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Quoted phrase not found in phrase index: "Nephrotic syndrome, type 21"
Page 1
Glomerulonephritis Histopathological Pattern Change.
AlYousef A, AlSahow A, AlHelal B, Alqallaf A, Abdallah E, Abdellatif M, Nawar H, Elmahalawy R. AlYousef A, et al. BMC Nephrol. 2020 May 18;21(1):186. doi: 10.1186/s12882-020-01836-3. BMC Nephrol. 2020. PMID: 32423387 Free PMC article.
The indications for kidney biopsy were categorized into six clinical syndromes: nephrotic syndrome, sub-nephrotic proteinuria, nephrotic syndrome plus acute kidney injury (AKI), sub-nephrotic proteinuria plus AKI, isolated hematuria, and …
The indications for kidney biopsy were categorized into six clinical syndromes: nephrotic syndrome, sub-nephrotic prote …
Childhood nephrotic syndrome in tropical Africa: then and now.
Olowu WA, Ademola A, Ajite AB, Saad YM. Olowu WA, et al. Paediatr Int Child Health. 2017 Nov;37(4):259-268. doi: 10.1080/20469047.2017.1374002. Epub 2017 Sep 26. Paediatr Int Child Health. 2017. PMID: 28949280 Review.
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic syndrome (NS) in tropical Africa (TpAfr). In the 1960s to 1980s, corticosteroid-resistant non-minimal change disease (nMCD) includ …
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic …
Rationale and design of the Japanese Biomarkers in Nephrotic Syndrome (J-MARINE) study.
Kurasawa S, Kato S, Ozeki T, Akiyama S, Ishimoto T, Mizuno M, Tsuboi N, Kato N, Kosugi T, Maruyama S; J-MARINE collaborators. Kurasawa S, et al. Clin Exp Nephrol. 2024 May;28(5):431-439. doi: 10.1007/s10157-023-02449-4. Epub 2024 Jan 25. Clin Exp Nephrol. 2024. PMID: 38267800
INTRODUCTION: Disease subtyping and monitoring are essential for the management of nephrotic syndrome (NS). Although various biomarkers for NS have been reported, their clinical efficacy has not been comprehensively validated in adult Japanese patients. METHODS: The …
INTRODUCTION: Disease subtyping and monitoring are essential for the management of nephrotic syndrome (NS). Although various b …
Sphingosine phosphate lyase insufficiency syndrome: a systematic review.
Pournasiri Z, Madani A, Nazarpack F, Sayer JA, Chavoshzadeh Z, Nili F, Tran P, Saba JD, Jamee M. Pournasiri Z, et al. World J Pediatr. 2023 May;19(5):425-437. doi: 10.1007/s12519-022-00615-4. Epub 2022 Nov 12. World J Pediatr. 2023. PMID: 36371483 Review.
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused by biallelic mutations in SGPL1. ...Kidney disorders (42, 80.8%) were mainly in the form of steroid-resistant nephrotic syndrome …
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused …
The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study.
Li LZ, Hu Y, Ai SL, Cheng L, Liu J, Morris E, Li Y, Gou SJ, Fu P. Li LZ, et al. Sci Rep. 2019 Apr 23;9(1):6421. doi: 10.1038/s41598-019-42905-4. Sci Rep. 2019. PMID: 31015507 Free PMC article.
Abnormalities of thyroid function are common in patients with nephrotic syndrome (NS). However, a limited number of studies have reported on the association between clinicopathologic features and thyroid dysfunction in patients with NS. ...After dividing thyroid dys …
Abnormalities of thyroid function are common in patients with nephrotic syndrome (NS). However, a limited number of studies ha …
The characteristics of patients with kidney light chain deposition disease concurrent with light chain amyloidosis.
