Results 51 to 60 of about 2,181,916 (247)

8479 A Challenging Case of Hypercortisolism in an Adult Patient With McCune Albright Syndrome [PDF]

J Endocr Soc
Disclosure: P. Kesavan Chary: None. S. Jasim: None. Background: McCune Albright Syndrome (MAS) is a rare genetic disorder that occurs due to a spontaneous post-zygotic missense mutation in the GNAS gene resulting in activating gain of function mutations ...
P. Chary, S. Jasim
europepmc   +2 more sources

Denosumab Reduces Lesional Fluoride Skeletal Burden on Na[18F]F PET-CT in Patients With Fibrous Dysplasia/McCune–Albright Syndrome

Journal of Clinical Endocrinology and Metabolism, 2021
Context The correlation between fibrous dysplasia/McCune–Albright syndrome (FD/MAS) skeletal disease burden on Na[18F]F positron emission tomography–computed tomography (PET-CT) and serum bone turnover markers (BTMs) was recently described. The effect of
W. van der Bruggen, D. Vriens, M. Meier, F. Smit, E. Winter, L. de Geus-Oei, N. Appelman‐Dijkstra   +6 more
semanticscholar   +1 more source

Hyperthyroidism related to McCune-Albright syndrome: report of two cases and review of the literature [PDF]

, 2008
INTRODUCTION: McCune-Albright syndrome is a sporadic disease clinicaly characterized by polyostotic fibrous dysplasia, café-au-lait cutaneous spots and hyperfunctional endocrinopathies, such as precocious puberty, hyperthyroidism, acromegaly and others ...
Abrahão, Márcio, Cervantes, Onivaldo, Leonhardt, Fernando Danelon, Sallum, Ana Carolina, Yazaki, Reinaldo Kazuo   +4 more
core   +2 more sources

A Rare Case of McCune-Albright Syndrome in Association with Acromegaly: Treatment Options and a Review of the Literature

Bagcilar Medical Bulletin, 2022
McCune-Albright syndrome constitutes of fibrous dysplasia, café-au-lait macules, and various endocrinopathies such as thyroid, cortisol, prolactin and growth hormone hypersecretion.
Hande Peynirci, Onur Elbasan
doaj   +1 more source

A multidisciplinary care pathway improves quality of life and reduces pain in patients with fibrous dysplasia/McCune-Albright syndrome: a multicenter prospective observational study

Orphanet Journal of Rare Diseases, 2022
Background Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) may cause pain, impaired ambulation and decreased quality of life (QoL). International guidelines advocate management of FD/MAS in a tertiary multidisciplinary care pathway, but no ...
M. Meier, M. Hagelstein-Rotman, A. C. van de Ven, I. V. D. van der Geest, Olav Donker, S. Pichardo, P. Hissink Muller, Stijn W van der Meeren, Desirée M J Dorleijn, E. Winter, M. V. D. van de Sande, N. Appelman‐Dijkstra   +11 more
semanticscholar   +1 more source

Clinical, microscopic and imaging findings associated to Mccune-Albright syndrome: report of two cases [PDF]

, 2008
McCune-Albright syndrome is characterized by the triad café-au-lait cutaneous spots, polyostotic fibrous dysplasia and endocrinopathies. This article presents two cases of McCune-Albright syndrome in a middle-aged woman and a young girl.
BRENTEGANI, Luiz Guilherme, LACERDA, Suzie Aparecida, RIBEIRO, Michel Campos, SICCHIERI, Luciana Gonçalves, XAVIER, Samuel Porfírio   +4 more
core   +1 more source

Soft Syndrome Decoding of Quantum LDPC Codes for Joint Correction of Data and Syndrome Errors [PDF]

arXiv, 2022
Quantum errors are primarily detected and corrected using the measurement of syndrome information which itself is an unreliable step in practical error correction implementations. Typically, such faulty or noisy syndrome measurements are modeled as a binary measurement outcome flipped with some probability.
arxiv  

Quantum Data-Syndrome Codes [PDF]

IEEE Journal on Selected Areas in Communications, vol. 38, no. 3, pp. 449-462, March 2020, 2019
Performing active quantum error correction to protect fragile quantum states highly depends on the correctness of error information--error syndromes. To obtain reliable error syndromes using imperfect physical circuits, we propose the idea of quantum data-syndrome (DS) codes that are capable of correcting both data qubits and syndrome bits errors.
arxiv   +1 more source

McCune-Albright-Braytsev syndrome: literature review and clinical case

Mìžnarodnij Endokrinologìčnij Žurnal, 2019
The paper presents the results of literature review on McCune-Albright-Braytsev syndrome and describes the clinical case of this syndrome. McCune-Albright-Braytsev syndrome is a genetically determined disease, usually chara­cterized by a triad of ...
T.V. Sorokman, O.V. Makarova, N.О. Popeliuk   +2 more
doaj   +1 more source

The Clinical Spectrum of McCune-Albright Syndrome and Its Management

Hormone Research in Paediatrics, 2019
McCune-Albright syndrome (MAS) is a rare, mosaic disorder presenting along a broad clinical spectrum. Disease arises from somatic-activating GNAS mutations, leading to constitutive Gαs activation and ligand-independent signaling of the Gαs-coupled ...
Tiahna A. Spencer, Kristen S. Pan, M. Collins, A. Boyce   +3 more
semanticscholar   +1 more source