Results 201 to 210 of about 6,163 (220)
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Trends in Endocrinology & Metabolism, 1993
McCune-Albright syndrome (MAS) is characterized by the clinical triad of polyostotic fibrous dysplasia, cafe-au-lait pigmented skin lesions, and multiple endocrinopathies. The molecular basis of MAS is a mutation in G(s)alpha that results in constitutive activation of adenylyl cyclase in affected tissues. This mutation occurs during early embryogenesis,
W F, Schwindinger, M A, Levine
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McCune-Albright syndrome (MAS) is characterized by the clinical triad of polyostotic fibrous dysplasia, cafe-au-lait pigmented skin lesions, and multiple endocrinopathies. The molecular basis of MAS is a mutation in G(s)alpha that results in constitutive activation of adenylyl cyclase in affected tissues. This mutation occurs during early embryogenesis,
W F, Schwindinger, M A, Levine
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Infantile McCune–Albright Syndrome
Pediatric Dermatology, 2001McCune–Albright syndrome is a rare disorder caused by an activating mutation of the α subunit of the Gs protein and is characterized by multiple hormonal abnormalities, fibrous dysplasia of bone, and cutaneous pigmentation. We report a 10‐week‐old infant with McCune–Albright syndrome. He presented with failure to thrive, cardiorespiratory distress, and
Davies, J.H. +3 more
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Acta Endocrinologica, 1986
Abstract. The presence of polyostotic fibrous dysplasia of bone, hyperpigmented skin macules, and precocious sexual development in children is known as the McCune-Albright syndrome. To date, a complex combination of multiple endocrinopathies including goiter, hyperthyroidism, acromegaly, Cushing syndrome, hyperprolactenemia, sexual precocity ...
N, Mauras, R M, Blizzard
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Abstract. The presence of polyostotic fibrous dysplasia of bone, hyperpigmented skin macules, and precocious sexual development in children is known as the McCune-Albright syndrome. To date, a complex combination of multiple endocrinopathies including goiter, hyperthyroidism, acromegaly, Cushing syndrome, hyperprolactenemia, sexual precocity ...
N, Mauras, R M, Blizzard
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McCune-Albright Syndrome with Acromegaly
Hormone and Metabolic Research, 1989This article demonstrates that acromegaly and hyperprolactinaemia can occur in a patient with McCune-Albright syndrome without any evidence of other endocrine ...
Chan, G +5 more
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1987
The McCune Albright syndrome is characterized in complete form by (a) patchy areas of a particular type of progressive bone disease termed polyostotic fibrous dysplasia; (b) multiple areas of cutaneous light brown pigmentation or cafe au lait spots; and (c) autonomous hyperfunction of one or more of the endocrine system, especially the gonads and ...
M, Danon, J D, Crawford
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The McCune Albright syndrome is characterized in complete form by (a) patchy areas of a particular type of progressive bone disease termed polyostotic fibrous dysplasia; (b) multiple areas of cutaneous light brown pigmentation or cafe au lait spots; and (c) autonomous hyperfunction of one or more of the endocrine system, especially the gonads and ...
M, Danon, J D, Crawford
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JAMA, 1986
This article describes clinical follow-up of 15 patients—13 females and two males—with McCune-Albright syndrome. Osseous fractures occurred only during childhood, while hearing impairment due to temporal bone involvement occurred in four of six adults.
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This article describes clinical follow-up of 15 patients—13 females and two males—with McCune-Albright syndrome. Osseous fractures occurred only during childhood, while hearing impairment due to temporal bone involvement occurred in four of six adults.
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McCune-Albright Syndrome with Thyrotoxicosis
Clinical Nuclear Medicine, 2001The authors report a rare case of McCune-Albright syndrome in a 5-year-old boy with thyrotoxicosis resulting from a hyperfunctioning solitary thyroid nodule shown on a Tc-99 thyroid scan. He also had an associated elevated parathyroid hormone level. Since 1963, only 34 cases of McCune-Albright syndrome with hyperthyroidism have been described.
A K, Singh +4 more
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Journal of Pediatric Endocrinology and Metabolism, 2007
Alan, Daneman, Denis, Daneman
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Alan, Daneman, Denis, Daneman
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