Said SM, Best Rocha A, Valeri AM, Paueksakon P, Dasari S, Theis JD, Vrana JA, Obadina MO, Saghafi D, Alexander MP, Sethi S, Larsen CP, Joly F, Dispenzieri A, Bridoux F, Sirac C, Leung N, Fogo AB, McPhail ED, Nasr SH. Said SM, et al. Kidney Int. 2022 Jan;101(1):152-163. doi: 10.1016/j.kint.2021.10.019. Epub 2021 Nov 9. Kidney Int. 2022. PMID: 34767832
The type of monoclonal light chain nephropathy is thought to be largely a function of the structural and physiochemical properties of light chains; hence most affected patients have only one light chain kidney disease type. ...Proteomic analysis of amyloid and/or LC …
The type of monoclonal light chain nephropathy is thought to be largely a function of the structural and physiochemical properties of …
A PRISMA-compliant meta-analysis of MDR1 polymorphisms and idiopathic nephrotic syndrome: Susceptibility and steroid responsiveness.
Han SS, Xu YQ, Lu Y, Gu XC, Wang Y. Han SS, et al. Medicine (Baltimore). 2017 Jun;96(24):e7191. doi: 10.1097/MD.0000000000007191. Medicine (Baltimore). 2017. PMID: 28614261 Free PMC article. Review.
BACKGROUND: Studies have investigated rs1128503, rs1045642, and rs2032582 in multidrug resistance protein 1 (MDR1) for association with susceptibility to idiopathic nephrotic syndrome (INS) and steroid resistance. However, because these findings were inconsistent, w …
BACKGROUND: Studies have investigated rs1128503, rs1045642, and rs2032582 in multidrug resistance protein 1 (MDR1) for association with susc …
A cross-sectional nationwide survey of congenital and infantile nephrotic syndrome in Japan.
Hamasaki Y, Hamada R, Muramatsu M, Matsumoto S, Aya K, Ishikura K, Kaneko T, Iijima K. Hamasaki Y, et al. BMC Nephrol. 2020 Aug 24;21(1):363. doi: 10.1186/s12882-020-02010-5. BMC Nephrol. 2020. PMID: 32838745 Free PMC article.
BACKGROUND: Congenital nephrotic syndrome (CNS) and infantile nephrotic syndrome (INS) cause substantial morbidity and mortality. ...Among those with non-Finnish-type disease, 26 had no syndrome and 24 had a syndrome, of which the …
BACKGROUND: Congenital nephrotic syndrome (CNS) and infantile nephrotic syndrome (INS) cause substantial morbidi …
Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type.
Murakoshi M, Kamei K, Ogura M, Sato M, Nada T, Suzuki R, Kamae C, Nishi K, Kanamori T, Nagano C, Nozu K, Nakanishi K, Iijima K. Murakoshi M, et al. Clin Exp Nephrol. 2022 Feb;26(2):162-169. doi: 10.1007/s10157-021-02141-5. Epub 2021 Sep 28. Clin Exp Nephrol. 2022. PMID: 34581898
BACKGROUND: The management of congenital nephrotic syndrome of the Finnish type (CNF) is challenging. It is difficult to withdraw intravenous albumin infusions, resulting in long-term hospitalization. ...Intravenous albumin infusion could be withdrawn at a me …
BACKGROUND: The management of congenital nephrotic syndrome of the Finnish type (CNF) is challenging. It is difficult t …
Detection of PLA2R Autoantibodies before the Diagnosis of Membranous Nephropathy.
Burbelo PD, Joshi M, Chaturvedi A, Little DJ, Thurlow JS, Waldman M, Olson SW. Burbelo PD, et al. J Am Soc Nephrol. 2020 Jan;31(1):208-217. doi: 10.1681/ASN.2019050538. Epub 2019 Dec 16. J Am Soc Nephrol. 2020. PMID: 31843984 Free PMC article.
BACKGROUND: Circulating serum autoantibodies against the M-type phospholipase A2 receptor (PLA2R-AB) are a key biomarker in the diagnosis and monitoring of primary membranous nephropathy (MN). ...Approximately one third of the participants became seropositive within 3 mont …
BACKGROUND: Circulating serum autoantibodies against the M-type phospholipase A2 receptor (PLA2R-AB) are a key biomarker in the diagn …
94 results