Endocrine manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic imprinting
Weinstein Ls, Yu S, Warner DR, Liu J,
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2001
22
675-705
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The stimulatory G protein alpha-subunit gene: mutations and imprintig lead to complex phenotypes
Weinstein Ls,
J Clin Endocrinol Metab
2001
86
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Dynamics of ovarian function in an adult woman with McCune-Albright syndrome
Laven JS, Lumbroso S, Sultan C, Fauser BC,
J Clin Endocrinol Metab
2001
86
2625-2630
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Dynamics of ovarian function in an adult woman with McCune-Albright syndrome
Laven JSE, Lumbroso S, Sultan C, Fauser SCJM,
J Clin Endocrinol Metab
2001
86
2625-2630
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Stress and the reproductive cycles
Ferin M,
J Clin Endocrinol Metab
2001
84
1768-1774
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Early fractures and occult hyperthyroidism: McCune-Albright syndrome?
Di Candia S, Weber G, Mora S, de Pellegrin M, Chiumello G,
Horn Res
2001
56
56-58
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Renal phosphate wasting in fibrous dysplasia of bone is a part of generalized renal tubular dysfunction similar to that seen in tumor-induced osteomalacia
Collins Mt, Chebil C, Jones J, Kushner H, Consugar M, Rinaldo P, Wientroub S, Bianco P, Robey PG,
J Bone Miner Res
2001
16
806-813
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Sonographic testicular microlithiasis as indicator of premalignant conditions in normal and infertile men
Von Eckardstein S, Tsakmakidis G, Kamischke A, Rolf C, Nieschlag E,
J Androl
2001
285
818-824
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Macroorchidism due to autonomous hyperfuncion of Sertoli cells and g(s)alpha gene mutation: an unusual expression of McCune-Albright syndrome in a prepubertal boy
Coutant R, Lumbroso S, Rey R, Lahlou N, Venara M, Rouleau S, Sultan C, Limal JM,
J Clin Endocrinol Metab
2001
86
1778-1781
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Pamidronate and calcitonin therapy of acute cancer-related hypercalcaemia in children
Schmid I, Stachel D, Schon C, Bauer M, Haas RJ,
Klin Padiat
2001
213
30-34
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Armidex Writing Committee; Investigators Committee Members. Anastrozole is superior to tamoxifen as first-line therapy in hormone receptor positive advanced breast carcinoma
Bonneterre J, Buzard A, Nabholtz JM, Robertson JF, Thurlimann B, von Euler M, Sahmoud T, Webster A, Steinberg M,
Cancer
2001
92
2247-2258
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Demonstration of McCune-Albright mutations in the liver of children whit hig Ygt progressive cholestasis
Silva ES, Lumbroso S, Medina M, Gillerot Y, Sultan C, Sokal EM,
J Hepatol
2000
32
154-158
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Mutations of the GNASI gene, stromal cell dysfunction, and osteomalacic changes in non McCune-Albright fibrous dysplasia of bone
Bianco P, Riminucci M, Majolagbe A, Kuznetsov SA, Collins MT, Mankani MH, Corsi A, Bone HG, Wientroub S, Spiegel AM, Fisher LW , Gheron Robey P
J Bone Min Res
2000
15
120-125
en
Characterization of autonomous thyroid adenoma: metabolism, gene expression, and pathology
Deleu S, Allory Y, Radulescu A, Pirson I, Carrasco N, Corvilain B, Salmon I, Franc B, Dumont JE, Van Sande J, Maenhaut C,
Thyroid
2000
10
131-140
en
The human thyrotropin receptor is highly mutable: a review of gain-of-function mutation
Farid NR, Kascur V, Balazs C,
Eur J Endocrinol
2000
143
25-30
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The extracellular domain suppresses constitutive activity of the transmembrane domain of the human TSH receptor: implications for hormone-receptor interaction and antagonist design
Mutation analysis of the follicle-stimulating hormone receptor gene in girls with gonadotropin-indipendent precocious puberty resulting from autonomous cystic ovaries
