Ken Tanikawa
Overview
Explore the profile of Ken Tanikawa including associated specialties, affiliations and a list of published articles.
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Articles
35
Citations
282
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0
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Recent Articles
1.
Kondou H, Nakano S, Mizuno T, Bessho K, