Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Osteoporosis and ALPL[original query] |
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[Allele polymorphism of alkaline phosphatase, acid soluble phosphatase, and vitamin D-binding protein genes in postmenopausal osteoporosis]. Terapevticheski? arkhiv 2004 76 (5): 61-5. Krylov M Iu, Korotkova T A, Miakotkin V A, Benevolenskaia L |
Association of ALPL and ENPP1 gene polymorphisms with bone strength related skeletal traits in a Chuvashian population. Bone 2010 May 46 (5): 1244-50. Ermakov Sergey, Toliat Mohammad Reza, Cohen Zvi, Malkin Ida, Altmüller Janine, Livshits Gregory, Nürnberg Pet |
Identification of a p.Arg708Gln variant in COL1A2 in atypical femoral fractures. Joint bone spine 2016 Dec . Funck-Brentano Thomas, Ostertag Agnes, Debiais Francoise, Fardellone Patrice, Collet Corinne, Mornet Etienne, Cohen-Solal Marti |
Loss-of-Function Mutations in the ALPL Gene Presenting with Adult Onset Osteoporosis and Low Serum Concentrations of Total Alkaline Phosphatase. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 Dec . Alonso Nerea, Larraz-Prieto Beatriz, Berg Kathryn, Lambert Zoe, Redmond Paul, Harris Sarah E, Deary Ian J, Pugh Carys, Prendergast James, Ralston Stuart |
Clinical, biochemical and genetic findings in adult patients with chronic hypophosphatasemia. Journal of endocrinological investigation 2021 7 45 (1): 125-137. Guarnieri V, Sileri F, Indirli R, Guabello G, Longhi M, Dito G, Verdelli C, Corbetta |
ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia. The Journal of clinical endocrinology and metabolism 2021 12 107 (5): e2087-e2094. Marini Francesca, Masi Laura, Giusti Francesca, Cianferotti Luisella, Cioppi Federica, Marcucci Gemma, Ciuffi Simone, Biver Emmanuel, Toro Giuseppe, Iolascon Giovanni, Iantomasi Teresa, Brandi Maria Lui |
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis. Bone 2021 11 154 116253. Cohen Adi, Hostyk Joseph, Baugh Evan H, Buchovecky Christie M, Aggarwal Vimla S, Recker Robert R, Lappe Joan M, Dempster David W, Zhou Hua, Kamanda-Kosseh Mafo, Bucovsky Mariana, Stubby Julie, Goldstein David B, Shane Elizabe |
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
Osteoporosis related to WNT1 variants: a not infrequent cause of osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022 11 34 (2): 405-411. Peris Pilar, Monegal Ana, Mäkitie Riikka E, Guañabens Nuria, González-Roca E |
Clinical and Genetic Characteristics of Hypophosphatasia in Chinese Adults. Genes 2023 4 14 (4): . Xiang Li, Na Ren, Ziyuan Wang, Ya Wang, Yunqiu Hu, Weiwei Hu, Jiemei Gu, Wei Hong, Zhenlin Zhang, Chun Wa |
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- Page last updated:Jun 02, 2023
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