ISSN 1470-3947 (print) | ISSN 1479-6848 (online)

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Showing page 1 of results 1 - 10 of about 27 pages

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Accurate staging of non-alcoholic fatty liver disease through analysis of the urinary steroid metabolome
Ahmad Moolla; Amin; Beverly Hughes; Wiebke Arlt; Zaki Hassan-Smith; Lorna Gilligan; Matt Armstrong; Philip Newsome; Tahir Shah;
http://www.endocrine-abstracts.org/ea/0049/ea0049oc3.5.htm
Published: 2017-05-03

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Steroid metabolomics for accurate and rapid diagnosis of inborn steroidogenic disorders
Elizabeth Baranowski; Kerstin Bunte; Cedric H L Shackleton; Angela E Taylor; Beverley A Hughes; Michael Biehl; Peter Tino; Tulay
http://www.endocrine-abstracts.org/ea/0049/ea0049oc1.3.htm
Published: 2017-05-03

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Sleep Apneas in Silver Russell Syndrome: A Constant Finding
Eloise Giabicani; Michele Boule; Eva Galliani; Irene Netchine
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-458.htm
Published: 2015-08-26

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Steroid metabolomics for diagnosis of inborn steroidogenic disorders – bridging the gap between clinician and scientist through computational approaches
Elizabeth Baranowski; Kerstin Bunte; Cedric Shackleton; Angela Taylor; Beverley Hughes; Michael Biehl; Peter Tino; Tulay Guran;
http://www.endocrine-abstracts.org/ea/0044/ea0044p40.htm
Published: 2016-10-14

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The urinary steroid metabolome as a non-invasive tool to stage non-alcoholic fatty liver disease
Ahmad Moolla; Amin; Bev Hughes; Wiebke Arlt; Zaki Hassan-Smith; Matt Armstrong; Philip Newsome; Tahir Shah; Gaal Luc Van; An Ver
http://www.endocrine-abstracts.org/ea/0044/ea0044oc1.4.htm
Published: 2016-10-14

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Characterisation of parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) in 3 families with autosomal recessive hypoparathyroidism
Michael Bowl; Samantha Mirczuk; Lorraine Southam; Zulf Mughal; Fiona Ryan; Nick Shaw; Elaine Tham; Ze’ev Hochberg; Dov Tios
http://www.endocrine-abstracts.org/ea/0013/ea0013p126.htm
Published: 2007-03-01

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Characterisation of 25 calcium-sensing receptor mutations in disorders of calcium homeostasis
Paul Christie; Alan Curley; M Andrew Nesbit; Brian Harding; Michael Bowl; Rajesh Thakker
http://www.endocrine-abstracts.org/ea/0013/ea0013p1.htm
Published: 2007-03-01

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Mice deleted for a Multiple Endocrine Neoplasia Type 1 (MEN1) allele develop pancreatic, pituitary and parathyroid tumours in association with hypercalcaemia
Manuel Lemos; Brian Harding; Michael Bowl; Anita Reed; Hilda Tateossian; Tertius Hough; William Fraser; Michael Cheeseman; Rajes
http://www.endocrine-abstracts.org/ea/0013/ea0013oc22.htm
Published: 2007-03-01

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MicroRNAs, miR-15a and miR-16-1, are implicated in pituitary tumourigenesis via regulation of cyclin D1
Paul Newey; Rebecca Dyar; Andrew Nesbit; Mahsa Javid; Gerard Walls; Anita Reed; Michael Bowl; Rajesh Thakker
http://www.endocrine-abstracts.org/ea/0021/ea0021p305.htm
Published: 2010-03-31

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A novel dominant-negative Glial Cells Missing B (GCMB) mutation (Asn502His) is associated with autosomal dominant hypoparathyroidism and results in reduced transactivation activity
Michael Bowl; Samantha Mirzcuk; Carl Fratter; Treena Cranston; Jeremy Allgrove; Caroline Brain; Andrew Nesbit; Rajesh Thakker
http://www.endocrine-abstracts.org/ea/0021/ea0021p233.htm
Published: 2010-03-31

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