Suchergebnisse - "Kogai, Takahiko"

PubPharm (60)

1

Inhibition of IL-33 signaling ameliorate hepatic fibrosis with decreasing MCP-1 in a mouse model of diabetes and non-alcoholic steatohepatitis; comparison for luseogliflozin, an SGLT2 inhibitor

enthalten in: Journal of diabetes and its complications | 2024

von Wakamatsu, S. | Jojima, T. | Hashiguchi, M. | +8

2

Switching from the tablet to the powder formulation of levothyroxine corrects severe hypothyroidism in a patient with lactose intolerance

enthalten in: Endocrine journal | 2022

von Jojima, T. | Shinzawa, T. | Ohira, E. | +6

3

Symptomatic hypocalcemia after treatment for hyperthyroidism in a woman with chromosome 22q11.2 deletion syndrome complicated by Graves' disease : longitudinal changes in the number of subsets of CD4 and CD8 lymphocytes after thyroidectomy

enthalten in: Endocrine journal | 2021

von Iijima, T. | Jojima, T. | Hosonuma, S. | +5

4

Empagliflozin increases plasma levels of campesterol, a marker of cholesterol absorption, in patients with type 2 diabetes : Association with a slight increase in high-density lipoprotein cholesterol

enthalten in: International journal of cardiology | 2021

von Jojima, T. | Sakurai, S. | Wakamatsu, S. | +6

CommentIn: Int J Cardiol. 2021 May 1;330:228. - PMID 33626385

5

A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation

enthalten in: Clinical case reports | 2020

von Kishi, H. | Jojima, T. | Kogai, T. | +13

6

Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia : a case report

enthalten in: European journal of endocrinology | 2020

von Jojima, T. | Kogai, T. | Iijima, T. | +13

7

A CASE OF FAMILIAL NONAUTOIMMUNE HYPERTHYROIDISM DURING PREGNANCY

enthalten in: AACE clinical case reports | 2020

von Okazaki, Y. | Arata, N. | Umehara, N. | +7

8

A Japanese Family with DICER1 Syndrome Found in Childhood-Onset Multinodular Goitre

enthalten in: Hormone research in paediatrics | 2020

von Nagasaki, K. | Shibata, N. | Nyuzuki, H. | +5

9

A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation

enthalten in: Clinical Case Reports | 2020

von Kishi, H. | Jojima, T. | Kogai, T. | +13

10

The SGLT2 Inhibitor Canagliflozin Prevents Carcinogenesis in a Mouse Model of Diabetes and Non-Alcoholic Steatohepatitis-Related Hepatocarcinogenesis : Association with SGLT2 Expression in Hepatocellular Carcinoma

enthalten in: International journal of molecular sciences | 2019

von Jojima, T. | Wakamatsu, S. | Kase, M. | +7

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