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TITOLO AUTORI EDITORE ANNO DOSSIER PAGINE LINGUA
Identification of a mutation in the gene encoding the subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome Schwindinger WF, Francomano CA, Levine MA, Proc Natl Acad Sci USA 1992 89 5152-5156 en
Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome Cuttler L, Jackson JA, uz-Zafar MS, Levitsky L, Mellinger RC, Frohman LA, J Clin Endocrinol Metab 1989 68 1148-1154 en
Hypersecretion of growth hormone and prolactin in McCune-Albright syndrome Sultan C, Chevalier C, Leboucq N, Dumas R, Acta Paediatr Scand 1993 81 110 en
Hypercalemia in a child with Ewing's sarcoma and bisphosphonate therapy Sevinir BB, Akyuz C, Kotiloglu E, Hazar V, Buyjkpamukcu M, Turk J Cancer 1995 25 91-94 en
High concentrations of plasma immunoreactive inhibin during normal pregnancy in women Abe Y, Hasegawa Y, Miyamoto K, Yamaguti M, Andoh A, Ibuki Y, Igarashi M, J Clin Endocrinol Metab 1990 71 133-137 en
GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours Landis CA, Masters SB, Spada A, Pace AM, Bourne HR, Vallar L, Nature 1989 340 692-696 en
Gsα-related precocious puberty in Females: Focus on treatement T.S. Hannon Journal of Pediatric Endocrinology & Metabolism (JPEM) 2006 Volume 19, Suppl. 2 605-606 en
Gs alpha mutation at codon 201 in pituitary adenoma causing gigantism in a 6 year old boy with McCune-Albright syndrome Dotsch J, Kiess W, Hanze J, Repp R, Ludecke D, Blum WF, Rascher W, J Clin Endocrinol Metab 1996 81 3839-3842 en
Growth hormone-secreting pituitary adenoma associated with multiple bone cysts, skin pigmentation and aortitis syndrome Ihara C, Shimatsu H, Murabe K, Kataoka C, Kondo, Nakao K, J Endocrinol Invest 1996 19 753-757 en
Granulosa cell tumors of the ovary in children and adolescents. Multicenter retrospective study in 40 patients aged 7 months to 22 yeras Plantaz D, Flamant F, Vassal G, Chappuis JP, Baranzilli MC, Bouffet E, Dyon JF, Armari C, Bost M, Arch Fr Pediatr 1992 49 793-798 en
Gonadotropin independent precocious puberty Low LCK, Wang Q, Journal of Pediatric Endocrinology & Metabolism (JPEM) 1998 11 497-507 en
Glucorticoid-induced osteoporosis: pathogenesis and management Lukert BP, Raisz LG, Ann Intern Med 1990 112 352-364 en
Genetics of Pseudohypoparathyroidism types Ia and Ic M. A. Aldred Journal of Pediatric Endocrinology & Metabolism (JPEM) 2006 Volume 19, Suppl. 2 635-640 en
Genetics of McCune-Albright Syndrome L. de Sanctis, L. Delmastro, M.C. Russo, P. Matarazzo, R. Lala, C. de Sanctis Journal of Pediatric Endocrinology & Metabolism (JPEM) 2006 Volume 19, Suppl. 2 577-582 en
G proetin mutations in human disease Weinstein LS, Shenker A, Clin Biochem 1993 26 333-338 en
Functional and clinical consequences of mutations in the FSH receptor Gromoll J, Simoni M, Nordhoff V, Behre HM, De Geyter C, Nieschlag E, Mol Cell Endocrinol 1996 125 177-182 en
Fibrous dysplasia of the proximal part of the femur Guille JT, Kumar SJ, MacEwen D, J Bone Joint Surg 1998 80-A 648-658 en
Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation Riminucci M, Fisher LW, Shenker A, Spiegel AM, Bianco P, Robey PG, Am J Pathol 1997 151 1587-1600 en
Fibrous Dysplasia Stephenson RB, London MD, Hankin FM, Kaufer H, J Bone Joint Surg 1987 69-A 400-409 en
Fibrodysplasia ossificans. Presentation of a case of exceptional severity Cottafava F, Nieri S, Racugno A, Corciulo P, Prestandrea C, Brida di Prio S, Villa Venzano G, Pinelli G, Minerva Pediatr 1986 38 53-58 en
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