Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Oliver Clifford-Mobley"'
Autor:
Oliver Clifford-Mobley, Jaime Matthews
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 60:219-220
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 57:69-76
Background Measurement of serum neuron-specific enolase (NSE) for neuro-prognostication post out-of-hospital cardiac arrest (OHCA) is recommended by international guidelines. There is, however, a lack of consensus regarding the cut-offs and time poin
Autor:
Oliver Clifford-Mobley, Kieron Rooney
Publikováno v:
Resuscitation. 168
Autor:
Jenifer P. Suntharalingham, Ignacio del Valle, John C. Achermann, Gerard S. Conway, Elim Man, Niccolo Striglioni, Gill Rumsby, Federica Buonocore, Lin Lin, Thomas F J King, Oliver Clifford-Mobley, Carlos F. Lagos
Publikováno v:
Journal of the Endocrine Society
Context The genetic basis of human sex development is slowly being elucidated, and >40 different genetic causes of differences (or disorders) of sex development (DSDs) have now been reported. However, reaching a specific diagnosis using traditional a
Autor:
Sam Sheerin, Oliver Clifford-Mobley
Publikováno v:
Annals of clinical biochemistry. 58(4)
Autor:
Oliver Clifford-Mobley
Publikováno v:
Annals of clinical biochemistry. 58(2)
Autor:
Swati Kanodia, Gill Rumsby, Oliver Clifford-Mobley, Mohammed Didi, Richard Holt, Senthil Senniappan
Publikováno v:
Pediatric Nephrology. 32:2159-2163
A baby girl was born at 39 weeks gestation to consanguineous Asian parents. From day 1 of life she had severe hypoglycaemia with an inappropriately elevated insulin concentration consistent with congenital hyperinsulinism (CHI), confirmed by the find
Publikováno v:
Urolithiasis. 44:333-337
Hyperoxaluria is a well-recognised risk factor for urolithiasis and patients with primary hyperoxaluria (PH) gradually build up calcium oxalate deposits leading to chronic kidney disease. Efforts to improve treatment for PH have focused on reducing u
Autor:
Oliver Clifford-Mobley, Francis Lam
Publikováno v:
Disorders of Steroidogenesis ISBN: 9783319963631
The phenotype of some inborn errors of cholesterol biosynthesis may present with symptoms suggestive of adrenal or gonadal steroid disorders. An overview of cholesterol biosynthesis is presented with more in-depth coverage of two disorders in which a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::348abed70b4a65cdd247af8a4fd99cab
https://doi.org/10.1007/978-3-319-96364-8_14
https://doi.org/10.1007/978-3-319-96364-8_14
Autor:
Oliver Clifford-Mobley
Publikováno v:
Disorders of Steroidogenesis ISBN: 9783319963631
Aldosterone synthase deficiency is an inborn error of metabolism that selectively impairs renal retention of salt and fluid. Clinically the disorder can present with a salt-losing crisis in infancy. Patients surviving this period may be asymptomatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da6334ad68ff6dc5eb6194076a33daf
https://doi.org/10.1007/978-3-319-96364-8_9
https://doi.org/10.1007/978-3-319-96364-8_9