Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aisha Al senani"'
Autor:
Asma Deeb, Jean-Pierre Chanoine, Jamal Raza, Amanda Rowlands, Abdulsalam Abu-Libdeh, Asmahane Ladjouze, Rasha T Hamza, Salwa A Musa, Farida Jennane, Bouferoua Fadila, Delileche Hana, Djahlat Larbi, Noumi Mustapha, Haya Alkhayyat, Abdourahman Douksie, Ali Rabbani, Ali Al-Jumaili, Rasha Odeh, Hessa Alkandari, Hala Tfayli, Suleiman Abusrewil, Millad Ghawil, Aisha Al senani, Fawziya Alkhalaf, Abdelhadi Habeb, Noman Ahmad, Omer Elshareef, Mohamed Abdullah, Olivia Al-Hassan, Dima Karah, Mongia Hachicha, Mohammed Alshakka
Publikováno v:
BMJ Global Health, Vol 6, Iss 10 (2021)
Congenital adrenal hyperplasia (CAH), if untreated, carries high morbidity and mortality. A higher incidence of CAH is expected in countries where consanguinity is common, such as in the countries of the WHO Eastern Mediterranean Region (EMRO). CAH i
Externí odkaz:
https://doaj.org/article/56dbc542be5c46a880a38a1bb10953e1
Publikováno v:
Oman Medical Journal, Vol 35, Iss 5, Pp e171-e171 (2020)
Objectives: Congenital hypothyroidism (CH) is the most common endocrine disorder in neonates as well as one of the few preventable causes of severe learning difficulties. Early screening, diagnosis, and treatment are mandatory to prevent later sequel
Externí odkaz:
https://doaj.org/article/c9e03be3293a49eda91b988a9f4ea160
Autor:
Andrew T. Hattersley, Maryam Al Badi, Waad-Allah Mula-Abed, Sarah E. Flanagan, Moza Al Yahyai, Manal Al Kharusi, Nishath Hamza, Aisha Al Senani, Sian Ellard, Hanan Said Al Azkawi, Matthew B. Johnson, Nashat Al Sukaiti, Elisa De Franco
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:195-204
Background:Neonatal diabetes mellitus (NDM) is a rare disorder worldwide where diabetes is diagnosed in the first 6 months of life. However, Oman has a relatively high incidence of NDM.Methods:In this study, we investigated the genetic etiologies und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e115059e4fde8a6a94185e7d9d0daf
https://doi.org/10.1515/jpem-2017-0284
https://doi.org/10.1515/jpem-2017-0284
Autor:
Ahmed Khattab, Wafa Abdullah, Robert C. Wilson, Tony Yuen, Shozeb Haider, Maryam Al Badi, Aisha Al Senani, Hanan Said Al Azkawi, Mone Zaidi, Maria I. New, Mabel Yau
Publikováno v:
Annals of the New York Academy of Sciences. 1376:65-71
Apparent mineralocorticoid excess (AME) is a rare autosomal recessive genetic disorder causing severe hypertension in childhood due to a deficiency of 11β-hydroxysteroid dehydrogenase type 2 (11βHSD2), which is encoded by HSD11B2. Without treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6ce49eec087c32dcf13cabf0b8bad71
https://doi.org/10.1111/nyas.13162
https://doi.org/10.1111/nyas.13162
Autor:
Tony Yuen, John W Funder, Chen Ling, Maryam Al Badi, Vitalii Mudryi, Maria I. New, Mone Zaidi, Robert C. Wilson, Se-Min Kim, Maryam Razzaghy-Azar, Hatice Nur Ozdemir, Mabel Yau, Aysenur Toygar, Jozef Hertecant, Mehr Mathew, Madison Bloch, Wafa Abdullah, Shozeb Haider, Samir Zaidi, Sinead Ewert, Aisha Al Senani, Hanan Said Al Azkawi, Monica Patel, Wahid Abu-Amer, Mouch Alzubdi, Ahmed Khattab, Li Sun
Publikováno v:
Proceedings of the National Academy of Sciences. 114
Mutations in 11β-hydroxysteroid dehydrogenase type 2 gene (HSD11B2) cause an extraordinarily rare autosomal recessive disorder, apparent mineralocorticoid excess (AME). AME is a form of low renin hypertension that is potentially fatal if untreated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7491d20b9585dd6eeb297474a26cd297
https://doi.org/10.1073/pnas.1716621115
https://doi.org/10.1073/pnas.1716621115
Autor:
Alireza Haghighi, Sian Ellard, Nancy Samir Elbarbary, Zahra Razavi, Matthew B. Johnson, Elisa De Franco, Aisha Al Senani, Sarah E. Flanagan, Z. Imane, Irfan Ullah, Saif Al-Yaarubi, Daphne Gardner, Zeynep Şıklar, Hana Lango Allen, Merih Berberoğlu, Andrew T. Hattersley
Publikováno v:
Diabetes
Young-onset autoimmune diabetes associated with additional autoimmunity usually reflects a polygenic predisposition, but rare cases result from monogenic autoimmunity. Diagnosing monogenic autoimmunity is crucial for patients’ prognosis and clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a0139e0942aa34509ab577f5e26c176
https://pubmed.ncbi.nlm.nih.gov/29305528
https://pubmed.ncbi.nlm.nih.gov/29305528
Autor:
Mabel, Yau, Hanan Said Al, Azkawi, Shozeb, Haider, Ahmed, Khattab, Maryam Al, Badi, Wafa, Abdullah, Aisha Al, Senani, Robert C, Wilson, Tony, Yuen, Mone, Zaidi, Maria I, New
Publikováno v:
Annals of the New York Academy of Sciences. 1376(1)
Apparent mineralocorticoid excess (AME) is a rare autosomal recessive genetic disorder causing severe hypertension in childhood due to a deficiency of 11β-hydroxysteroid dehydrogenase type 2 (11βHSD2), which is encoded by HSD11B2. Without treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c31fe99c1c5af1cdf9d3109fa1ea4772
https://pubmed.ncbi.nlm.nih.gov/27526338
https://pubmed.ncbi.nlm.nih.gov/27526338
Autor:
Zahra Razavi, Irfan Ullah, Saif Al-Yaarubi, Daphne Gardner, Aisha Al Senani, Z. Imane, Sarah E. Flanagan, Hana Lango Allen, Alireza Haghighi, Sian Ellard, Zeynep Şıklar, Nancy Samir Elbarbary, Matthew B. Johnson, Andrew T. Hattersley, Merih Berberoğlu, Elisa De Franco
Publikováno v:
Diabetes. 67:532.2-532
In the article listed above, Ayla Guven, of the Pediatric Endocrinology Clinic, Goztepe Educational and Research Hospital, Istanbul, …
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::537c0549189439397cc1e0250395f85f
https://doi.org/10.2337/db18-er03b
https://doi.org/10.2337/db18-er03b