Current knowledge of Japanese type 1 diabetic syndrome. - Wikidata - awgldk - TriplyDB

Current knowledge of Japanese type 1 diabetic syndrome.

Current knowledge of Japanese type 1 diabetic syndrome.

http://www.wikidata.org/entity/Q34979242

about

BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1 Diabetes mellitus: The epidemic of the century.Etiopathogenesis of insulin autoimmunity.Genetics of fulminant type 1 diabetes.Prevalence of Autoantibodies and HLA DR, DQ in Type 1 Diabetes Mellitus cblb Gene Analysis in Japanese Type 1 Diabetes with Younger Age of Onset.Latent autoimmune diabetes in adults in Asians: similarities and differences between East and West.Outcomes of One Anastomosis Gastric Bypass in 472 Diabetic Patients.Autoantibody epitopes to the smaller isoform of glutamate decarboxylase do not differ in Swedish and Japanese type 1 diabetes patients and may be associated with high-risk human leucocyte antigen class II alleles.

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Current knowledge of Japanese type 1 diabetic syndrome.

http://www.wikidata.org/entity/Q34979242

description

2002 nî lūn-bûn

@nan

2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

name

Current knowledge of Japanese type 1 diabetic syndrome.

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Current knowledge of Japanese type 1 diabetic syndrome.

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Current knowledge of Japanese type 1 diabetic syndrome.

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type

label

Current knowledge of Japanese type 1 diabetic syndrome.

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Current knowledge of Japanese type 1 diabetic syndrome.

@en

Current knowledge of Japanese type 1 diabetic syndrome.

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prefLabel

Current knowledge of Japanese type 1 diabetic syndrome.

@ast

Current knowledge of Japanese type 1 diabetic syndrome.

@en

Current knowledge of Japanese type 1 diabetic syndrome.

@nl

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P1433

Diabetes - Metabolism: Research and Reviews

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Current knowledge of Japanese type 1 diabetic syndrome.

@en

P2093

Eiji Kawasaki

http://www.w3.org/2001/XMLSchema#string

Katsumi Eguch

http://www.w3.org/2001/XMLSchema#string

Norio Abiru

http://www.w3.org/2001/XMLSchema#string

P2860

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

Vitamin D receptor initiation codon polymorphism influences genetic susceptibility to type 1 diabetes mellitus in the Japanese population

Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis

Antibodies to glutamic acid decarboxylase reveal latent autoimmune diabetes mellitus in adults with a non-insulin-dependent onset of disease

Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

Incidence of Type 1 diabetes mellitus in children aged 0-14 in Japan, 1986-1990, including an analysis for seasonality of onset and month of birth: JDS study. The Data Committee for Childhood Diabetes of the Japan Diabetes Society (JDS).

Autoantigens IA-2 and GAD in Type I (insulin-dependent) diabetes.

Mononuclear cell infiltration and its relation to the expression of major histocompatibility complex antigens and adhesion molecules in pancreas biopsy specimens from newly diagnosed insulin-dependent diabetes mellitus patients.

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357-366

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scholarly article

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10.1002/DMRR.323

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5

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18

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2002-09-01T00:00:00Z

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12397578

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