Výsledky vyhledávání - "Marilyn H. Kelly"

Transient Increased Calcium and Calcitriol Requirements After Discontinuation of Human Synthetic Parathyroid Hormone 1-34 (hPTH 1-34) Replacement Therapy in Hypoparathyroidism

Autor: Beth A Brillante, Lori C. Guthrie, Marilyn H. Kelly, Rachel I Gafni, Robert James, Nancy A Yovetich, Michael T. Collins, James C. Reynolds, C Michele Christie

Publikováno v: Journal of Bone and Mineral Research. 30:2112-2118

Synthetic human PTH 1-34 (hPTH 1-34) replacement therapy in hypoparathyroidism maintains eucalcemia and converts quiescent bone to high-turnover bone. However, the skeletal and metabolic effects of drug discontinuation have not been reported. Nine su

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::26190996ccfca249d1a3d35219d3a89a
https://doi.org/10.1002/jbmr.2555

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Tumor localization and biochemical response to cure in tumor-induced osteomalacia

Autor: Gad B Kletter, Richard M. Sherry, Diana Ovejero Crespo, Clara C. Chen, Alison M. Boyce, Lori C. Guthrie, Andrew J. Dwyer, William H. Chong, Richard Chang, Diala El-Maouche, Felasfa M. Wodajo, James C. Reynolds, Marilyn H. Kelly, Panagiota Andreopoulou, Nisan Bhattacharyya, Michael T. Collins, Rachel I Gafni

Publikováno v: Journal of Bone and Mineral Research. 28:1386-1398

Tumor-induced osteomalacia (TIO) is a rare disorder of phosphate wasting due to fibroblast growth factor-23 (FGF23)-secreting tumors that are often difficult to locate. We present a systematic approach to tumor localization and postoperative biochemi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::830cc3954d8dcacaeb6e11e93f4b8fde
https://doi.org/10.1002/jbmr.1881

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Sinonasal Disease in Polyostotic Fibrous Dysplasia and McCune-Albright Syndrome

Autor: Hung Jeffrey Kim, Marilyn H. Kelly, Michael T. Collins, Timothy DeKlotz

Publikováno v: The Laryngoscope. 123:823-828

Objectives/Hypothesis: To characterize the spectrum, symptoms, progression, and effects of endocrine dysfunction on sinonasal disease in polyostotic fibrous dysplasia (PFD) and McCune–Albright Syndrome (MAS). Study Design: Retrospective review. Met

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b41c1531984b816daa582f79cd450ef
https://doi.org/10.1002/lary.23758

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Optic Neuropathy in McCune-Albright Syndrome: Effects of Early Diagnosis and Treatment of Growth Hormone Excess

Autor: H. Jeffrey Kim, John A. Butman, Christopher K. Zalewski, Carolee M. Cutler Peck, McKinley Glover, Edmond J. FitzGibbon, Beth A Brillante, Michael T. Collins, Alison M. Boyce, Carmen C. Brewer, Marilyn H. Kelly

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 98:E126-E134

GH excess is a serious complication of McCune-Albright syndrome (MAS) and has been associated with craniofacial morbidity.The aim of the study was to determine whether early diagnosis and treatment of MAS-associated GH excess prevents optic neuropath

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa1c45d5e9553fcbba6d93607c84ead
https://doi.org/10.1210/jc.2012-2111

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Denosumab treatment for fibrous dysplasia

Autor: William H. Chong, Josephine Z. Kasa-Vubu, Michael T. Collins, Alison M. Boyce, Natasha Cherman, Christine E. Chamberlain, Rachel I Gafni, Michelle Ellsworth, Nisan Bhattacharyya, Carol W. Bassim, Alfredo A. Molinolo, Marilyn H. Kelly, Frances A. Farley, Jack Yao

Publikováno v: Journal of Bone and Mineral Research. 27:1462-1470

Fibrous dysplasia (FD) is a skeletal disease caused by somatic activating mutations of the cyclic adenosine monophosphate (cAMP)-regulating protein, α-subunit of the Gs stimulatory protein (G(s) α). These mutations lead to replacement of normal bon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e1046b19b0f801b2918649a3005f4cb
https://doi.org/10.1002/jbmr.1603

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Selective venous catheterization for the localization of phosphaturic mesenchymal tumors

Autor: Panagiota Andreopoulou, Carolee M. Cutler Peck, Claudia E Dumitrescu, Michael T. Collins, Felasfa M. Wodajo, Richard Chang, Beth A Brillante, Marilyn H. Kelly

Publikováno v: Journal of Bone and Mineral Research

Tumor-induced osteomalacia (TIO) is characterized by renal phosphate wasting, hypophosphatemia, and aberrant vitamin D3 metabolism and is caused by fibroblast growth factor 23 (FGF-23)–producing mesenchymal tumors, which are often difficult to loca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdf26f840fb34a26cc838a661061bfc
https://doi.org/10.1002/jbmr.316

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Cushing Syndrome in the McCune-Albright Syndrome

Autor: Rebecca J. Brown, Marilyn H. Kelly, Michael T. Collins

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 95:1508-1515

Context: Cushing syndrome (CS) is a rare but potentially fatal feature of McCune-Albright syndrome (MAS). Optimal management, prognostic features, and long-term follow-up of this disorder have not been described. Setting: The study was conducted at a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a7c46ae97babb4de7697211581cba3d
https://doi.org/10.1210/jc.2009-2321

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The Role of Type 1 and Type 2 5′-Deiodinase in the Pathophysiology of the 3,5,3′-Triiodothyronine Toxicosis of McCune-Albright Syndrome

Autor: Natasha Cherman, Aaron Chidakel, Beth A Brillante, Francesco S. Celi, Thomas H. Shawker, Giuseppe Coppotelli, Penelope Feuillan, Michael T. Collins, Marilyn H. Kelly

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 93:2383-2389

McCune-Albright syndrome (MAS) is caused by mutations in GNAS (most often R201C or R201H) leading to constitutive cAMP signaling and multiple endocrine dysfunctions, including morphological and functional thyroid involvement.The objective of the stud

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef73a8a196a473375345c5a1dc54a8ea
https://doi.org/10.1210/jc.2007-2237

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Pain in fibrous dysplasia of bone: age-related changes and the anatomical distribution of skeletal lesions

Autor: Michael T. Collins, Beth A Brillante, Marilyn H. Kelly

Publikováno v: Osteoporosis International. 19:57-63

To determine the prevalence, distribution, age-related changes and treatment of pain in fibrous dysplasia, we studied 78 children and adults. Pain was common, more prevalent and intense in adults, sometimes requiring narcotic analgesia. It was often

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e6b0e96eb0fd4d85859209b6d174f55
https://doi.org/10.1007/s00198-007-0425-x

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Onset, Progression, and Plateau of Skeletal Lesions in Fibrous Dysplasia and the Relationship to Functional Outcome

Autor: Marilyn H. Kelly, Beth A Brillante, Clara C. Chen, Arabella I. Leet, Janice S. Lee, Penelope Feuillan, Michael T. Collins, Harvey Kushner, Pamela Gehron Robey, Navid Ziran, Elizabeth S. Hart

Publikováno v: Journal of Bone and Mineral Research. 22:1468-1474

Most lesions in FD and their attendant functional disability occur within the first decade; 90% of lesions are present by 15 years, and the median age when assistive devices are needed is 7 years. These findings have implications for prognosis and de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7f82d84c210af5b6a7b9b5233d9bcb
https://doi.org/10.1359/jbmr.070511

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