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Journal of Nuclear Biology and Medicine (Turin, Italy : 1991)|October 1, 1991
Treatment of malignant pheochromocytoma with [131I]metaiodobenzylguanidine: a French multicenter studyM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1991
Use of m-[131I]iodobenzylguanidine in the treatment of malignant pheochromocytomaM Krempf, J Lumbroso, R Mornex, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinomaP Pigny, C Bauters, J L Wemeau, et al.
Clinical Endocrinology|March 12, 2008
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?C Cardot-Bauters, E Leteurtre, L Leclerc, et al.
Clinical Endocrinology|May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismM C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Annales De Chirurgie|March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]A Lamblin, P Pigny, G Tex, et al.
Clinical Lymphoma & Myeloma|April 14, 2009
Balancing risk versus benefit in the treatment of Waldenström's Macroglobulinemia patients with nucleoside analogue-based therapyXavier Leleu, Jérome Tamburini, Aldo Roccaro, et al.
European Journal of Medical Genetics|January 17, 2017
Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of "thyroid-checked" controlsBenjamin Kern, Lucie Coppin, Pauline Romanet, et al.
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