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Results for
""Fibrous Dysplasia, Polyostotic""[mesh_terms]

13 Results

Searching titles within these results

Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting.

A Simon, H P Koppeschaar, J F Roijers, J W Höppener, C J Lips

The Netherlands journal of medicine 2000;56(3):100-9

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Safety of therapy with and withdrawal from denosumab in fibrous dysplasia and McCune-Albright syndrome: an observational study.

Maartje E Meier, Stance N Clerkx, Elizabeth M Winter, Alberto M Pereira, Annenienke C van de Ven, Michiel A J van de Sande, Natasha M Appelman-Dijkstra

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2021;36(9):1729-1738

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Clinical approach to clarifying the mechanism of abnormal bone metabolism in McCune-Albright syndrome.

Takehisa Yamamoto

Journal of bone and mineral metabolism 2006;24(1):7-10

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Head and neck manifestations of an undiagnosed McCune-Albright syndrome: clinicopathological description and literature review.

Mariana Gomes, Beatriz Lecumberri, José Juan Pozo-Kreilinger, Isabel Esteban, Aránzazu Royo, Álvaro Gómez de la Riva, Guiomar Pérez de Nanclares

Virchows Archiv : an international journal of pathology 2018;473(5):645-648

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Case Report: A case of x-linked hypophosphatemic rickets complicated with polyostotic fibrous dysplasia caused by PHEX gene mutation and literature review.

Shuijin Huang, Anhua Lin, Na Zhang, Wenjing He, Yanan Huo, Chenxiu Wang

Frontiers in endocrinology 2026;17():1781382

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Fibrous dysplasia, phosphate wasting and fibroblast growth factor 23.

Erik A Imel, Michael J Econs

Pediatric endocrinology reviews : PER 2007;4 Suppl 4():434-9

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The journey from vitamin D-resistant rickets to the regulation of renal phosphate transport.

Barton S Levine, Charles R Kleeman, Arnold J Felsenfeld

Clinical journal of the American Society of Nephrology : CJASN 2010;4(11):1866-77

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Activating and inactivating mutations in the human GNAS1 gene.

M A Aldred, R C Trembath

Human mutation 2000;16(3):183-9

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Tamoxifen improved final height prediction in a girl with McCune-Albright syndrome: patient report and literature review.

Pairunyar Sawathiparnich, Prapanrat Osuwanaratana, Jeerunda Santiprabhob, Supawadee Likitmaskul

Journal of pediatric endocrinology & metabolism : JPEM 2006;19(1):81-6

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G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.

Lee S Weinstein

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2007;21 Suppl 2():P120-4

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Impact of endocrine hyperfunction and phosphate wasting on bone in McCune-Albright syndrome.

R Lala, P Matarazzo, M Andreo, C Defilippi, C de Sanctis

Journal of pediatric endocrinology & metabolism : JPEM 2003;15 Suppl 3():913-20

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Fibrous dysplasia of bone and McCune-Albright syndrome.

Roland D Chapurlat, Philippe Orcel

Best practice & research. Clinical rheumatology 2008;22(1):55-69

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Genetic and hereditary aspects of childhood obesity.

I Sadaf Farooqi

Best practice & research. Clinical endocrinology & metabolism 2005;19(3):359-74

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Results: 1 – 13 / 13

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Results for ""Fibrous Dysplasia, Polyostotic""[mesh_terms]

Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting.

Safety of therapy with and withdrawal from denosumab in fibrous dysplasia and McCune-Albright syndrome: an observational study.

Clinical approach to clarifying the mechanism of abnormal bone metabolism in McCune-Albright syndrome.

Head and neck manifestations of an undiagnosed McCune-Albright syndrome: clinicopathological description and literature review.

Case Report: A case of x-linked hypophosphatemic rickets complicated with polyostotic fibrous dysplasia caused by PHEX gene mutation and literature review.

Fibrous dysplasia, phosphate wasting and fibroblast growth factor 23.

The journey from vitamin D-resistant rickets to the regulation of renal phosphate transport.

Activating and inactivating mutations in the human GNAS1 gene.

Tamoxifen improved final height prediction in a girl with McCune-Albright syndrome: patient report and literature review.

G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.

Impact of endocrine hyperfunction and phosphate wasting on bone in McCune-Albright syndrome.

Fibrous dysplasia of bone and McCune-Albright syndrome.

Genetic and hereditary aspects of childhood obesity.

Results for
""Fibrous Dysplasia, Polyostotic""[mesh_terms]