Zobrazeno 1 - 10
of 1 072
pro vyhledávání: '"FOP"'
Autor:
Yodit Abraham Yaynishet, Fathia Omer Salah, Bemnet Taye Gebregiorgis, Abdulmejid Suleyman Mume, Henok Dessalegn Damtew, Tinsae Zelalem Amare, Tilahun Mengistu Manaleh
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 2973-2977 (2024)
Fibrodysplasia ossificans progressiva (FOP) is a rare and progressively debilitating disorder affecting 1 in 2 million individuals. It is characterized by the progressive ossification of soft tissues into ectopic bone and congenital malformations of
Externí odkaz:
https://doaj.org/article/47c367b6d397431bbe33697754f08253
Autor:
Roberta Zupo, Fabio Castellana, Prisco Piscitelli, Pasquale Crupi, Addolorata Desantis, Enrico Greco, Franca Paola Severino, Manuela Pulimeno, Andrea Guazzini, Tassos C. Kyriakides, Vasilis Vasiliou, Antonia Trichopoulou, Laura Soldati, Carlo La Vecchia, Giovanni De Gaetano, Maria Benedetta Donati, Annamaria Colao, Alessandro Miani, Filomena Corbo, Maria Lisa Clodoveo
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-45 (2023)
Abstract Background Med-Index is a one-health front-of-pack (FOP) label, based on Mediterranean diet (MedDiet) principles, developed to summarize information about the nutritional properties and related-health benefits of any food as well as its sust
Externí odkaz:
https://doaj.org/article/60edde553aa94944a765ffa5b256937c
Publikováno v:
Biomolecules, Vol 14, Iss 8, p 1009 (2024)
When a genetic disease is characterized by the abnormal activation of normal molecular pathways and cellular events, it is illuminating to critically examine the places and times of these activities both in health and disease. Therefore, because hete
Externí odkaz:
https://doaj.org/article/01c02d04481f45f88ddfe72c06ac20a0
Autor:
Irina P. Nikishina, Svetlana V. Arsenyeva, Valeria G. Matkava, Alia N. Arefieva, Mariya I. Kaleda, Alexandr V. Smirnov, Leonid M. Blank, Mikhail M. Kostik
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-9 (2023)
Abstract Fibrodysplasia ossificans progressive (FOP) is an ultra-rare genetic disorder that is caused by a mutation in the ACVR1 gene and provokes severe heterotopic ossification. Since flares of the disease are associated with inflammation, it is as
Externí odkaz:
https://doaj.org/article/1e0a9b62261c49ddaab79a5e77ed0630
Publikováno v:
Iraqi Journal of Industrial Research, Vol 10, Iss 3 (2023)
The aim of this study is to evaluate fresh orange peels as low cost available adsorbent for removing nickel and cadmium ions from laboratory solutions and record the adsorption capacity, which represents the amount of up take per amount of fresh oran
Externí odkaz:
https://doaj.org/article/95a3ce5e3cf44d439c7e8f5a3bd7c825
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Fibrodysplasia ossificans progressiva (FOP) is an ultrarare and disabling genetic disorder of connective tissue characterized by congenital malformation of the great toes, and progressive heterotopic ossification (HO) in soft conn
Externí odkaz:
https://doaj.org/article/1acb140aaffb4553b1b214552f42f364
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-5 (2023)
Abstract Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder associated with increased immune activity and severe, progressive heterotopic ossification. We previously described a cohort of 32 patients with FOP who were either expos
Externí odkaz:
https://doaj.org/article/70cb151f9262437bb90b40fd54b216f2
Publikováno v:
Biomedicines, Vol 12, Iss 4, p 779 (2024)
Fibrodysplasia ossificans progressiva (FOP) is a debilitating genetic disorder characterized by recurrent episodes of heterotopic ossification (HO) formation in muscles, tendons, and ligaments. FOP is caused by a missense mutation in the ACVR1 gene (
Externí odkaz:
https://doaj.org/article/4dcf586db7334c53b1d8132e8f5cf964
Autor:
Qian Cong, Yingzi Yang
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 347 (2024)
Fibrodysplasia ossificans progressiva (FOP) is a rare congenital disorder characterized by abnormal bone formation due to ACVR1 gene mutations. The identification of the molecular mechanisms underlying the ectopic bone formation and expansion in FOP
Externí odkaz:
https://doaj.org/article/2072bb541e244ee8863ebf96991b11a5
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 357 (2024)
Background: Inflammation is a major driver of heterotopic ossification (HO), a condition of abnormal bone growth in a site that is not normally mineralized. Purpose of review: This review will examine recent findings on the roles of inflammation and
Externí odkaz:
https://doaj.org/article/e9936f25492d40fcb510e32b61ccdea2