Results 21 to 30 of about 30,113 (242)

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

All-fiber fused directional coupler for highly efficient spatial mode conversion [PDF]

, 2014
We model and demonstrate a simple mode selective all-fiber coupler capable of exciting specific higher order modes in two- and few-mode fibres with high efficiency and purity. The coupler is based on inter-modally phase-matching the propagation constants
Brambilla, Gilberto, Ismaeel, Rand, Jung, Yongmin, Lee, Timothy, Oduro, Bernard   +4 more
core   +1 more source

A Negative Correlation Between MEFV Mutations and Allergic Diseases

Journal of Pediatric Research, 2022
Aim:Atopy is associated with a genetic predisposition to develop allergic diseases such as allergic rhinitis, asthma, and atopic dermatitis. In this study, we aimed to compare the prevalence of Familial Mediterranean Fever (FMF) mutations in asthma and ...
Malik Ejder Yıldırım, Hande Küçük Kurtulgan, Hasan Kılıçgün, Fatma Duksal   +3 more
doaj   +1 more source

Bulk inhomogeneous phases of anisotropic particles: A fundamental measure functional study of the restricted orientations model [PDF]

, 2004
The phase diagram of prolate and oblate particles in the restricted orientations approximation (Zwanzig model) is calculated. Transitions to different inhomogeneous phases (smectic, columnar, oriented, or plastic solid) are studied through minimization ...
B. G. Moore, D. Frenkel, D. Frenkel, F. van Swol, G. Cinacchi, G. Rickayzen, H. Graf, L. Harnau, L. Onsager, P. Tarazona, Y. Martínez-Ratón, Yuri Martínez-Ratón   +11 more
core   +4 more sources

Evaluation of changes in liver functions during and after FMF attacks [PDF]

African Journal of Gastroenterology and Hepatology
Background: FMF is a recessive genetic condition associated with missense and nonsense mutations in the MEFV gene, located on the short arm of chromosome 16. The serous tissue of numerous organs is the primary target of FMF.
Ahmed Mohsen, Mohamed Abdrabu, Marwa Abdou, Ali Ramadan   +3 more
doaj   +1 more source

A Transcriptional Map of the FMF Region

Genomics, 1998
Familial Mediterranean fever (FMF) is a recessively inherited disorder characterized by attacks of fever and serositis, which affects primarily non-Ashkenazi Jews, Armenians, Turks, and Arabs. We present here a transcriptional map covering the FMF locus that we constructed in the course of the positional cloning of the gene responsible for this disease.
A, Bernot, R, Heilig, C, Clepet, N, Smaoui, C, Da Silva, J L, Petit, C, Devaud, N, Chiannilkulchai, C, Fizames, D, Samson, C, Cruaud, C, Caloustian, G, Gyapay, M, Delpech, J, Weissenbach   +14 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

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

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

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