Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Oluwakemi Lokulo‐Sodipe"'
Autor:
Oluwakemi Lokulo‐Sodipe, Eloïse Giabicani, Ana P. M. Canton, Nawfel Ferrand, Jenny Child, Emma L. Wakeling, Gerhard Binder, Irène Netchine, Deborah J. G. Mackay, Hazel M. Inskip, Christopher D. Byrne, I. Karen Temple, Justin H. Davies
Publikováno v:
Clinical Endocrinology. 97:284-292
Objective: Silver–Russell syndrome (SRS) causes short stature. Growth hormone (GH) treatment aims to increase adult height. However, data are limited on the long-term outcomes of GH in patients with molecularly confirmed SRS. This study evaluated h
Publikováno v:
Paediatrics and Child Health. 32:31-36
Diabetes mellitus is a common long-term childhood condition, which paediatricians, allied healthcare professionals and paediatric trainees will encounter frequently. General or acute paediatric trainees will be involved in treatment initiation, reque
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Paediatrics and Child Health. 31:330-334
Excessive thirst is termed polydipsia and this is usually accompanied by excessive drinking and an increased urine output. Polyuria is the passage of unusually large volumes of dilute, pale urine. Diabetes mellitus is an important cause, which should
Autor:
Hazel Inskip, Jenny Child, Christopher D. Byrne, Angela Fenwick, Deborah J G Mackay, Elizabeth Jenkinson, I. Karen Temple, Lisa Marie Ballard, Emma Wakeling, Oluwakemi Lokulo-Sodipe, Justin H Davies
Publikováno v:
Archives of Disease in Childhood. 106:1195-1201
ObjectiveThe psychosocial impact of growing up with Silver-Russell syndrome (SRS), characterised by growth failure and short stature in adulthood, has been explored in adults; however, there are no accounts of contemporary lived experience in adolesc
Autor:
Zeshan Qureshi, Alexandra Richards, Camilla C Kingdon, Ian Sinha, Oluwakemi Lokulo-Sodipe, Anna M Rose
Publikováno v:
Archives of disease in childhood.
Autor:
Oluwakemi Lokulo-Sodipe, Hazel. M. Inskip, Christopher D. Byrne, Jenny Child, Emma L. Wakeling, Deborah J.G. Mackay, I. Karen Temple, Justin H. Davies
Publikováno v:
Endocrine Abstracts.
Autor:
Emma Wakeling, Jenny Child, Deborah J G Mackay, Miho Ishida, Christopher D. Byrne, Justin H Davies, I. Karen Temple, Oluwakemi Lokulo-Sodipe, Hazel Inskip, Gudrun E. Moore, Angela Fenwick, Lisa Marie Ballard
Publikováno v:
Journal of Medical Genetics
BackgroundSilver-Russell syndrome is an imprinting disorder that restricts growth, resulting in short adult stature that may be ameliorated by treatment. Approximately 50% of patients have loss of methylation of the imprinting control region (H19/IGF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fcf40152ba1c5a1d9381d94b71adf0
https://eprints.soton.ac.uk/437350/
https://eprints.soton.ac.uk/437350/
Autor:
I. Karen Temple, Deborah J G Mackay, Lisa Marie Ballard, Jenny Child, Angela Fenwick, Emma Wakeling, Justin H Davies, Hazel Inskip, Christopher D. Byrne, Elizabeth Jenkinson, Oluwakemi Lokulo-Sodipe
Publikováno v:
Archives of Disease in Childhood. 104:76-82
ObjectiveThere is limited information on the psychosocial impact of growing up with Silver-Russell syndrome (SRS), characterised by slow growth in utero leading to short stature in adulthood. Such information could aid families in making difficult tr
Autor:
I. Karen Temple, Deborah J G Mackay, Justin H Davies, Andrew Dauber, Oluwakemi Lokulo-Sodipe, Diana S Brightman, Beverly A Searle
Publikováno v:
Hormone Research in Paediatrics. 90:407-413
Background/Aims: Temple syndrome is an imprinting disorder caused by maternal uniparental disomy of chromosome 14 (mat UPD14), paternal deletion of 14q32 or paternal hypomethylation of the intergenic differentially methylated region (MEG3/DLK1 IG-DMR