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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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Pubblicazioni

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PATOLOGIA: LINGUA:  
ARGOMENTO: TESTO:
TITOLOAUTORIEDITOREANNODOSSIERPAGINELINGUA
A case of pituitary adenoma associated with McCune-Albright syndromeSakaki S, Yokoyama S, Mamitsuka K, Nakayama M, Goto M, Kuratsu J,Pituitary19991297-302en
A follicular cyst during tamoxifen therapy in premenopausal breast cancer womanTerada S, Uchide K, Suzuki N, Akasofu K,Gynecol Obstet Invest19933562-64en
A mutation in the follicle-stimulating hormone receptor occurs frequently in human ovarian sex cord tumorsKotlar TJ, Young RH, Albanese C, Crowley WF Jr, Scully RE, Jameson JL,J Clin Endocrinol Metab1997821020-1026en
A new constitutively activating mutation of the G, protein alpha subunit-gsp oncogene is found in human pituitary tumoursClementi E, Malgaretti N, Meldolesi J, Taramelli R,Oncogene199051059-1061en
A novel GNASI mutation, R201G, in McCune-Albright syndromeRiminucci M, Fisher LW, Majolagbe A, Corsi A, Lala R, De Sanctis C, Robey PG, Bianco P,J Bone Miner Res1999141987-1989en
Abnormalities in G-protein-coupled signal transduction pathways in human diseaseSpiegel AM, Weinstein LS, Shenker A,J Clin Invest1993921119-1125en
Absence of pubertal gonadotropin secretion in girls with McCune-Albright syndromeFoster CM, Ross Jl, Shawker T, Pescovitz OH, Loriaux DL, Cutler GB Jr,J Clin Endocrinol Metab198451161-1165en
Acromegaly and its treatment in the McCune-Albright syndromePremawardhana LDKE, Vora JP, Mills R, Scanalon MF,Clin Endocrinol199236605-608en
Activating and inactivating mutations in LH receptorsThemmen AP, Martens JW, Brunner HG,Mol Cell Endocrinol1998145137-142en
Activating mutation of Gs alpha in McCune-Albright syndrome causes skin pigmentation by tyrosinase gene activation on affected melanocytesKim IS, Kim ER, Nam HJ, Chin MO, Moon YH, Oh MR, Yeo UC, Song SM, Kim JS, Uhm MR, Beck NS, Jin DkHorm Res199952235-240en
Activating mutation of the stimulatory G protein (gsp) as a putative cause of ovarian and testicular human stromal Leydig cell tumorsFragoso MC, Latronico AC, Carvalho FM, Zerbini MC, Marcondes JA, Araujo LM, Lando VS , Frazzatto ET, Mendonca BB, Villares SM,J Clin Endocrinol Metab1998832074-2078en
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
Albright's Hereditary OsteodystrophyL. C. WilsonJournal of Pediatric Endocrinology & Metabolism (JPEM)2006Volume 19, Suppl. 2671-673en
Altered Gs and adenylate cyclase activity in human GH-secreting pituitary adenomasVallar L, Spada A, Giannattasio G,Nature1987330566-567en
Aminohydroxy propylidene bisphosphonate (APD) treatment improves the clinical skeletal manifestaions of Gaucher's dieseaseSamuel R, Katz K, Papapoulos SE, Yosipovitch Z, Zaizov R, Liberman U,Pediatrics199494385-389en
Aminohydroxy-propylidene bisphosphonate (AHPrBP) treatment of severe immobilization hypercalcaemia in a young patientVarache N, Audran M, Clochon P, Lortholary A, Bouachour G, Alquier P, Basle MF,Clin Rheumatol199110328-332en
Aminohydroxypropylidene-bisphosphonate in the treatment of bone lesions in a case of Gaucher's disease type 3Bembi B, Agosti E, Boehm P, Nassimbeni G, Zanatta M, Vidoni L,Acta Paediatr Scand199483122-124en
An activating Gsa mutation in present in fibrous dyspalsia of bone in the McCune-Albright syndromeShenker A, Weinstein LS, Sweet DE, Spiegel AM,J Clin Endocrinol Metab199479750-755en
An animal model of fibrous dysplasiaBianco P, Robey PG,Mol Med Today19995322-323en
An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesionMalchoff CD, Reardon G, MacGillivary DC, Yanase H, Rogol AD, Malchoff DM,J Clin Endocrinol Metab199478803-806en

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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