Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 370 Records) |
Query Trace: Familial Mediterranean Fever and MEFV[original query] |
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Evaluation of the ischemia modified albumin levels in familial Mediterranean fever patients. Irish journal of medical science 2022 9 . Atabay Yusuf, Alt?n Zeynep, Çolak Ayfer, Akar Har |
The Comparison of Pediatric Patients with Familial Mediterranean Fever Originated from Turkey and Crimea. Turkish archives of pediatrics 2022 9 57 (5): 551-557. Kostik Mikhail, Akca Kaya Ummusen, Zhogova Olga V, Sag Erdal, Suspitsin Evgeny N, Nizhnik Viktoriya I, Tumakova Anastasiya V, Ivanovskiy Sergey V, Lagunova Natalia V, Bilginer Yelda, Ozen Se |
Can RDW be used as a screening test for subclinical inflammation in children with FMF? Is RDW related to MEFV gene mutations? Clinical rheumatology 2022 9 42 (1): 197-202. Parmaks?z Gönül, Noyan Z Ayt |
Early Predictors of Colchicine Resistance in Familial Mediterranean Fever. Modern rheumatology 2022 7 . Mosad Mosa Doaa, Shokry Doaa, Ahmed Dina B, Sobh A |
R202Q prevalence in clinically diagnosed Familial Mediterranean Fever patients: 9 years of data analysis from 1570 patients living Central Black Sea region, Turkey. Irish journal of medical science 2022 11 . Çapraz Mustafa, Düz Muhammed Em |
Occurrence of familial Mediterranean fever in haemophilia patients. Haemophilia : the official journal of the World Federation of Hemophilia 2022 11 29 (1): 165-171. Kirkiz Serap, Kaya Zühre, Gönen Sevim, Ya?c? Münci, Koçak Ülk |
Does having MEFV gene sequence variants affect the clinical course and colchicine response in children with PFAPA syndrome? European journal of pediatrics 2022 11 182 (1): 411-417. Otar Yener Gülçin, Akta? ?lke, Alt?nta? Me?e Ceren, Çakan Musta |
Recurrent Fever with Oral Lesions in Egyptian Children: A Familial Mediterranean Fever Diagnosis Not to Be Missed. Children (Basel, Switzerland) 2022 11 9 (11): . Omran Ahmed, Abdelrahman Ahmed, Mohamed Yasmine Gabr, Abdalla Mohamed Osama, Abdel-Hamid Eman R, Elfiky Sam |
Role of non-invasive methods in detecting liver impairment in familial Mediterranean fever adult patients with persistent hepatic cytolysis. Scientific reports 2022 10 12 (1): 16644. Deshayes Samuel, Fraisse Thibault, Fellahi Soraya, Steichen Olivier, Savey Léa, Turlin Bruno, Munteanu Mona, Aouba Achille, Bourguiba Rim, Hentgen Véronique, Faintuch Jean-Manuel, Giurgea Irina, Grateau Gilles, Bastard Jean-Philippe, Georgin-Lavialle Soph |
The effect of a 18?bp deletion/insertion variant of VEGF gene on the FMF development. Nucleosides, nucleotides & nucleic acids 2022 10 1-12. Sezer Ozlem, Nursal Ayse Feyda, Kuruca Nilufer, Yigit Serbule |
Utility of a targeted next-generation sequencing-based genetic screening panel in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome. Archives of rheumatology 2023 9 38 (2): 299-306. Rabia Miray K??la Ekinci, Özlem Anla?, Özge Öza |
Hyperinflammatory Immune Response in COVID-19: Host Genetic Factors in Pyrin Inflammasome and Immunity to Virus in a Spanish Population from Majorca Island. Biomedicines 2023 9 11 (9): . Natalia Martínez-Pomar, Vanesa Cunill, Marina Segura-Guerrero, Elisabet Pol-Pol, Danilo Escobar Oblitas, Jaime Pons, Ignacio Ayestarán, Patricia C Pruneda, Inés Losada, Nuria Toledo-Pons, Mercedes García Gasalla, Joana Maria Ferrer Balagu |
Clinical presentation and genetic variants in patients with autoinflammatory diseases: results from the German GARROD registry. Rheumatology international 2023 9 . Norbert Blank, Ina Kötter, Marc Schmalzing, Jürgen Rech, Karoline Krause, Birgit Köhler, Dorothee Kaudewitz, Martin Nitschke, Christian S Haas, Hanns-Martin Lorenz, Martin Krusc |
Characteristics and course of patients with AA Amyloidosis: single center experience with 174 patients from Turkey. Rheumatology (Oxford, England) 2023 9 . Murat Bektas, Nevzat Koca, Emin Oguz, Selma Sari, Gizem Dagci, Burak Ince, Pelin Karaca Ozer, Besim Fazil Agargun, Yasemin Yalcinkaya, Bahar Artim-Esen, Lale Ocal, Murat Inanc, Ahmet G |
Clinical features, functional status, and quality of life in patients with late-onset familial Mediterranean fever. Northern clinics of Istanbul 2023 9 10 (4): 451-457. Didem Erdem Gursoy, Halise Hande Gezer, Nuran Oz, Aygun Ozer, Sevtap Acer Kasman, Mehmet Tuncay Duru |
