Results 31 to 40 of about 37,209 (255)

Update on the management of colchicine resistant Familial Mediterranean Fever (FMF)

Orphanet Journal of Rare Diseases, 2019
BackgroundFamilial Mediterranean Fever (FMF), an autoinflammatory disease, is characterized by self-limited inflammatory attacks of fever and polyserositis along with high acute phase response.
G. El Hasbani, A. Jawad, I. Uthman
semanticscholar   +1 more source

Familial Mediterranean Fever and Transverse Myelitis: A Causal Relation?

Neurology and Therapy, 2023
Familial Mediterranean fever (FMF) is a rare autoinflammatory disorder characterized mainly by recurrent self-limited episodes of fever and polyserositis.
Ali Motahharynia, Ghazaal Alavi Tabatabaei, Reza Sarrafi, Saba Naghavi, Iman Adibi   +4 more
doaj   +1 more source

Could pentraxin-3 be a new marker for subclinical inflammation in familial Mediterranean fever? [PDF]

, 2015
Not ...
Evrengül, Harun, Karadağlı, Eda, Yüksel, Selçuk, Şenol, H.   +3 more
core   +1 more source

P01-003 – Bleeding disorder in FMF [PDF]

Pediatric Rheumatology, 2013
The most serious complication in Familial Mediterranean fever (FMF) is the development of amyloidosis, which usually determines the prognosis. Amyloid deposition can be systemic or organ-specific. The clinical features of amyloidosis are dependent on the organs involved, type of amyloidosis, rate of amyloid deposition and amount of amyloid fibrils ...
Karadag, O, Telli, T Akin, Sayinalp, N, Ertenli, I   +3 more
openaire   +2 more sources

Pair of Heavy-Exotic-Quarks at LHC [PDF]

, 2002
We study the production and signatures of heavy exotic quarks pairs at LHC in the framework of the vector singlet model (VSM), vector doublet model (VDM) and fermion-mirror-fermion (FMF) model.
Almeida F. M. L., Baer H., Buchmüller W., Cieza Montalvo J. E., Dimopoulos S., Glück M., J. E. CIEZA MONTALVO, P. P. DE QUEIROZ FILHO, Rizzo T.   +8 more
core   +3 more sources

P01-013 – Cochlear involvement in FMF [PDF]

Pediatric Rheumatology, 2013
FMF is a monogenic autoinflammatory disease with recurring episodes of fever and serositis attacks. FMF is associated with mutations in pyrin. On the other hand mutations in a molecule in the same pathway, cryopyrin, is characterized by inflammatory features involving the inner ear as well.
Ayaz, N Aktay, Keskindemirci, G, Batıoglu, A, Aydogan, G, Aldemir, E, Donmez, Z, Yigit, O, Akçay, A, Ozen, Seza   +8 more
openaire   +2 more sources

Stable salts of the hexacarbonyl chromium(I) cation and its pentacarbonyl-nitrosyl chromium(I) analogue

Nature Communications, 2019
Carbonyl complexes have been studied extensively thanks to their rich substitution and redox chemistry, but most homoleptic transition metal carbonyl complexes isolated in the condensed phase are neutral or anionic.
Jan Bohnenberger, Wolfram Feuerstein, Daniel Himmel, Michael Daub, Frank Breher, Ingo Krossing   +5 more
doaj   +1 more source

The distribution of MEFV mutations in Turkish FMF patients: multicenter study representing results of Anatolia

Turkish Journal of Medical Sciences, 2019
Background/aim The distribution of Mediterranean fever (MEFV) gene mutations in Turkish familial Mediterranean fever (FMF) patients varies according to geographic area of Turkey.
Ş. Yaşar Bilge, I. Sari, D. Solmaz, S. Şenel, H. Emmungil, L. Kılıç, S. Yılmaz Öner, F. Yıldız, S. Yılmaz, Duygu Ersözlü Bozkırlı, M. Aydın Tufan, S. Yılmaz, V. Yazısız, Y. Pehlivan, C. Beş, G. Yıldırım Çetin, Ş. Erten, Emel Gönüllü, F. Şahin, S. Akar, K. Aksu, U. Kalyoncu, H. Direşkeneli, E. Erken, B. Kısacık, M. Sayarlıoğlu, M. Çınar, T. Kaşifoğlu   +27 more
semanticscholar   +1 more source

Abstract 26 — Clinical Characteristics of Familial Mediterranean: Fever in Hemodialysis Patients

Journal of Clinical Rheumatology and Immunology, 2023
Introduction Familial Mediterranean fever (FMF) is an inherited genetic disorder characterized by recurrent episodes of fever, serositis, arthritis, and skin rash. Uncontrolled disease can lead to amyloid A disposition, nephrotic syndrome and progressive
Fatima AlKindi, Ahmad Chaaban, Mohammad Al Hakim, Abraham George, Nihal AlBashir, Mohamed Saad, Mohammed Budruddin, Imran Khan, Shamma AlNokhatha, Toqa Fahmawee, Hiba Khogali, Suhail Al-Salam, Yousef Boobes   +12 more
doaj   +1 more source

Clinical features and disease severity of Turkish FMF children carrying E148Q mutation

Journal of clinical laboratory analysis (Print), 2019
Familial Mediterranean fever (FMF) is the most common hereditary monogenic autoinflammatory disease caused by mutations in the MEFV gene. It is controversial whether E148Q alteration is an insignificant variant or a disease‐causing mutation.
F. Aydın, N. Çakar, Z. Özçakar, Nermin Uncu, Ö. Başaran, S. Özdel, E. Çelikel, A. Elhan, F. Yalçınkaya   +8 more
semanticscholar   +1 more source