Výsledky vyhledávání - "Helen Eisenhauer"

Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions

Autor: Helen Eisenhauer, Tjitske Kleefstra, Marjolein H. Willemsen, Annemarie Ferwerda, Hanneke Rensen, Morag N. Collinson, John C. K. Barber, Ivan F M Lo, Stephen T.S. Lam, Nicole de Leeuw, Joanne Morris, Catherine L. Mercer, Ben C.J. Hamel

Publikováno v: American Journal of Medical Genetics Part A. 155:106-112

Deletions of the distal 3q22.3 region encompassing the gene forkhead transcription factor FOXL2 (FOXL2) usually result in intellectual disability (ID) and the highly recognizable blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). We encount

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef7bc788495f190b8b2174222a90b100
https://doi.org/10.1002/ajmg.a.33715

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Safer fluid prescribing at North Bristol Trust: Bringing practice in line with NICE Guidance with a redesign of the fluid prescription chart

Autor: Johanna Andersson, Thomas Bull, Daniel Paul, Emily Reynolds, Aimi Nishimura, Jessica Lloyd, Amanda Jetley, Mari Davies, Helen Eisenhauer, Daniel Maggs, Sorcha Clapham, Kaushali Trivedi, Robert Hair, Benjamin Plumb

Publikováno v: BMJ Quality Improvement Reports

The National Institute of Clinical Excellence (NICE) released new fluid guidelines following data suggesting 20% of patients receiving fluids suffer adversely (2013). This quality improvement group assessed fluid prescribing in a tertiary teaching ce

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f17e06f78bb19212d4ac0aa226fcd7c2
https://pubmed.ncbi.nlm.nih.gov/26734333

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