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المؤلفDe Carvalho, Luciana Martins
المؤلفDe Sousa, Graziella Ribeiro
المؤلفMoura, Ronald
المؤلفSaggioro, Fabiano
المؤلفFacincani, Inalda
المؤلفCosta, Roberto
المؤلفKahwage, Paola Pinheiro
المؤلفDe Paula Queiroz, Rosane Gomes
المؤلفValera, Elvis Terci
المؤلفCrovella, Sergio
المؤلفSandrin-Garcia, Paula
تاريخ الإتاحة2023-06-22T09:03:57Z
تاريخ النشر2022-04-01
اسم المنشورRheumatology (United Kingdom)
المعرّفhttp://dx.doi.org/10.1093/rheumatology/keab896
الاقتباسLuciana Martins de Carvalho and others, Full-house nephropathy associated with high expression of SPATA5L1 due to a genetic pathogenic variant, Rheumatology, Volume 61, Issue 4, April 2022, Pages e84–e86, https://doi.org/10.1093/rheumatology/keab896
الرقم المعياري الدولي للكتاب14620324
معرّف المصادر الموحدhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85128489117&origin=inward
معرّف المصادر الموحدhttp://hdl.handle.net/10576/44680
الملخصDEAR EDITOR, Non-lupus full-house nephropathy is a diagnostic challenge of yet unknown aetiology that does not satisfy criteria for SLE classification . Spermatogenesis-associated protein 5-like protein 1 (SPATA5L1) is ubiquitously expressed in kidney and other tissues and has been previously associated with renal failure and chronic kidney disease (CKD) . We describe a non-lupus full-house nephropathy case showing high SPATA5L1 protein expression in the kidney and other tissues due to a pathogenic missense genetic variant. The study was approved by the Clinical Hospital of the Ribeirão Preto Medical School Research Ethics Committee (process number 3.454.601/2019), and written informed consent was obtained from the parents.
اللغةen
الناشرOxford University Press
الموضوعSPATA5L1
non-lupus full-house
العنوانFull-house nephropathy associated with high expression of SPATA5L1 due to a genetic pathogenic variant
النوعArticle
الصفحاتe84-e86
رقم العدد4
رقم المجلد61
ESSN1462-0332
dc.accessType Abstract Only


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