Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 77 Records) |
| Query Trace: Disease and PTH[original query] |
|---|
| Serum Parathyroid Hormone, 25-Hydroxyvitamin D, and Risk of Alzheimer's Disease: A Mendelian Randomization Study. Nutrients 2018 Sep 10 (9): . Larsson Susanna C, Traylor Matthew, Markus Hugh S, Michaëlsson Ka |
| Genetic contributors and soluble mediators in prediction of autoimmune comorbidity. Journal of autoimmunity 2019 8 104 102317. Nezos Adrianos, Evangelopoulos Maria-Eleutheria, Mavragani Clio |
| Serum Parathyroid Hormone and Risk of Coronary Artery Disease: Exploring Causality Using Mendelian Randomization. The Journal of clinical endocrinology and metabolism 2019 Jul . Melhus Håkan, Michaëlsson Karl, Larsson Susanna |
| Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
| Pulp chamber features, prevalence of abscesses, disease severity, and PHEX mutation in X-linked hypophosphatemic rickets. Journal of bone and mineral metabolism 2020 8 39 (2): 212-223. Baroncelli Giampiero I, Zampollo Elisa, Manca Mario, Toschi Benedetta, Bertelloni Silvano, Michelucci Angela, Isola Alessandro, Bulleri Alessandra, Peroni Diego, Giuca Maria Ri |
| Vitamin D in Type 2 Diabetes: Genetic Susceptibility and the Response to Supplementation. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2020 Jun . Klahold Edith, Penna-Martinez Marissa, Bruns Franziska, Seidl Christian, Wicker Sabine, Badenhoop Kla |
| CLINICAL AND GENETIC FINDINGS IN A CHINESE COHORT OF PATIENTS WITH DIGEORGE SYNDROME-RELATED HYPOPARATHYROIDISM. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 2 26 (6): 642-650. Wang Yabing, Wang Ou, Nie Min, Li Yuepeng, Jiang Yan, Li Mei, Xia Weibo, Xing Xiaopi |
| Prevalence of Parathyroid Carcinoma and Atypical Parathyroid Neoplasms in 153 Patients With Multiple Endocrine Neoplasia Type 1: Case Series and Literature Review. Frontiers in endocrinology 2020 10 11 557050. Song An, Yang Yi, Liu Shuzhong, Nie Min, Jiang Yan, Li Mei, Xia Weibo, Wang Ou, Xing Xiaopi |
| Study of vitamin D status and vitamin D receptor polymorphisms in a cohort of Italian patients with juvenile idiopathic arthritis. Scientific reports 2020 Oct 10 (1): 17550. Marini Francesca, Falcini Fernanda, Stagi Stefano, Fabbri Sergio, Ciuffi Simone, Rigante Donato, Cerinic Marco Matucci, Brandi Maria Lui |
| Do Patients With Atypical Parathyroid Adenoma Need Close Follow-up? The Journal of clinical endocrinology and metabolism 2021 6 106 (11): e4565-e4579. Saponaro Federica, Pardi Elena, Mazoni Laura, Borsari Simona, Torregrossa Liborio, Apicella Matteo, Frustaci Gianluca, Materazzi Gabriele, Miccoli Paolo, Basolo Fulvio, Marcocci Claudio, Cetani Filome |
| Association of CYP3A5 polymorphisms and parathyroid hormone with blood level of tacrolimus in patients with end-stage renal disease. Clinical and translational science 2021 May . Tanaka Ryota, Suzuki Yosuke, Watanabe Hiroshi, Fujioka Takashi, Hirata Kenshiro, Shin Toshitaka, Ando Tadasuke, Ono Hiroyuki, Tatsuta Ryosuke, Mimata Hiromitsu, Maruyama Toru, Itoh Hiro |
| Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. Journal of nephrology 2021 4 34 (6): 2053-2062. Vall-Palomar Mònica, Burballa Carla, Claverie-Martín Félix, Meseguer Anna, Ariceta Ge |
| Polymorphisms in vitamin D receptor and parathyroid hormone genes in the development and progression of obstructive sleep apnea in Asian Indians. Nutrition (Burbank, Los Angeles County, Calif.) 2021 Mar 89 111237. Bhatt Surya Prakash, Guleria Rande |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Prevalence of hearing loss in pseudohypoparathyroidism. Orphanet journal of rare diseases 2024 9 19 (1): 339. Cassandre Djian, Jugurtha Berkenou, Anya Rothenbuhler, Jérémie Botton, Agnès Linglart, Jérôme Nevo |
| Vitamin D Receptor (VDR) Gene Polymorphisms and High-Turnover Renal Osteodystrophy or Secondary Hyperparathyroidism in End-Stage Renal Disease: A Systematic Review. Cureus 2024 8 16 (7): e64925. Tanya Sinha, Muhammad Muaz Mushtaq, Husnain Ali, Maryyam Liaqat, Maham Mushtaq, Muhammad Ahmad Sarwar, Muhammad Asad Sarwer, Danyal Bakht, Rida Fatima, Syed Faqeer Hussain Bokha |
| Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study. Heliyon 2024 8 10 (14): e34947. Sarra Tombari, Yessine Amri, Yosra Hasni, Sondess Hadj Fredj, Yesmine Salem, Salima Ferchichi, Leila Essaddam, Taieb Messaoud, Rym Dabbou |
| Influence of vitamin D and calcium-sensing receptor gene variants on calcium metabolism in end-stage renal disease: insights from machine learning analysis. European review for medical and pharmacological sciences 2024 12 28 (22): 4634-4643. K Sridharan, A Jassim, A M Qader, M M Qad |
| Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c. Kidney international 2024 10 . Max Brunkhorst, Lena Brunkhorst, Helge Martens, Svetlana Papizh, Martine Besouw, Corinna Grasemann, Serap Turan, Przemyslaw Sikora, Milan Chromek, Elisabeth Cornelissen, Marc Fila, Marc Lilien, Jeremy Allgrove, Thomas J Neuhaus, Mehmet Eltan, Laura Espinosa, Dirk Schnabel, Ibrahim Gokce, Juan David González-Rodríguez, Priyanka Khandelwal, Mandy G Keijzer-Veen, Felix Lechner, Maria Szczepa?ska, Marcin Zaniew, Justine Bacchetta, Francesco Emma, Dieter Haffn |
- Page last reviewed:Feb 1, 2024
- Content source: