Michael T Collins
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Explore the profile of Michael T Collins including associated specialties, affiliations and a list of published articles.
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253
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5838
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Recent Articles
1.
Jimenez M, Sheppard A, Jaimovich R, Covarrubias N, Jordan D, Quintana J, et al.
Calcif Tissue Int
. 2025 Jan;
116(1):34.
PMID: 39864041
X-linked hypophosphatemia (XLH) is a rare metabolic disorder characterized by elevated FGF23 and chronic hypophosphatemia, leading to impaired skeletal mineralization and enthesopathies that are associated with pain, stiffness, and diminished...
2.
Obiezu F, Almpani K, Kim H, Zalewski C, Chu E, Jahanmir G, et al.
JBMR Plus
. 2025 Jan;
9(2):ziae156.
PMID: 39830149
Jansen metaphyseal chondrodysplasia (JMC) is an ultra-rare disorder caused by constitutive activation of parathyroid hormone type 1 receptor (PTH1R). We sought to characterize the craniofacial phenotype of patients with the...
3.
Lewiecki E, Bilezikian J, Clark A, Collins M, Kado D, Lane J, et al.
J Clin Densitom
. 2025 Jan;
28(1):101559.
PMID: 39826229
The 24 Annual Santa Fe Bone Symposium (SFBS) was held in Santa Fe, New Mexico, USA, on August 2-3, 2024. This was a "hybrid" meeting, with in-person and real-time remote...
4.
Patil M, Wangsiricharoen S, Lazar A, Moon B, Madewell J, Collins M, et al.
JBMR Plus
. 2024 Dec;
9(1):ziae145.
PMID: 39664934
Dysregulated FGF23 production is a demonstrated cause of hypophosphatemia and osteomalacia. Diseases associated with these conditions include phosphaturic mesenchymal tumor (PMT) causing tumor induced osteomalacia, various forms of rickets, and...
5.
Raborn L, Michel Z, Collins M, Boyce A, de Castro L
Cells
. 2024 Sep;
13(17.
PMID: 39273006
Fibrous dysplasia (FD) is a mosaic skeletal disorder involving the development of benign, expansile fibro-osseous lesions during childhood that cause deformity, fractures, pain, and disability. There are no well-established treatments...
6.
Obiezu F, Magone De Quadros Costa M, Huryn L, Pan K, Almpani K, Ninan A, et al.
JBMR Plus
. 2024 Aug;
8(9):ziae089.
PMID: 39108358
Jansen metaphyseal chondrodysplasia (JMC) is an ultra-rare disorder caused by germline heterozygous variants resulting in constitutive activation of parathyroid hormone type 1 receptor. A description of ocular manifestations of the...
7.
Kravitz A, Liao M, Morota G, Tyler R, Cockrum R, Manohar B, et al.
Int J Mol Sci
. 2024 Jul;
25(14).
PMID: 39062990
Johne's disease (JD), also known as paratuberculosis, is a chronic, untreatable gastroenteritis of ruminants caused by subsp. (MAP) infection. Evidence for host genetic resistance to disease progression exists, although it...
8.
Sheppard A, Paravastu S, Farhadi F, Donnelly E, Hartley I, Gafni R, et al.
J Bone Miner Res
. 2024 Jul;
39(9):1327-1339.
PMID: 39046425
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare disorder caused by deficient FGF23 signaling and resultant ectopic calcification. Here, we systematically characterized and quantified macro- and micro-calcification in a HFTC...
9.
Michel Z, Raborn L, Spencer T, Pan K, Martin D, Roszko K, et al.
Cells
. 2024 May;
13(9.
PMID: 38727310
Fibrous dysplasia (FD) is a mosaic skeletal disorder caused by somatic activating variants of encoding for Gα and leading to excessive cyclic adenosine monophosphate signaling in bone-marrow stromal cells (BMSCs)....
10.
Sheppard A, Theng E, Paravastu S, Wojnowski N, Farhadi F, Morris M, et al.
Arterioscler Thromb Vasc Biol
. 2024 Apr;
44(6):1432-1446.
PMID: 38660800
Background: Vascular calcification causes significant morbidity and occurs frequently in diseases of calcium/phosphate imbalance. Radiolabeled sodium fluoride positron emission tomography/computed tomography has emerged as a sensitive and specific method for...