WordNet

relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
an inflammation of the kidney (同)Bright''s disease

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1. びまん性または巣状増殖性ループス腎炎の治療 therapy of diffuse or focal proliferative lupus nephritis
2. 全身性エリテマトーデスにおける腎疾患の診断および分類 diagnosis and classification of renal disease in systemic lupus erythematosus
3. 遺伝性腎炎（アルポート症候群）の遺伝学、病因、および病理 genetics pathogenesis and pathology of hereditary nephritis alport syndrome
4. 遺伝性腎炎（アルポート症候群）の臨床症状、診断、治療 clinical manifestations diagnosis and treatment of hereditary nephritis alport syndrome
5. 糸球体疾患の鑑別診断および評価 differential diagnosis and evaluation of glomerular disease

Ortiz A1, Sanchez-Niño MD2, Izquierdo MC2, Martin-Cleary C3, Garcia-Bermejo L4, Moreno JA3, Ruiz-Ortega M5, Draibe J6, Cruzado JM6, Garcia-Gonzalez MA7, Lopez-Novoa JM8, Soler MJ9, Sanz AB10; Red de Investigacion Renal (REDINREN) and Consorcio Madrileño para investigación del fracaso renal agudo (CIFRA).
European journal of pharmacology.Eur J Pharmacol.2015 Jul 15;759:205-20. doi: 10.1016/j.ejphar.2015.03.026. Epub 2015 Mar 24.
Acute kidney injury (AKI) and chronic kidney disease (CKD) are associated with decreased renal function and increased mortality risk, while the therapeutic armamentarium is unsatisfactory. The availability of adequate animal models may speed up the discovery of biomarkers for disease staging and the
PMID 25814248

Ying T1, Hill P2, Desmond M1, Agar J1, Mallett A3.
Nephrology (Carlton, Vic.).Nephrology (Carlton).2015 Jul;20(7):506-9. doi: 10.1111/nep.12447.
Fibrillary glomerulonephritis is a rare cause of glomerulonephritis characterized by non-amyloid fibrillary deposits of unknown aetiology. It is generally considered idiopathic but may be associated with secondary causes such as monoclonal gammopathy, hepatitis B and C infections, autoimmune disease
PMID 26063488

Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis.

Gregorini G1, Izzi C2, Ravani P3, Obici L4, Dallera N5, Del Barba A6, Negrinelli A1, Tardanico R7, Nardi M8, Biasi L9, Scalvini T6, Merlini G10, Scolari F5.
Kidney international.Kidney Int.2015 Jun;87(6):1223-9. doi: 10.1038/ki.2014.389. Epub 2015 Jan 7.
Apolipoprotein A-I is the main protein of high-density lipoprotein particles, and is encoded by the APOA1 gene. Several APOA1 mutations have been found, either affecting the lecithin:cholesterol acyltransferase activity, determining familial HDL deficiency, or resulting in amyloid formation with pre
PMID 25565309

Overlap Syndrome between Familial Mediterranean Fever and Tumor Necrosis Factor Receptor-Associated Periodic Syndrome in a Lupus Patient

Nonaka Fumiaki,Migita Kiyoshi,Iwasaki Keisuke,Shimizu Toshimasa,Kawakami Atsushi,Yasunami Michio,Eguchi Katsumi
The Tohoku Journal of Experimental Medicine 233(2), 73-77, 2014
… Familial Mediterranean fever (FMF) is the most common autosomal recessive hereditary autoinflammatory disease. … She had been diagnosed with lupus nephritis at 19 years old. … Her lupus nephritis was controlled by steroid treatments; …
NAID 130004460128

加賀谷真起子,高橋博之,佐藤孝平 [他],伊藤政典
西日本皮膚科 = The Nishinihon journal of dermatology 70(1), 13-18, 2008-02-01
今回，父と2人の娘に家族性に発症したHenoch-Schönlein紫斑(Henoch-Schönlein purpura: 以下HSP)を経験したので報告する。父は特別な誘因なく紫斑が出現し，経過中に紫斑病性腎炎を発症した。家族歴として2人の娘にHSPの既往があり，長女は2年前，次女は4ヵ月前に発症していた。長女は紫斑に加え腹部症状と腎炎を伴っていた。家族性HSPの報告は希有であるが，現在まで私 …
NAID 10024943128

植田秀樹,石村栄治,奥野仙二,前川きよし,出雲谷剛,金昌雄,松本直樹,福本真也,今西康雄,絵本正憲,庄司哲雄,鰐渕英機,稲葉雅章,西沢良記
日本腎臓学会誌 44(4), 420-426, 2002
… We have experienced rare cases of membranoproliferative glomerulonephritis (MPGN)-like nephritis, which was seen in siblings. … A review of the literature revealed that familial MPGN is rare, that most of the cases have urinary abnormalities at an age of less than 10 years. … and that male preponderance is seen in familial MPGN. …
NAID 130004170585