Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 41 Records) |
| Query Trace: Disease and AIP[original query] |
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| Association of the ZFPM2 gene with antipsychotic-induced parkinsonism in schizophrenia patients. Psychopharmacology 2012 Apr 220 (3): 519-28. Greenbaum Lior, Smith Robert C, Lorberboym Mordechai, Alkelai Anna, Zozulinsky Polina, Lifschytz Tzuri, Lifshytz Tzuri, Kohn Yoav, Djaldetti Ruth, Lerer Berna |
| AHR over-expression in papillary thyroid carcinoma: clinical and molecular assessments in a series of Italian acromegalic patients with a long-term follow-up. PloS one 2014 9 (7): e101560. Mian Caterina, Ceccato Filippo, Barollo Susi, Watutantrige-Fernando Sara, Albiger Nora, Regazzo Daniela, de Lazzari Paola, Pennelli Gianmaria, Rotondi Sandra, Nacamulli Davide, Pelizzo Maria Rosa, Jaffrain-Rea Marie-Lise, Grimaldi Franco, Occhi Gianluca, Scaroni Car |
| Human cationic trypsinogen but not serine peptidase inhibitor, Kazal type 1 variants increase the risk of type 1 autoimmune pancreatitis. Journal of gastroenterology and hepatology 2014 Dec 29 (12): 2038-42. Chang Ming-Chu, Jan I-Shiow, Liang Po-Chin, Jeng Yung-Ming, Yang Ching-Yao, Tien Yu-Wen, Wong Jau-Min, Chang Yu-Ti |
| Mutation analysis of inhibitory guanine nucleotide binding protein alpha (GNAI) loci in young and familial pituitary adenomas. PloS one 2014 9 (10): e109897. Demir Hande, Donner Iikki, Kivipelto Leena, Kuismin Outi, Schalin-Jäntti Camilla, De Menis Ernesto, Karhu Au |
Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis.
PloS one 2015 10 (5): e0127078. Oguchi Takaya, Ota Masao, Ito Tetsuya, Hamano Hideaki, Arakura Norikazu, Katsuyama Yoshihiko, Meguro Akira, Kawa Shigeyu |
| AIP mutations in young patients with acromegaly and the Tampico Giant: the Mexican experience. Endocrine 2016 Mar . Ramírez-Rentería Claudia, Hernández-Ramírez Laura C, Portocarrero-Ortiz Lesly, Vargas Guadalupe, Melgar Virgilio, Espinosa Etual, Espinosa-de-Los-Monteros Ana Laura, Sosa Ernesto, González Baldomero, Zúñiga Sergio, Unterländer Martina, Burger Joachim, Stals Karen, Bussell Anne-Marie, Ellard Sian, Dang Mary, Iacovazzo Donato, Kapur Sonal, Gabrovska Plamena, Radian Serban, Roncaroli Federico, Korbonits Márta, Mercado Mois |
| A Variant of Peptide Transporter 2 Predicts the Severity of Porphyria-Associated Kidney Disease. Journal of the American Society of Nephrology : JASN 2016 Dec . Tchernitchko Dimitri, Tavernier Quentin, Lamoril Jérôme, Schmitt Caroline, Talbi Neila, Lyoumi Said, Robreau Anne-Marie, Karim Zoubida, Gouya Laurent, Thervet Eric, Karras Alexandre, Puy Hervé, Pallet Nicol |
| Paraoxonase 1 (PON1) Q192R genotypes and their interaction with smoking strongly increase atherogenicity and the Framingham risk score. Archives of endocrinology and metabolism 2016 Oct 60 (5): 426-435. Souza-Nogueira Andre de, Camargo Alissana Ester, Remondi Felipe Assan, Paoliello Monica Maria Bastos, Richter Rebecca J, Furlong Clement E, Barbosa Decio Sabbatini, Maes Michael, Moreira Estefania Gastaldel |
| Association of the Apolipoprotein A-I Gene Polymorphisms with Cardiovascular Disease Risk Factors and Atherogenic Indices in Patients from Assam, Northeast India. Balkan journal of medical genetics : BJMG 2017 Jun 20 (1): 59-70. Bora K, Pathak M S, Borah P, Hussain Md I, Das |
| Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. PloS one 2017 10 12 (10): e0186485. Pardi Elena, Borsari Simona, Saponaro Federica, Bogazzi Fausto, Urbani Claudio, Mariotti Stefano, Pigliaru Francesca, Satta Chiara, Pani Fabiana, Materazzi Gabriele, Miccoli Paolo, Grantaliano Lorena, Marcocci Claudio, Cetani Filome |
| Serum PCSK9 levels, but not PCSK9 polymorphisms, are associated with CAD risk and lipid profiles in southern Chinese Han population. Lipids in health and disease 2018 Sep 17 (1): 213. Cai Gaojun, Yu Lei, Huang Zhiying, Li Li, Fu Xing |
| Co-occurrence of MEN1 p.Gly111fs and AIP p.Arg16His Variants in Familial MEN1 Phenotype. Anticancer research 2018 Jun 38 (6): 3683-3687. DE Melo Flavia Marques, Bastos-Rodrigues Luciana, Sarquis Maria Marta, Friedman Eitan, DE Marco Lu |
| In vivo bioassay to test the pathogenicity of missense human AIP variants. Journal of medical genetics 2018 4 55 (8): 522-529. Aflorei Elena Daniela, Klapholz Benjamin, Chen Chenghao, Radian Serban, Dragu Anca Neluta, Moderau Nina, Prodromou Chrisostomos, Ribeiro Paulo S, Stanewsky Ralf, Korbonits Már |
| Gender specific effect of CETP rs708272 polymorphism on lipid and atherogenic index of plasma levels but not on the risk of coronary artery disease: A case-control study. Medicine 2018 Dec 97 (49): e13514. Cai Gaojun, Shi Ganwei, Huang Zhiyi |
| Genotype and phenotype of salt-stimulated paraoxonase 1 (PON1) is associated with atherogenic indices in type 2 diabetes. Journal of diabetes and metabolic disorders 2018 10 17 (1): 1-10. Qujeq Durdi, Mahrooz Abdolkarim, Alizadeh Ahad, Masoumi Parisa, Annemohammadzadeh Saleh, Boorank Ruzb |
| Atherogenic index of plasma as a cardiovascular risk marker in manic, depressive, and euthymic stages of bipolar disorder. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2018 1 46 (1): 32-38. Kalelio?lu Tevfik, Ünalan Pelin, Kök Burcu, Sözen ?ule, Yüksel Özge, Akku? Mustafa, Cihnio?lu Refik, Karamustafal?o?lu Nesr |
| High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor. Orphanet journal of rare diseases 2019 2 14 (1): 59. Barreda-Sánchez María, Buendía-Martínez Juan, Glover-López Guillermo, Carazo-Díaz Carmen, Ballesta-Martínez María Juliana, López-González Vanesa, Sánchez-Soler María José, Rodriguez-Peña Lidya, Serrano-Antón Ana Teresa, Gil-Ferrer Remedios, Martínez-Romero Maria Del Carmen, Carbonell-Meseguer Pablo, Guillén-Navarro Encar |
| Systematically Analyzing the Pathogenic Variations for Acute Intermittent Porphyria. Frontiers in pharmacology 2019 10 10 1018. Fu Yibao, Jia Jinmeng, Yue Lishu, Yang Ruiying, Guo Yongli, Ni Xin, Shi Tiel |
| Three Novel MEN1 Variants in AIP-Negative Familial Isolated Pituitary Adenoma Patients. Pathobiology : journal of immunopathology, molecular and cellular biology 2019 Jan 1-7. Yarman Sema, Tuncer Feyza Nur, Serbest Es |
| SNPs of miR-23b, miR-107 and HMGA2 and their Relations with the Response to Medical Treatment in Acromegaly Patients. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2020 Aug . Armagan Derya Metin, Akdemir Ayse Seda, Ozkaya Hande Mefkure, Korkmaz Ozge Polat, Gazioglu Nurperi, Kadioglu Pinar, Tanriover Necmettin, Dagistanli Kaya-Fatma, Dirican Ahmet, Ozturk Mel |
