Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ashwini Maudhoo"'
Autor:
Ashwini Maudhoo, Avinaash Maharaj, Federica Buonocore, Gabriel Angel Martos-Moreno, Jesús Argente, John C Achermann, Li F Chan, Lou A Metherell
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Congenital isolated ACTH deficiency (IAD) is a rare condition characterised by low plasma ACTH and serum cortisol with normal production of other pituitary hormones. TBX19 (also known as TPIT) is a T-box pituitary restricted transcription factor impo
Externí odkaz:
https://doaj.org/article/0e7589f553444aaabd52e695b904977c
Autor:
Ashwini, Maudhoo, Asma, Khalil
Publikováno v:
Best Practice & Research Clinical Obstetrics & Gynaecology. 85:17-25
The COVID-19 pandemic has been at the forefront of medicine over the last few years. Pregnant women are often exposed to infectious agents that can be harmful not only to the mother but also to the foetus. Moreover, changes during pregnancy means tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::229f380434071ac8477af742fb58bee6
https://doi.org/10.1016/j.bpobgyn.2022.06.006
https://doi.org/10.1016/j.bpobgyn.2022.06.006
Autor:
Li F. Chan, Jesús Argente, Avinaash Maharaj, Gabriel Á. Martos-Moreno, Ashwini Maudhoo, Lou Metherell, Federica Buonocore, John C. Achermann
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Summary Congenital isolated ACTH deficiency (IAD) is a rare condition characterised by low plasma ACTH and serum cortisol with normal production of other pituitary hormones. TBX19 (also known as TPIT) is a T-box pituitary restricted transcription fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1139d17a27507a69590a7f7052aba3c0
http://europepmc.org/articles/PMC8495723
http://europepmc.org/articles/PMC8495723
Autor:
Dagan O Lonsdale, Joseph Salem, A. Draper, Victoria Taylor, Hannah Gardiner, Ashwin Sundaram, Emma Lombard, Anne Dunleavy, Natasha Benons, Jessica Gates, Ashwini Maudhoo, Yee-Ean Ong
Publikováno v:
Respiratory infections.
Introduction: COVID-19 arrived as a new disease entity to the UK in early 2020. As one of the tertiary hospitals to admit COVID-19 patients, we collected data in order to characterise patients Method: Data was collected on 771 patients admitted with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c6e92df9da76c7a3cc36bf057e8a2cb
https://doi.org/10.1183/13993003.congress-2020.3589
https://doi.org/10.1183/13993003.congress-2020.3589
Autor:
Li F. Chan, Ashwini Maudhoo, Lou Metherell, Federica Buonocore, Jesus Argente, John Achermann, Avinaash Maharaj, Gabriel A Martos-Moreno
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddf9b8631e5bd341dddbbfd70c456b0b
https://doi.org/10.1530/endoabs.59.cc2
https://doi.org/10.1530/endoabs.59.cc2
Autor:
Li F. Chan, Avinaash Maharaj, Louise A. Metherell, Ashwini Maudhoo, Leonardo Guasti, Tatiana V. Novoselova, Rathi Prasad
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 189
Hereditary adrenocorticotropin (ACTH) resistance syndromes encompass the genetically heterogeneous isolated or Familial Glucocorticoid Deficiency (FGD) and the distinct clinical entity known as Triple A syndrome. The molecular basis of adrenal resist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec6fbc6762920fa4d191d5b07c31f8ef
https://pubmed.ncbi.nlm.nih.gov/30817990
https://pubmed.ncbi.nlm.nih.gov/30817990
Autor:
Avinaash, Maharaj, Federica, Buonocore, Eirini, Meimaridou, Gerard, Ruiz-Babot, Leonardo, Guasti, Hwei-Ming, Peng, Cameron P, Capper, Neikelyn, Burgos-Tirado, Rathi, Prasad, Claire R, Hughes, Ashwini, Maudhoo, Elizabeth, Crowne, Timothy D, Cheetham, Caroline E, Brain, Jenifer P, Suntharalingham, Niccolò, Striglioni, Bilgin, Yuksel, Fatih, Gurbuz, Sangay, Gupta, Robert, Lindsay, Robert, Couch, Helen A, Spoudeas, Tulay, Guran, Stephanie, Johnson, Dallas J, Fowler, Louise S, Conwell, Aideen M, McInerney-Leo, Delphine, Drui, Bertrand, Cariou, Juan P, Lopez-Siguero, Mark, Harris, Emma L, Duncan, Peter C, Hindmarsh, Richard J, Auchus, Malcolm D, Donaldson, John C, Achermann, Louise A, Metherell
Publikováno v:
Journal of the Endocrine Society
Primary adrenal insufficiency (PAI) is a potentially life-threatening condition that can present with nonspecific features and can be difficult to diagnose. We undertook next generation sequencing in a cohort of children and young adults with PAI of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11fc5fb460c9f1cf492f16e2cea65bb8
https://pubmed.ncbi.nlm.nih.gov/30620006
https://pubmed.ncbi.nlm.nih.gov/30620006