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EAMAS - Associazione Europea amici della Sindrome di McCune-Albright

EAMAS - Associazione Europea amici della Sindrome di McCune-Albright

European Association Friends of Mc Cune Albright Syndrome

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Detrmination of Gsα protein activity in Albright's hereditary osteodystrophyW. Ahrens, O. HiortJournal of Pediatric Endocrinology & Metabolism (JPEM)2006Volume 19, Suppl. 2647-651en
Multihormonal resistance to Parathyroid Hormone, Thyroid Stimulating Hormone, and other normal and neurosensory stimuli in patients with PseudohypoparathyroidismJ-L W?İmeau, A-S Balavoine, M. Ladsous, F-L Velayoudom-Cephise, V. Vlaeminck-GuillemJournal of Pediatric Endocrinology & Metabolism (JPEM)2006Volume 19, Suppl. 2653-661en
Resitance to Growth Hormone Releasing Hormone and Gonadotropins in Albright's Hereditary OsteodystrophyG. Mantovani, A. SpadaJournal of Pediatric Endocrinology & Metabolism (JPEM)2006Volume 19, Suppl. 2663-670en
Albright's Hereditary OsteodystrophyL. C. WilsonJournal of Pediatric Endocrinology & Metabolism (JPEM)2006Volume 19, Suppl. 2671-673en
Pamidronate and calcitonin therapy of acute cancer-related hypercalcaemia in childrenSchmid I, Stachel D, Schon C, Bauer M, Haas RJ,Klin Padiat200121330-34en
Regression of bone lesions in Gaucher's disease during treatment with aminohydroxyproylidene bisphosphonate [Letter]Harinck HI, Bijvoet OL, van der Meer JW, Jones B, Onvlee GJ,Lancet1984ii513en
Long-term effects of intravenous pamidronate in fibrous dysplasia of boneLiens B, Delmas PD, Meunier PJ,Lancet1994343953-954en
Wirkung von Pamidronat auf Bescwerdebild und Knochenstoffwechsel bei fibroser Dysplasie und McCune-Albright-SyndromPfeilschifter J, Ziegler R,Med Klin199893352-359de
Use of pamidronate in the management of acute cancer-related hypercalcaemia in childrenYoung G, Shende A,Med Pediatr Oncol199830117-121en
Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophyRingel MD, Schwindinger WF, Levine MA,Medicine (Baltimore)199675171-184en
Fibrodysplasia ossificans. Presentation of a case of exceptional severityCottafava F, Nieri S, Racugno A, Corciulo P, Prestandrea C, Brida di Prio S, Villa Venzano G, Pinelli G,Minerva Pediatr19863853-58en
Activating and inactivating mutations in LH receptorsThemmen AP, Martens JW, Brunner HG,Mol Cell Endocrinol1998145137-142en
Functional and clinical consequences of mutations in the FSH receptorGromoll J, Simoni M, Nordhoff V, Behre HM, De Geyter C, Nieschlag E,Mol Cell Endocrinol1996125177-182en
An animal model of fibrous dysplasiaBianco P, Robey PG,Mol Med Today19995322-323en
Activating mutations of the stimulatory G protein in the McCune-Albright syndromeWeinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM,N Engl J Med19913251688-1695en
Treatment of precocious puberty in the McCune-Albright syndrome with the aromatase inhibitor testolactoneFeuillan PP, Foster CM, Pescovitz OH, Hench KD, Shawker T, Dwyer A, Malley JD, Barnes K, Loriaux DL, Cutler GB Jr,N Engl J Med19863151115-1119en
Failure of disodium etidronate in calcinosis due to dermatomyositis and sclerodermaMetzger AL, Singer FR, Bluestone R, Pearson CM,N Engl J Med19742911294-1296en
Cyclic administration of pamidronate in children with severe osteogenesis imperfectaGlorieux FH, Bishop NJ, Plotikin H, Chabot G, Lanoue G, Travers R,N Engl J Med1998339947-952en
Short-term effects of pamidronate in patients with Gaucher's disease and severe skeletal involvement [Letter]Ciani G, Cuttini M, Bembi B,N Engl J Med1997337712en
Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females. Report of five casesAlbright F, Butler AM, Hampton AO, Smith P,N Engl J Med1937216727-746en

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EAMAS - Associazione Europea amici della Sindrome di McCune-Albright
Via Borgovecchio, 25 - 10041 Carignano (TO) - Italy - Tel:+39 011-9697258 - Fax:+39 011-9697258