Gut microbiota alterations are associated with phenotype and genotype in familial Mediterranean fever. Rheumatology (Oxford, England) 2023 7 . Marion Delplanque, Nicolas Benech, Nathalie Rolhion, Cyriane Oeuvray, Marjolène Straube, Chloé Galbert, Loic Brot, Thomas Henry, Yvan Jamilloux, Léa Savey, Gilles Grateau, Harry Sokol, Sophie Georgin-Lavial |
Investigation of different genomic variants in familial Mediterranean fever cases with monoallelic MEFV mutation. Clinical and experimental rheumatology 2023 5 . Mehmet Kocabey, Tufan Cankaya, Meral Torum Bayram, Ayfer Ulgenalp, Ahmet Okay Caglayan, Ozlem Giray Bozka |
Genetic and clinical features of familial mediterranean fever (FMF) in a homogeneous cohort of patients from South-Eastern Italy. European journal of internal medicine 2023 5 . Agostino Di Ciaula, Matteo Iacoviello, Leonilde Bonfrate, Mohamad Khalil, Harshitha Shanmugam, Giuseppe Lopalco, Rosanna Bagnulo, Antonella Garganese, Florenzo Iannone, Nicoletta Resta, Piero Portincasa, Alessandro Stel |
Genotype-Phenotype Associations of Children With Familial Mediterranean Fever in a Cohort Consisted of M694V and Implications for Colchicine-Resistant Disease. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases 2023 3 . Kisaoglu Hakan, Baba Ozge, Kalyoncu Mukadd |
IgA Vasculitis in Japanese Patients Harboring MEFV Mutations: A Case Report and Review of the Literature. Cureus 2023 3 15 (2): e34876. Yokoyama Tadafumi, Sakumura Naoto, Inoue Natsumi, Matsuda Yusuke, Wada Tai |
Genotype Mutations in Palestinian Children with Familial Mediterranean Fever: Clinical Profile, and Response to Colchicine Treatment: A Retrospective Cohort Study. Mediterranean journal of rheumatology 2023 11 34 (3): 332-341. Oadi N Shrateh, Mariam Thalji, Afnan W M Jobran, Aml M Brakat, Abdelrahman M Attia, Fawzy M Abunej |
Colitis in a patient with familial Mediterranean fever: Is it Crohn's disease or ulcerative colitis? DEN open 2024 9 5 (1): e70013. Ayano Hoshi, Yuichi Shimodate, Tatsuhiro Gotoda, Rio Takezawa, Naoyuki Nishimura, Hirokazu Mouri, Kazuhiro Matsueda, Motowo Mizuno, Takayuki Matsumo |
The Impact of Different MEFV Genotypes on Clinical Phenotype of Patients with Familial Mediterranean Fever: Special Emphasis on Joint Involvement. European journal of pediatrics 2024 8 . Esma Aslan, Nergis Akay, Umit Gul, Elif Kilic Konte, Aybuke Gunalp, Fatih Haslak, Amra Adrovic, Kenan Barut, Mehmet Yildiz, Sezgin Sahin, Ozgur Kasapcop |
The increased chromosomal DNA damage in patients with Familial Mediterranean Fever. Biotechnic & histochemistry : official publication of the Biological Stain Commission 2024 8 1-8. Aslihan Kiraz, Hamiyet Eciroglu, P?nar Altin-Celik, Hamiyet Donmez-Altunt |
E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant? European journal of pediatrics 2024 8 . Elham Orouk Awaad, Lana Khoury, Joeri W van Straalen, Adi Miller-Barmak, Tal Gazitt, Jumana Haddad-Haloun, Riva Brik, Mohamad Hamad Sai |
Plasminogen activator inhibitor-1 genotype 4G/5G associates with skin involvement in Armenian familial Mediterranean fever patients. Rheumatology international 2024 7 . Gernot Kriegshäuser, Hasmik Hayrapetyan, Christian Oberkanins, Tamara Sarkisi |
Molecular analyses of MEFV gene mutation variants in Turkish population. Molecular biology reports 2024 7 51 (1): 844. Rahime Aksoy, Ebru Us, Darya Farhoomand Aksoy, Ebru Dumlup?nar, Tahsin Murat Turg |
The significance of carrying MEFV variants in symptomatic and asymptomatic individuals. Clinical genetics 2024 5 . Eldad Ben-Chetrit, Isabelle Touit |
High frequency of MEFV disease-causing variants in children with very-early-onset inflammatory bowel disease. Pediatric research 2024 5 . Aasem Abu Shtaya, Naama Orenstein, Lily Bazak, Gabriel Lidzbarsky, Marina Lifshitc Kalis, Gil Amarilyo, Efrat Sofrin-Drucker, Ranit Jaron, Noa Ruhrman Shahar, Nesia Kropach Gilad, Lina Basel-Salm |
Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children. Heliyon 2024 4 10 (8): e29469. Yang Ruan, Longlong X |
- Page last reviewed:Feb 1, 2024
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