Med J. 2019 Jul;40(7):669-674. doi: 10.15537/smj.2019.7.24291.
Saudi Med J. 2019.
PMID: 31287126
Free PMC article.
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Demographic Features and Etiology of Congenital Hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016.
Al Jafari M, Jose S, Al Senani A.
Al Jafari M, et al. Among authors: al senani a.
Oman Med J. 2020 Sep 30;35(5):e171. doi: 10.5001/omj.2020.113. eCollection 2020 Sep.
Oman Med J. 2020.
PMID: 33062310
Free PMC article.
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Erratum. Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 2017;66:2316-2322.
Johnson MB, De Franco E, Lango Allen H, Al Senani A, Elbarbary N, Siklar Z, Berberoglu M, Imane Z, Haghighi A, Razavi Z, Ullah I, Alyaarubi S, Gardner D, Ellard S, Hattersley AT, Flanagan SE.
Johnson MB, et al. Among authors: al senani a.
Diabetes. 2018 Mar;67(3):532. doi: 10.2337/db18-er03b. Epub 2018 Jan 5.
Diabetes. 2018.
PMID: 29305528
Free PMC article.
No abstract available.
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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.
Yau M, Haider S, Khattab A, Ling C, Mathew M, Zaidi S, Bloch M, Patel M, Ewert S, Abdullah W, Toygar A, Mudryi V, Al Badi M, Alzubdi M, Wilson RC, Al Azkawi HS, Ozdemir HN, Abu-Amer W, Hertecant J, Razzaghy-Azar M, Funder JW, Al Senani A, Sun L, Kim SM, Yuen T, Zaidi M, New MI.
Yau M, et al. Among authors: al senani a.
Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):E11248-E11256. doi: 10.1073/pnas.1716621115. Epub 2017 Dec 11.
Proc Natl Acad Sci U S A. 2017.
PMID: 29229831
Free PMC article.
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SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.
Sansbury FH, Flanagan SE, Houghton JA, Shuixian Shen FL, Al-Senani AM, Habeb AM, Abdullah M, Kariminejad A, Ellard S, Hattersley AT.
Sansbury FH, et al. Among authors: al senani am.
Diabetologia. 2012 Sep;55(9):2381-5. doi: 10.1007/s00125-012-2595-0. Epub 2012 Jun 2.
Diabetologia. 2012.
PMID: 22660720
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