Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tarig Babiker"'
Autor:
Tarig Babiker, Siri Atma W. Greeley, Pamela Bowman, Sarah E. Flanagan, Jacques Beltrand, Fabrizio Barbetti, Janine Sanchez, Eamon Rawlins, Lisa R. Letourneau-Freiberg, Andrew T. Hattersley, Nicholas J. Thomas, Maggie Shepherd, Barbara Piccini, Michel Polak, Elisa De Franco, Sian Ellard, Frances Mathews
Publikováno v:
Diabetes Care. 44:35-42
OBJECTIVE ABCC8 mutations cause neonatal diabetes mellitus that can be transient (TNDM) or, less commonly, permanent (PNDM); ∼90% of individuals can be treated with oral sulfonylureas instead of insulin. Previous studies suggested that people with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56b8cfaf41ea2c9f63d3447fdaf8ca9b
https://doi.org/10.2337/dc20-1520
https://doi.org/10.2337/dc20-1520
Autor:
Rawlins E, De Franco E, Andrew T. Hattersley, Pamela Bowman, Barbara Piccini, Janine Sanchez, Greeley Saw, Tarig Babiker, Frances Mathews, Sarah E. Flanagan, Lisa R. Letourneau-Freiberg, Sian Ellard, Fabrizio Barbetti, Nicholas J. Thomas, M. Shepherd, Jacques Beltrand, Michel Polak
Publikováno v:
Yearbook of Paediatric Endocrinology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59974fcb57474aa6f2a5464c81bc0130
https://doi.org/10.1530/ey.18.2.8
https://doi.org/10.1530/ey.18.2.8
Autor:
the Neonatal Diabetes International Collaborative Group, Andrew T. Hattersley, Sarah E. Flanagan, Sian Ellard, Elisa De Franco, Nicholas J. Thomas, Tarig Babiker, Eamon Rawlins, Siri Atma W. Greeley, Michel Polak, Lisa R. Letourneau-Freiberg, Jacques Beltrand, Barbara Piccini, Janine Sanchez, Maggie H. Shepherd, Fabrizio Barbetti, Frances Mathews, Pamela Bowman
Objective ABCC8 mutations cause neonatal diabetes that can be transient (TNDM) or less commonly permanent (PNDM); ~90% individuals can be treated with oral sulfonylureas instead of insulin. Previous studies suggested that people with ABCC8-PNDM requi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d901acf511b46d4f3647d14539d33083
https://doi.org/10.2337/figshare.13053074.v1
https://doi.org/10.2337/figshare.13053074.v1
Autor:
Pamela, Bowman, Frances, Mathews, Fabrizio, Barbetti, Maggie H, Shepherd, Janine, Sanchez, Barbara, Piccini, Jacques, Beltrand, Lisa R, Letourneau-Freiberg, Michel, Polak, Siri Atma W, Greeley, Eamon, Rawlins, Tarig, Babiker, Nicholas J, Thomas, Elisa, De Franco, Sian, Ellard, Sarah E, Flanagan, Andrew T, Hattersley, Kara W, Greeley
Publikováno v:
Diabetes Care
OBJECTIVE: ABCC8 mutations cause neonatal diabetes that can be transient (TNDM) or less commonly permanent (PNDM); ~90% individuals can be treated with oral sulfonylureas instead of insulin. Previous studies suggested that people with ABCC8-PNDM requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30020173ea2a30277e4b57a65655eb0d
https://pubmed.ncbi.nlm.nih.gov/33184150
https://pubmed.ncbi.nlm.nih.gov/33184150
Autor:
Frances M. Ashcroft, Tarig Babiker, Roisin Finn, Sarah E. Flanagan, Maggie Shepherd, Andrew T. Hattersley, Natascia Vedovato, Nicholas J. Thomas, Sian Ellard, Ali J. Chakera, Roope Männikkö, Kashyap A. Patel
Publikováno v:
Diabetologia
Aims/hypothesis The finding that patients with diabetes due to potassium channel mutations can transfer from insulin to sulfonylureas has revolutionised the management of patients with permanent neonatal diabetes. The extent to which the in vitro cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64e9c5c14481acf68a28fc73bd69d1bb
https://doi.org/10.1007/s00125-016-3921-8
https://doi.org/10.1007/s00125-016-3921-8
Autor:
Simon Edeghere, Claire Morton, Sue Rogers, Tarig Babiker, Yamin Elzain, Antonia Brooke, Peninsula Endocrine Network
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::531065d81aa5cc02a051986d25e2c787
https://doi.org/10.1530/endoabs.59.p137
https://doi.org/10.1530/endoabs.59.p137
Autor:
Kashyap A, Patel, Bridget, Knight, Aftab, Aziz, Tarig, Babiker, Avades, Tamar, Joanna, Findlay, Sue, Cox, Ioannis, Dimitropoulos, Carolyn, Tysoe, Vijay, Panicker, Bijay, Vaidya
Publikováno v:
Clinical Endocrinology
Summary Objective Patients with hyperthyroidism lacking autoimmune features but showing diffuse uptake on thyroid scintigram can have either Graves’ disease or germline activating TSH receptor (TSHR) mutation. It is important to identify patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c2b3f894a37629f90f8486b93ad8b04
https://pubmed.ncbi.nlm.nih.gov/30372544
https://pubmed.ncbi.nlm.nih.gov/30372544
Autor:
Petur Benedikt Juliusson, Michel Polak, Åsta Sulen, Magdalena Szopa, Ethel Codner, Nicholas J. Thomas, Tessmann Eh, Torild Skrivarhaug, Jacques Beltrand, Pamela Bowman, Iwar Klimes, Pernille Svalastoga, M. Shepherd, Fabrizio Barbetti, Ewan R. Pearson, Pål R. Njølstad, Sian Ellard, Dario Iafusco, Tarig Babiker, Sarah E. Flanagan, Andrew T. Hattersley
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbf7247b90574b00a91bec6490c551c8
http://hdl.handle.net/2108/208514
http://hdl.handle.net/2108/208514
Autor:
Antonia Brooke, Efstathia Kyrodimou, Mark Gurnell, Tarig Babiker, Daniel M. Berney, William Drake
Publikováno v:
Clinical Case Reports
Key Clinical Message A 60‐year‐old man with a pre‐existing stable sacrococcygeal teratoma developed acromegaly, ectopic Cushing's syndrome, and 5HIAA secretion. To our knowledge, this represents the first reported case of ACTH and serotonin sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0819dd95ae4d2c0cacfedcfdf020a7d6
https://www.repository.cam.ac.uk/handle/1810/285035
https://www.repository.cam.ac.uk/handle/1810/285035
Autor:
Timothy J. McDonald, Bridget A. Knight, Rachel Besser, Maggie Shepherd, Tarig Babiker, Sarah E. Flanagan, Mandy H Perry, Sian Ellard, Andrew T. Hattersley
Publikováno v:
Diabetologia
Aims/hypothesis The majority of infants with neonatal diabetes mellitus present with severe ketoacidosis at a median of 6 weeks. The treatment is very challenging and can result in severe neurological sequelae or death. The genetic defects that cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc52f203048e7630bdcbd04ffb0d219b
https://pubmed.ncbi.nlm.nih.gov/28779213
https://pubmed.ncbi.nlm.nih.gov/28779213