Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 234 Records) |
Query Trace: PTH[original query] |
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The impact of CASR A990G polymorphism in response to cinacalcet treatment in hemodialysis patients with secondary hyperparathyroidism. Scientific reports 2021 Sep 11 (1): 18006. Ngamkam Jaruwan, Vadcharavivad Somratai, Areepium Nutthada, Auamnoy Titinun, Takkavatakarn Kullaya, Katavetin Pisut, Tiranathanagul Khajohn, Praditpornsilpa Kearkiat, Eiam-Ong Somchai, Susantitaphong Pawee |
The Effect of the Severity of Obstructive Sleep Apnea on Leukocyte Telomere Length, 25 Hydroxy Vitamin D, and Parathyroid Hormonal Concentrations in Asian Indians. Frontiers in neurology 2021 11 12 682739. Bhatt Surya Prakash, Guleria Randeep, Vikram Naval |
Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in endocrinology 2021 11 12 736240. Molin Arnaud, Lemoine Sandrine, Kaufmann Martin, Breton Pierre, Nowoczyn Marie, Ballandonne Céline, Coudray Nadia, Mittre Hervé, Richard Nicolas, Ryckwaert Amélie, Lavillaureix Alinoe, Jones Glenville, Bacchetta Justine, Kottler Marie-Lau |
The impact of serum 25-hydroxyvitamin D, calcium, and parathyroid hormone levels on the risk of coronary artery disease in patients with diabetes: a Mendelian randomization study. Nutrition journal 2021 10 20 (1): 82. Chen Songzan, Yang Fangkun, Xu Tian, Wang Yao, Zhang Kaijie, Fu Guosheng, Zhang Wenb |
Calcium, Its Regulatory Hormones, and Their Causal Role on Blood Pressure: A Two-Sample Mendelian Randomization Study. The Journal of clinical endocrinology and metabolism 2022 9 107 (11): 3080-3085. Giontella Alice, Lotta Luca A, Baras Aris, Minuz Pietro, Gill Dipender, Melander Olle, Fava Cristia |
Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia. Pediatric nephrology (Berlin, Germany) 2022 9 38 (4): 1067-1073. Gurevich Evgenia, Borovitz Yael, Levi Shelli, Perlman Sharon, Landau Dani |
Observations from a prospective small cohort study suggest that CGRP genes contribute to acute posttraumatic headache burden after concussion. Frontiers in neurology 2022 13 947524. La Fountaine Michael F, Hohn Asante N, Leahy Caroline L, Weir Joseph P, Testa Anthony |
Galectin 3 (LGALS3) Gene Polymorphisms Are Associated with Biochemical Parameters and Primary Disease in Patients with End-Stage Renal Disease in Serbian Population. Journal of clinical medicine 2022 Jul 11 (13): . Kovacevic Zoran, Lazarevic Tatjana, Maksimovic Nela, Grk Milka, Volarevic Vladislav, Gazdic Jankovic Marina, Djukic Svetlana, Janicijevic Katarina, Miletic Kovacevic Marina, Ljujic Bilja |
A Molecular Insight of the Role of PIN-1 Promoter Polymorphism (- 667C?>?T; rs2233679) in Chronic Kidney Disease Patients with Secondary Hyperparathyroidism. Indian journal of clinical biochemistry : IJCB 2022 Jul 37 (3): 319-327. Patel Digishaben D, Parchwani Deepak, Vachhani Uday, Parchwani Tanishk, Raghavani Pratik, Rajput Ajay, Dholariya Sagar, Singh Ragi |
Association of Serum 25(OH)D with Metabolic Syndrome in Chinese Women of Childbearing Age. Nutrients 2022 May 14 (11): . Shan Xiaoyun, Zhao Xiayu, Li Siran, Song Pengkun, Man Qingqing, Liu Zhen, Hu Yichun, Yang Lich |
An association of VDR gene polymorphism in hypovitaminosis D mediated secondary hyperparathyroidism in adolescent girls; a tertiary hospital study in central India. Steroids 2022 6 185 109054. Chowdhary R, Khan R B, Masarkar N, Malik R, Goel S |
Genetic Variants Associated With Mineral Metabolism Traits in Chronic Kidney Disease. The Journal of clinical endocrinology and metabolism 2022 May . Laster Marciana L, Rowan Bryce, Chen Hua-Chang, Schwantes-An Tae-Hwi, Sheng Xin, Friedman Peter A, Ikizler T Alp, Sinshiemer Janet S, Ix Joachim H, Susztak Katalin, de Boer Ian H, Kestenbaum Bryan, Hung Adriana, Moe Sharon M, Perwad Farzana, Robinson-Cohen Cassian |
Novel mutations of the calcium-sensing receptor impede differential diagnosis of primary hyperparathyroidism and familial hypocalciuric hypercalcemia. Gland surgery 2022 3 11 (1): 12-22. Bhangu Jagdeep Singh, Baumgartner-Parzer Sabina, Hargitai Lindsay, Mazal Peter, Scheuba Christian, Riss Phili |
Osteoporosis and its Association with Vitamin D Receptor, Oestrogen ? Receptor, Parathyroid Receptor and Collagen Type I alpha Receptor Gene Polymorphisms with Bone Mineral Density: A Pilot Study from South Indian Postmenopausal Women of Tamil Nadu. Biochemical genetics 2022 Feb . Fernandez Chrisanne, Tennyson Jebasingh, Priscilla A |
