Kunihisa Kobayashi
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Explore the profile of Kunihisa Kobayashi including associated specialties, affiliations and a list of published articles.
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72
Citations
1192
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Recent Articles
1.
Hirano K, Okamura S, Sugimura K, Miyauchi H, Nakano Y, Nochioka K, et al.
Nat Cardiovasc Res
. 2025 Feb;
PMID: 39948308
Heart disease is a major global threat. Triglyceride deposit cardiomyovasculopathy (TGCV) is an emerging, noncommunicable, adult-onset heart disease, first identified in Japanese patients with heart failure (HF) requiring cardiac transplantation....
2.
Takamiya Y, Imanaga C, Abe I, Kobayashi K, Ike A, Kawamura A, et al.
Drug Discov Ther
. 2025 Jan;
18(6):336-342.
PMID: 39756883
Several sodium-glucose cotransporter 2 (SGLT2) inhibitors are known to have beneficial effects on renal function in patients with type 2 diabetes. However, the long-term effects of luseogliflozin, an SGLT2 inhibitor,...
3.
Abe I, Takeshita K, Nagata M, Fujita Y, Ochi K, Koga M, et al.
Medicine (Baltimore)
. 2023 Sep;
102(38):e34730.
PMID: 37746989
In this real-world pilot study, we evaluated the metabolic and endocrinological effects in patients with adult growth hormone deficiency (AGHD) who switched from daily growth hormone (GH) replacement therapy to...
4.
Kobayashi K, Sakata Y, Miyauchi H, Ikeda Y, Nagasawa Y, Nakajima K, et al.
Ann Nucl Cardiol
. 2023 May;
6(1):99-104.
PMID: 37123492
Triglyceride deposit cardiomyovasculopathy (TGCV) is a newly identified disease that was discovered in individuals who required cardiac transplantation in Japan in 2008. Defective intracellular lipolysis causes triglyceride (TG) accumulation in...
5.
Hara Y, Ikeda Y, Kimura H, Shimamoto S, Ishikawa M, Kobayashi K, et al.
Mol Genet Metab Rep
. 2023 Feb;
34:100960.
PMID: 36846631
Primary triglyceride deposit cardiomyovasculopathy (P-TGCV), caused by a rare genetic mutation in encoding adipose triglyceride lipase (ATGL), exhibits severe cardiomyocyte steatosis and heart failure. Here, we report the case of...
6.
Takeshita K, Abe I, Kameda W, Ishii K, Fujita Y, Nagata M, et al.
Medicine (Baltimore)
. 2022 Dec;
101(50):e32026.
PMID: 36550872
Pituitary apoplexy is an uncommon syndrome that often results in spontaneous hemorrhage or infarction of pituitary tumors or glands. We previously reported pituitary apoplexy occurred most frequently in nonfunctional pituitary...
7.
Takeshita K, Abe I, Nagata M, Ochi K, Senda Y, Koga M, et al.
Medicine (Baltimore)
. 2022 Oct;
101(41):e30597.
PMID: 36253985
Hypothalamic adrenal insufficiency (AI) is a rare but distinct type of AI. The leading cause of hypothalamic AI is a secondary side-effect of exogenous steroid intake, particularly in large amounts...
8.
Inoguchi T, Okui T, Nojiri C, Eto E, Hasuzawa N, Inoguchi Y, et al.
Sci Rep
. 2022 Jul;
12(1):12482.
PMID: 35864124
This study aimed to develop a simplified model for predicting end-stage kidney disease (ESKD) in patients with diabetes. The cohort included 2549 individuals who were followed up at Kyushu University...
9.
Eto E, Maeda Y, Sonoda N, Nakashima N, Kobayashi K, Takayanagi R, et al.
PLoS One
. 2022 Jul;
17(7):e0271179.
PMID: 35819962
Objective: Previous reports have demonstrated the association of serum bilirubin levels with the progression of diabetic nephropathy. The objective of this study is to assess the association of basal bilirubin...
10.
Abe I, Tanaka T, Ohe K, Fujii H, Nagata M, Ochi K, et al.
J Endocr Soc
. 2022 May;
6(6):bvac068.
PMID: 35592512
Context: Mutations in the gene, also well-known as the gene, are known to cause congenital adrenal hypoplasia associated with hypogonadotropic hypogonadism. The abnormal NR0B1 protein fails to suppress the transcription...