Mccune-Albright Syndrome Latest Advances

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.

Journal: Annales d'endocrinologie

Published: March 21, 2026

Effects of anti-RANKL, Zoledronate or combination therapy in a mouse model of fibrous dysplasia: a preclinical study.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: February 12, 2026

Genetics of Familial Acromegaly and Pituitary Gigantism.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 11, 2026

A Case of Pediatric Adrenocortical Carcinoma With McCune-Albright Syndrome Masquerading as Spontaneously Regressing Neuroblastoma.

Journal: Pediatric blood & cancer

Published: February 02, 2026

Biological Behavior of Craniofacial Fibrous Dysplasia in McCune-Albright Syndrome Compared With Nonsyndromic Disease.

Journal: The Journal of craniofacial surgery

Published: January 22, 2026

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

Journal: Kidney medicine

Published: January 09, 2026

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

Journal: Frontiers in endocrinology

Published: January 05, 2026

Skin lesions in patients treated with growth hormone and those with growth hormone excess: a current overview.

Journal: Frontiers in medicine

Published: December 29, 2025

Bilateral Lesions Are Linked to Postoperative Regrowth in Craniofacial Fibrous Dysplasia: Alkaline Phosphatase as a Marker of Clinical Phenotype.

Journal: Diagnostics (Basel, Switzerland)

Published: December 18, 2025

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

Journal: The Journal of clinical endocrinology and metabolism

Published: December 13, 2025

Intersecting Clues From Bone, Skin and Hormones: A Classical Presentation of Mc-cune Albright Syndrome.

Journal: QJM : monthly journal of the Association of Physicians

Published: December 08, 2025

Denosumab in pediatric patients with fibrous dysplasia/McCune-Albright syndrome: a single-center, open-labeled study.

Journal: Frontiers in endocrinology

Published: December 07, 2025

Mccune-Albright Syndrome Latest Advances

Find the Latest Research About Mccune-Albright Syndrome

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohort.

Effects of anti-RANKL, Zoledronate or combination therapy in a mouse model of fibrous dysplasia: a preclinical study.

Effects of anti-RANKL, Zoledronate or combination therapy in a mouse model of fibrous dysplasia: a preclinical study.

Genetics of Familial Acromegaly and Pituitary Gigantism.

Genetics of Familial Acromegaly and Pituitary Gigantism.

A Case of Pediatric Adrenocortical Carcinoma With McCune-Albright Syndrome Masquerading as Spontaneously Regressing Neuroblastoma.

A Case of Pediatric Adrenocortical Carcinoma With McCune-Albright Syndrome Masquerading as Spontaneously Regressing Neuroblastoma.

Biological Behavior of Craniofacial Fibrous Dysplasia in McCune-Albright Syndrome Compared With Nonsyndromic Disease.

Biological Behavior of Craniofacial Fibrous Dysplasia in McCune-Albright Syndrome Compared With Nonsyndromic Disease.

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report 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.

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

Skin lesions in patients treated with growth hormone and those with growth hormone excess: a current overview.

Skin lesions in patients treated with growth hormone and those with growth hormone excess: a current overview.

Bilateral Lesions Are Linked to Postoperative Regrowth in Craniofacial Fibrous Dysplasia: Alkaline Phosphatase as a Marker of Clinical Phenotype.

Bilateral Lesions Are Linked to Postoperative Regrowth in Craniofacial Fibrous Dysplasia: Alkaline Phosphatase as a Marker of Clinical Phenotype.

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

Intersecting Clues From Bone, Skin and Hormones: A Classical Presentation of Mc-cune Albright Syndrome.

Intersecting Clues From Bone, Skin and Hormones: A Classical Presentation of Mc-cune Albright Syndrome.

Denosumab in pediatric patients with fibrous dysplasia/McCune-Albright syndrome: a single-center, open-labeled study.

Denosumab in pediatric patients with fibrous dysplasia/McCune-Albright syndrome: a single-center, open-labeled study.