| Phenotypic and genotypic features of a large kindred with a germline AIP variant. Clinical endocrinology 2020 4 93 (2): 146-153. Dal Jakob, Nielsen Eigil H, Klose Marianne, Feldt-Rasmussen Ulla, Andersen Marianne, Vang Søren, Korbonits Márta, Jørgensen Jens Otto |
| Interaction between dietary total antioxidant capacity and BDNF Val66Met polymorphism on lipid profiles and atherogenic indices among diabetic patients. Scientific reports 2021 Sep 11 (1): 19108. Abaj Faezeh, Rafiee Masoumeh, Koohdani Fari |
| Clinical and genetic characteristics in patients under 30 years with sporadic pituitary adenomas. European journal of endocrinology 2021 7 185 (4): 485-496. Martínez de LaPiscina Idoia, Portillo Najera Nancy, Rica Itxaso, Gaztambide Sonia, Webb Susan M, Santos Alicia, Moure Maria Dolores, Paja Fano Miguel, Hernandez Maria Isabel, Chueca-Guindelain Maria Jesús, Hernández-Ramírez Laura Cristina, Soto Alfonso, Valdés Nuria, Castaño Lu |
| Dysregulation of homocysteine homeostasis in acute intermittent porphyria patients receiving heme arginate or givosiran. Journal of inherited metabolic disease 2021 4 44 (4): 961-971. To-Figueras Jordi, Wijngaard Robin, García-Villoria Judit, Aarsand Aasne K, Aguilera Paula, Deulofeu Ramon, Brunet Mercè, Gómez-Gómez Àlex, Pozo Oscar J, Sandberg Sver |
| HLA-DRB1?16 and -DQB1?05 alleles are strongly associated with autoimmune pancreatitis in a cohort of hundred patients. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2022 4 22 (4): 466-471. Goni Elisabetta, Regel Ivonne, Mahajan Ujjwal Mukund, Amodio Antonio, De Marchi Giulia, Beyer Georg, Zuppardo Raffaella Alessia, Di Leo Milena, Lanzillotta Marco, Bonatti Francesco, Kauke Teresa, Dick Andrea, Weiss Frank Ulrich, Schönermarck Ulf, Lerch Markus M, Frulloni Luca, Cavestro Giulia Martina, Mayerle Jul |
| Heterogeneous molecular behavior in liver tumors (HCC and CCA) of two patients with acute intermittent porphyria. Journal of cancer research and clinical oncology 2022 10 . Haverkamp Thomas, Bronisch Olivia, Knösel Thomas, Mogler Carolin, Weichert Wilko, Stauch Thomas, Schmid Claudia, Rummeny Claudia, Beykirch Maria K, Petrides Petro |
| Genomic profiling of primary diffuse large B-cell lymphoma of the central nervous system suggests novel potential therapeutic targets. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 9 100323. Claudio Agostinelli, Luca Morandi, Simona Righi, Luigi Cirillo, Marica Iommi, Caterina Tonon, Diego Mazzatenta, Matteo Zoli, Maura Rossi, Gianmarco Bagnato, Alessandro Broccoli, Raffaele Lodi, Pier Luigi Zinzani, Elena Sabattini, Caterina Giannini, Sofia Asio |
| Genetic Determinants of Atherogenic Indexes. Genes 2023 6 14 (6): . Tomas Texis, Susana Rivera-Mancía, Eloisa Colín-Ramírez, Raul Cartas-Rosado, David Koepsell, Kenneth Rubio-Carrasco, Mauricio Rodríguez-Dorantes, Vanessa Gonzalez-Covarrubi |
| 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 |
| Polymorphisms rs562556 and rs2479409 of the PCSK9 gene associated with obesity and cardiovascular disease. Central European journal of public health 2024 1 31 (Suppl 1): S82-S88. Hedviga Vašková, Janka Porá?ová, Miriama Šlebodová, So?a Kalafutová, Mária Kone?ná, Vincent Sedlák, Tatiana Kimáková, Marta Mydlárová Blaš?áko |
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