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Showing page 1 of results 1 - 10 of about 20 matches for "maher-eamonn"

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SDH mutations in tumourigenesis
Eamonn Maher
http://www.endocrine-abstracts.org/ea/0050/ea0050s5.1.htm
Published: 2017-10-20

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Familial phaeochromocytoma syndromes
Eamonn Maher
http://www.endocrine-abstracts.org/ea/0013/ea0013s53.htm
Published: 2007-03-01

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Hypoxia-induced angiogenesis in pheochromocytoma
Eamonn Maher
http://www.endocrine-abstracts.org/ea/0020/ea0020s22.2.htm
Published: 2009-04-01

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Genetics and epidemiology of phaeochromocytoma/paraganglioma
Eamonn Maher
http://www.endocrine-abstracts.org/ea/0028/ea0028s10.1.htm
Published: 2012-03-01

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The role of in vivo metabolomics using H-MRS in SDH deficient disease
Ruth Casey; Mary McLean; Madhu Bassetti; Ben Challis; Helen Simpson; Mark Gurnell; Ramesh Bulusu; Alison Marker; Olivier Giger;
http://www.endocrine-abstracts.org/ea/0049/ea0049gp27.htm
Published: 2017-05-03

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A Nonsense Thyrotropin Receptor Gene Mutation (R609X) is Associated with Congenital Hypothyroidism and Heart Defects*
Hakan Cangul; Veysel Nijat Bas; Yaman Saglam; Michaela Kendall; Timothy G Barrett; Eamonn R Maher; Zehra Aycan
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d1-235.htm
Published: 2014-08-28

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Growth and Metabolic Phenotypes in Patients with SRS: a Multi-Centre Cross-Sectional Observational Study
Kayleigh Aston; Gemma Grosvenor; Catherine Peters; Verghese Mathew; Joanne Blair; Simon Chapman; Charles Buchanan; Eamonn Maher;
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-471.htm
Published: 2015-08-26

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Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B gene mutation carriers
Umasuthan Srirangalingam; Lisa Walker; Bernard Khoo; Fiona MacDonald; Daphne Gardner; Terence J Wilkin; Robert H Skelly; Emad Ge
http://www.endocrine-abstracts.org/ea/0015/ea0015oc1.htm
Published: 2008-04-01

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Phaeochromocytoma, paraganglioma and tumour genetics: clinical practice lagging theory?
Umasuthan Srirangalingam; Nirupa Sivathasan; Romaan Akhtar; Daniel Berney; Eamonn Maher; Shern Chew
http://www.endocrine-abstracts.org/ea/0025/ea0025p187.htm
Published: 2011-04-01

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A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism
Nadia Schoenmakers; Hakan Cangul; Adeline K Nicholas; Erik Schoenmakers; Greta Lyons; Mehul Dattani; Catherine Peters; Shirley L
http://www.endocrine-abstracts.org/ea/0033/ea0033oc2.9.htm
Published: 2013-11-01

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