Renal involvement, presence of amyloidosis, and genotype–phenotype relationship in pediatric patients with Familial Mediterranean fever: a single center study-Reference-Cited by-同舟云学术

Renal involvement, presence of amyloidosis, and genotype–phenotype relationship in pediatric patients with Familial Mediterranean fever: a single center study

Published:2023-02-20 Issue:4 Volume:182 Page:1911-1919
ISSN:1432-1076
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Bekis Bozkurt Hayrunnisa^ORCID,Yıldırım Sema^ORCID,Ergüven Müferet^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00431-023-04855-y.pdf

Reference32 articles.

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2. Savey L, Grateau G, Georgin-Lavialle S (2021) Familial Mediterranean fever in 2020. Nephrologie et Therapeutique 17:119–125

3. Arpacı A, Doğan S, Erdoğan HF, El Ç, Cura SE (2021) Presentation of a new mutation in FMF and evaluating the frequency of distribution of the MEFV gene mutation in our region with clinical findings. Mol Biol Rep 48(3):2025–2033

4. Grossman C, Kassel Y, Livneh A, Ben-Zvi I (2019) Familial Mediterranean fever (FMF) phenotype in patients homozygous to the MEFV M694V mutation. Eur J Med Genet 62(6):103532

5. Siligato R, Gembillo G, Calabrese V, Conti G, Santoro D (2021) Amyloidosis and glomerular diseases in familial mediterranean fever. Medicina (Lithuania) 57(10):1049

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