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Suggested authors matching "AUTH:Al Senani A" with an ORCID

Aisha Al Senani
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Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.
Akinci G, Alyaarubi S, Patni N, Alhashmi N, Al-Shidhani A, Prodam F, Gagne N, Babalola F, Al Senani A, Muniraj K, Elsayed SM, Beghini M, Saydam BO, Allawati M, Vaishnav MS, Can E, Simsir IY, Sorkina E, Dursun F, [...] Garg A
Am J Med Genet A, 194(6):e63533, 17 Jan 2024
Cited by: 2 articles | PMID: 38234231
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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
Oman Med J, 35(5):e171, 30 Sep 2020
Cited by: 1 article | PMID: 33062310 | PMCID: PMC7533048
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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
Saudi Med J, 40(7):669-674, 01 Jul 2019
Cited by: 1 article | PMID: 31287126 | PMCID: PMC6757195
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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
Diabetes, 67(3):532, 05 Jan 2018
Cited by: 0 articles | PMID: 29305528 | PMCID: PMC5828457
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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
J Pediatr Endocrinol Metab, 31(2):195-204, 01 Jan 2018
Cited by: 5 articles | PMID: 29329106 | PMCID: PMC6853791
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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, [...] New MI
Proc Natl Acad Sci U S A, 114(52):E11248-E11256, 11 Dec 2017
Cited by: 25 articles | PMID: 29229831 | PMCID: PMC5748222
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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
Diabetes, 66(8):2316-2322, 04 May 2017
Cited by: 35 articles | PMID: 28473463 | PMCID: PMC5524180
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2nd Genetics Conference: Genetics in developing countries, unique challenges and opportunities : Sultan Qaboos University, 9–11 March 2014
Al-Mjeni R, Bainbridge M, Al-Kharousi N, Al-Senawi R, Muzny D, Al-Mohammedawi D, Ganesh A, Gibbs R, Gingras M, Al-Yahyaee S, Al-Sukaiti N, Al-Hashmi N, Al-Shehhi M, Al-Rawas A, Wali Y, Al-Araimi M, Pal B, Poulter J, van Genderen M, [...] Al-Ajmi A
Sultan Qaboos Univ Med J, 14(4):E593-E602, 14 Oct 2014
Cited by: 0 articles | PMCID: PMC4214570
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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
Diabetologia, 55(9):2381-2385, 02 Jun 2012
Cited by: 64 articles | PMID: 22660720
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1-9 of 9 results

Search life-sciences literature (45,103,589 articles, preprints and more)

Suggested authors matching "AUTH:Al Senani A" with an ORCID

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Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.

Demographic Features and Etiology of Congenital Hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016.

Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience.

Erratum. Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 2017;66:2316-2322.

Genetic mutations associated with neonatal diabetes mellitus in Omani patients.

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes.

2nd Genetics Conference: Genetics in developing countries, unique challenges and opportunities : Sultan Qaboos University, 9–11 March 2014

SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.

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Suggested authors matching "AUTH:Al Senani A" with an ORCID