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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
Osteodystrophia fibrosa: report of a cse in which the condition was combined with true precocious puberty, pathologic pigmentation of the skin, and hyperthyroidism, with a review of the literatureMc Cune DJ, Bruch H,Am J Dis Child193654806-848en
McCune-Albright syndrome associated with non-autoimmune type of hyperthyroidism with development of thyrotoxic crisisHaruhiko I, Sanda K, Kameoka K, Takamatsu J,Horn Res200053256-259en
Juvenile osteoporosis treated with pamidronateLevis S, Gruber HE, Cohn D, Howard GA, Roos BA,Calcified Tissue Int199352 (suppl)S41(Abst)en
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
Mutation screening and isoform prevalence of the follicle stimulating hromone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndromeConway GS, Conway E, Walker C, Hoppner W, Gromoll J, Simoni M,Clin Endocrinol (Oxf)19995197-99en
Osteogenesis imperfecta: a clinical study of the first ten years of lifeVetter U, Pontz B, Zauner E, Brenner RE, Spranger J,Calcified Tissue Int19925036-41en
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
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
An animal model of fibrous dysplasiaBianco P, Robey PG,Mol Med Today19995322-323en
Granulosa cell tumors of the ovary in children and adolescents. Multicenter retrospective study in 40 patients aged 7 months to 22 yerasPlantaz D, Flamant F, Vassal G, Chappuis JP, Baranzilli MC, Bouffet E, Dyon JF, Armari C, Bost M,Arch Fr Pediatr199249793-798en
Immunoreactivity of standard and reference preparation used in the radioimmunoassay of follicle-stimulating and luteinizing hormones in serumRosenberg E,J Clin Endocrinol Metab197948163-166en
Torsion of a functional ovarian cyst in a premenopausal patient receiving tamoxifenNasu K, Miyazaki T, Kiyonaga Y, Kawasaki J, Miyakawa I,Gynecol Obstet Invest199948200-202en
Case report: the ultrasound appearances of testicular micorlithiasis ('snow strom' testis): a case complicated by testicular seminomaRoberts IS, Loughran CF,Clin Radiol19934765-67en
The natural history of fibrous dysplasiaHarris WH, Dudley HR Jr, Barry RJ,J Bone Joint Surg196244-A207-233en
Direct measurement of TP/GFR: a simple and reliable parameter of renal phophate handlingStark H, Eisenstein B, Tieder M, Rachmel A, Alpert G,Nephron198644125-128en
Standards from birth to maturity for height, weight, heigt velocity, weight velocity: British children, 1965. Part II.Tanner JM, Whitehouse RH, Takhaishi M,Arch Dis Child196641613-635en
Monthly urinary gonadotropin and ovarian hormone execretory patterns in normal girls and female patients with idiopathic precocious pubertyMaesaka H, Tachibana K, Adachi M, Okada T,Pediatr Res199640853-860en
Bisphosphonates: pharmacology and effects on the growing skeletonPapapoulos SE,Acta Universitatis Carolinae Medica19944029-32en
Leukaemia-associated hypercalcaemia in a 10-yera-old boy: effectiveness of aminohydroxypropylidene biphosphonateBoudailliez BR, Pautard BJ, Sebert JL, Kremp O, Piussan CX,Pediatr Nephrol19904510-511en
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

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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