Zobrazeno 1 - 10
of 862
pro vyhledávání: '"familial diabetes mellitus"'
Autor:
Aashish Sethi, Nicola Foulds, Sarah Ehtisham, Syed Haris Ahmed, Jayne Houghton, Kevin Colclough, Mohammed Didi, Sarah E. Flanagan, Senthil Senniappan
Publikováno v:
JCRPE, Vol 12, Iss 4, Pp 420-426 (2020)
Mutations in the insulin receptor (INSR) gene are associated with insulin resistance and hyperglycaemia. Various autosomal dominant heterozygous INSR mutations leading to hyperinsulinemic hypoglycaemia (HH) have been described in adults and children
Externí odkaz:
https://doaj.org/article/465c2395160044719b053f7ff53ff2ba
Akademický článek
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Publikováno v:
Epidemiology and Health, Vol 45 (2023)
OBJECTIVES The aim of this study was to clarify the clinical trait of familial diabetes mellitus (DM) by analyzing participants’ risk of DM according to the age of DM onset in parents and siblings, and to evaluate individuals’ risk of DM-associat
Externí odkaz:
https://doaj.org/article/81e1705b22b94c049a94a3661d9d7a3b
Autor:
Sethi, Aashish1, Foulds, Nicola2, Ehtisham, Sarah3, Ahmed, Syed Haris4, Houghton, Jayne5, Colclough, Kevin5, Didi, Mohammed1, Flanagan, Sarah E.6, Senniappan, Senthil1 senthilkss@yahoo.co.uk
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. Dec2020, Vol. 12 Issue 4, p420-426. 7p.
Autor:
Sarah Ehtisham, Syed Haris Ahmed, Senthil Senniappan, Nicola Foulds, Sarah E. Flanagan, Jayne A L Houghton, Aashish Sethi, Mohammed Didi, Kevin Colclough
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 12, Iss 4, Pp 420-426 (2020)
JCRPE, Vol 12, Iss 4, Pp 420-426 (2020)
Mutations in the insulin receptor (INSR) gene are associated with insulin resistance and hyperglycaemia. Various autosomal dominant heterozygous INSR mutations leading to hyperinsulinemic hypoglycaemia (HH) have been described in adults and children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07982118faab2b02aa32eafca73d62e3
https://doi.org/10.4274/jcrpe.galenos.2019.2019.0106
https://doi.org/10.4274/jcrpe.galenos.2019.2019.0106
Autor:
Talat Saatov, Kha Karimov, Zafar Ibragimov, Timur Alimov, Nasiba Alimova, Anvar Abduvaliev, Kodirjon Boboev, Elvira Ibragimova, Tokhir Ishankhodjaev, Zulaykho Shamansurova, Abdunabi Tashtemirov
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::383943b61c4e14085b512f2af9418479
https://doi.org/10.1530/endoabs.81.ep331
https://doi.org/10.1530/endoabs.81.ep331
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Qureshi, Nadeem1 nadeem.qureshi@nottingham.ac.uk, Kai, Joe1 joe.kai@nottingham.ac.uk
Publikováno v:
BMC Health Services Research. 2008, Vol. 8, Special section p1-8. 8p. 4 Charts, 1 Graph.
Autor:
P Vasista, P Sundaram
Publikováno v:
BSPED.
Aim To understand the difference in presentation of an inherited condition depending on the mode of inheritance. Case Report Case A: 11 years old girl with history of tiredness, normal BMI, had high blood glucose BG (7.1 mmol/L) and HbA1c (45 mmol/mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a471815be27f4feafc747f6c7f35bc9
https://doi.org/10.1136/archdischild-2020-rcpch.375
https://doi.org/10.1136/archdischild-2020-rcpch.375
Autor:
Eleonora Morini, Ornella Ludovico, Diego Bailetti, Antonio Pizzuti, Marta Romani, Tommaso Mazza, Patinut Buranasupkajorn, Giorgio Basile, Massimo Carella, Antonella Marucci, Christine Mendonca, Vincenzo Trischitta, Timothy Hastings, Sabrina Prudente, Prapaporn Jungtrakoon, Federica Alberico, Elide Miccinilli, Fabrizio Barbetti, Alessandro Doria, Piero Marchetti, Stefano Pascarella, Luana Mercuri, Teresa Milano, Rosa Di Paola
Diabetes mellitus is a highly heterogeneous disorder encompassing several distinct forms with different clinical manifestations including a wide spectrum of age at onset. Despite many advances, the causal genetic defect remains unknown for many subty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59ada45139827a3e4e134d3db4d1c303
http://hdl.handle.net/11573/787433
http://hdl.handle.net/11573/787433
