About: Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report

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About: Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report Goto Sponge NotDistinct Permalink

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scientific article published on 10 December 2018

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2018 (uk) im Dezember 2018 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 2018 (ast) scientific article published on 10 December 2018 (en) 2018 թվականի դեկտեմբերի 10-ին հրատարակված գիտական հոդված (hy)
publication date	wds:Q59789607-4F93187E-B420-4C29-A88B-4C6657B6001F
publication date	2018-12-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59789607-835E102B-76AD-4C7A-99A2-443524F91683
language of work or name	English
exact match	wds:Q59789607-9681CA39-73E5-4181-A56C-228E2131B41F
exact match	https://scigraph.springernature.com/pub.10.1186/s12882-018-1152-6
cites work	wds:Q59789607-0575A04E-7ACA-4D1E-A472-6A558CC555FA wds:Q59789607-06C5C12E-FDEC-4585-A49F-89008B137EB1 wds:Q59789607-0966F6F8-D0A9-43CA-85FC-7D733772B850 wds:Q59789607-149B5B41-7118-48B6-8203-7A838D02D406 wds:Q59789607-15AC6C76-66A0-4515-BC54-DABAAC74AEA8 wds:Q59789607-199B4C7D-85F6-4164-A22F-9BC27DD2A341 wds:Q59789607-1A50D299-08C1-4E1C-9C53-8B3AC926C163 wds:Q59789607-3861FB6C-8042-4671-998E-723B291C2C27 wds:Q59789607-4521C388-E7B6-4D84-8387-1EC8832BE3FF wds:Q59789607-462FC1C5-D327-48CB-9AF2-1481DAC849BC wds:Q59789607-521FB250-BF90-4FB2-9CE2-EB964F249D20 wds:Q59789607-52A4A083-2768-4198-8B8F-1C23511859BD wds:Q59789607-562843F8-5421-4577-864E-336C90DC8506 wds:Q59789607-5CA44345-C873-4D4E-8E50-A4D7E2D9B552 wds:Q59789607-67556F9C-3EF8-4557-ACA3-F8AE00A34528 wds:Q59789607-7D7FB6E4-3435-4762-B2D3-34D1EA4E9746 wds:Q59789607-84FD6100-617F-4108-8FA1-37EC7E249E1A wds:Q59789607-8BA40001-4BDE-4896-BC60-1D491B528B93 wds:Q59789607-8CDE6BF5-B200-4C67-8092-3E7AF95062ED wds:Q59789607-A7E8E21D-9394-4484-9FEF-EC1D928B034A wds:Q59789607-AA2BF094-B010-4F41-862A-6B88AA9E8CFA wds:Q59789607-ACC2E9BF-19B7-462F-87AC-E90DE40864F9 wds:Q59789607-B80F0F2B-70B0-4C7A-87C6-637ABA9C6E46 wds:Q59789607-B9463096-2990-4D61-B66B-792A204A56CA wds:Q59789607-BF7E390B-476F-437C-865B-3D6E24D48C1B wds:Q59789607-C1E1912D-900A-411F-AEE0-9E411AA85E00 wds:Q59789607-C4D4C887-2FD7-4106-BBEC-D39924608D05 wds:Q59789607-D1563C48-63E1-4000-8F30-4B8E5E550EAA wds:Q59789607-DC9FF2E0-61EF-4148-AF32-64D57FDD2273 wds:Q59789607-EBDF76A6-3E7E-42D2-B03A-171A7E339482 wds:Q59789607-FD2D8AF1-4290-4B2E-833B-7050C79F4A8B wds:Q59789607-FD7CC357-ED8C-420B-9EAB-68108476A627
cites work	A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy Taurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseases Mass spectrometry proves under-O-glycosylation of glomerular IgA1 in IgA nephropathy Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease Genome-wide association study identifies susceptibility loci for IgA nephropathy Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens Incidence of latent mesangial IgA deposition in renal allograft donors in Japan Occurrence of mesangial IgA and IgM deposits in a control necropsy population Immunofluorescence of immunoglobulins and complement in kidneys taken at necropsy Frequency of mesangial IgA deposits in a non-selected autopsy series Regression of IgA nephropathy: a repeat biopsy study Molecular mechanisms of mitochondrial diabetes (MIDD). Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation. Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease. Mitochondrial DNA mutations in focal segmental glomerulosclerosis lesions Disappearance of mesangial IgA deposits from the kidneys of two donors after transplantation Fate of four cadaveric donor renal allografts with mesangial IgA deposits Tonsillar IgA1 as a possible source of hypoglycosylated IgA1 in the serum of IgA nephropathy patients Dimerization of a pathogenic human mitochondrial tRNA. Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group Novel lectin-independent approach to detect galactose-deficient IgA1 in IgA nephropathy Granular swollen epithelial cells: a histologic and diagnostic marker for mitochondrial nephropathy Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene. Toll-Like Receptor 9 Stimulation Induces Aberrant Expression of a Proliferation-Inducing Ligand by Tonsillar Germinal Center B Cells in IgA Nephropathy. [A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes] Pathological similarities between low birth weight-related nephropathy and nephropathy associated with mitochondrial cytopathy Disappearance of glomerular IgA deposits in childhood IgA nephropathy showing diffuse mesangial proliferation after 2 years of combination/prednisolone therapy [Study of IgA nephropathy in the transplanted kidney--sequential changes in mesangial IgA deposits found one hour post-transplantation kidney biopsies] IgA nephropathy in a girl with mitochondrial disease.
author name string	wds:Q59789607-015DE9A9-CC0B-4D04-9C09-838F86EDF624 wds:Q59789607-2927DD96-4879-47BB-BE16-4DED3F7DDB0B wds:Q59789607-5039A78D-3D62-45DA-9870-147057F9FA6E wds:Q59789607-64764390-34D1-4F0D-BB04-BDC2BA3E58AE wds:Q59789607-8C7C7179-D057-4941-A8DF-CBE0F9A2CF88 wds:Q59789607-90BE9452-806B-4A9D-9329-880AC5F24DAD wds:Q59789607-95FF7760-A402-4B4F-98EA-D0E025966F6F wds:Q59789607-A643E516-84C3-4162-80DF-55056AFFA78B wds:Q59789607-C4F04746-F764-480C-821D-D6689CD66ACB wds:Q59789607-C59C918D-2D69-4FCE-87AF-AFA36410C5B5 wds:Q59789607-CE9AB28C-2B4C-4DA1-856A-19FB064A01AA
author name string	Hiroshi Takahashi Daisuke Takahashi Takashi Yokoo Tetsuya Kawamura Yoichi Miyazaki Mai Tanaka Yutaka Yamaguchi Junichiro Kato Kazushige Hanaoka Keiji Sugai Keita Morimoto
rdfs:label	Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report (en)

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