The association of thrombophilia in women with severe obstetric complications. Journal of medicine and life 2022 11 15 (10): 1299-1304. Alzahrani Faisal Mousa, Al-Mulhim Abdulaziz, Shaikh Saeed Sattar, Aldossary Maryam Ahmed, Aldarmahi Ahmed, Alnaam Yaser, Al-Jamea Lamiaa Hammad, Al-Maqati Thekra, Elnagi Elmoeiz, Hassan Fathelrahman Mahdi, Muzahee |
Lack of secondary hyperparathyroidism in sub-group of vitamin D deficient postmenopausal women: Is VDR gene polymorphism behind this mystery? Diabetes & metabolic syndrome 2022 1 16 (1): 102381. Dixit Vivek, Tripathi R L, Dhanwal Dinesh Kum |
PTHR1 Genetic Polymorphisms Are Associated with Osteoporosis among Postmenopausal Arab Women. BioMed research international 2022 1 2021 2993761. Abdi Saba, Almiman Abeer Abdulaziz, Ansari Mohammed Ghouse Ahmed, Alnaami Abdullah M, Mohammed Abdul Khader, Aljohani Naji J, Alenad Amal, Alghamdi Amani, Alokail Majed S, Al-Daghri Nasser |
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders. European journal of endocrinology 2022 1 186 (3): 351-366. Canaff Lucie, Guarnieri Vito, Kim Yoojung, Wong Betty Y L, Nolin-Lapalme Alexis, Cole David E C, Minisola Salvatore, Eller-Vainicher Cristina, Cetani Filomena, Repaci Andrea, Turchetti Daniela, Corbetta Sabrina, Scillitani Alfredo, Goltzman Dav |
Vitamin D receptor gene polymorphisms in chronic kidney disease Egyptian children: effect on biochemical markers of bone mineral disorders. Pediatric endocrinology, diabetes, and metabolism 2022 28 (3): 188-196. F Elshamaa Manal, Eryan Eman, Hamed Hanan, Khalifa Iman, Kamel Solaf, Ibrahim Mona H, Kandil Dina, Farouk Hebatallah, Raafat Mona, Abd-El Haleem Dalia A, Mahmoud Eman, El-Saeed Gamila, Abo Hashish Maha, Abd Elhamid Enas, Sayed Shaim |
Evaluation of effects of indoxyl sulfate and parathyroid hormone on CYP3A activity considering the influence of CYP3A5 gene polymorphisms. British journal of clinical pharmacology 2023 7 . Ayako Oda, Yosuke Suzuki, Chisato Yoshijima, Haruki Sato, Ryota Tanaka, Hiroyuki Ono, Ryosuke Tatsuta, Tadasuke Ando, Toshitaka Shin, Hiroki Itoh, Keiko Oh |
A Pilot Study of the Association VDR Polymorphisms With Primary Hyperparathyroidism. In vivo (Athens, Greece) 2023 4 37 (3): 1111-1116. Angeliki Chorti, Charoula Achilla, Despoina Tsalkatidou, Moysis Moysidis, Angeliki Cheva, Anthoula Chatzikyriakidou, Theodosios Papavramid |
Polymorphisms in hormonal-related genes might be associated with variations in permanent tooth crown size. Orthodontics & craniofacial research 2023 2 . Gerber Jennifer Tsi, Weiss Suyany Gabriely, Mijolaro Laura Vidal, Silva Carolina Siqueira, Petinati Maria Fernanda Pivetta, Meger Michelle Nascimento, Honório Heitor Marques, Rebellato Nelson Luis Barbosa, Sebastiani Aline Monise, Küchler Erika Calvano, Scariot Rafae |
Vitamin D and Bone Metabolism in Adult Patients with Neurofibromatosis Type 1. Metabolites 2023 2 13 (2): . Modica Roberta, Altieri Barbara, D'Aniello Francesco, Benevento Elio, Cannavale Giuseppe, Minotta Roberto, Liccardi Alessia, Colao Annamaria, Faggiano Antongiul |
Familial parathyroid tumours-comparison of clinical profiles between syndromes. Journal of endocrinological investigation 2023 2 . Figueiredo A A, Saramago A, Cavaco B M, Simões-Pereira J, Leite |
Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort. Frontiers in endocrinology 2023 2 14 1027598. Chen Yingyu, Song An, Nie Min, Jiang Yan, Li Mei, Xia Weibo, Wang Ou, Xing Xiaopi |
Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. Frontiers in endocrinology 2023 10 14 1244361. Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rig |
A genetic study of a Brazilian cohort of patients with X-linked hypophosphatemia reveals no correlation between genotype and phenotype. Frontiers in pediatrics 2023 10 11 1215952. Mauro Borghi, Leopoldo Muniz da Silva, Luciana Bispo, Carlos A Long |
Biochemical markers and FokI and TaqI vitamin D receptor genes polymorphism in rheumatoid arthritis. BMC medical genomics 2023 10 16 (1): 252. Hosam M Ahmad, Zaki M Zaki, Asmaa S Mohamed, Amr E Ahm |
Some genetic differences in patients with rheumatoid arthritis. BMC research notes 2023 10 16 (1): 274. Hosam M Ahmad, Zaki M Zaki, Asmaa S Mohamed, Amr E Ahm |
Phosphoproteomics implicates glutamatergic and dopaminergic signalling in the antidepressant-like properties of the iron chelator deferiprone. Neuropharmacology 2024 1 109837. Volkan Uzungil, Sandra Luza, Carlos M Opazo, Isaline Mees, Shanshan Li, Ching-Seng Ang, Nicholas A Williamson, Ashley I Bush, Anthony J Hannan, Thibault Reno |
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- Page last updated:Apr 22, 2024
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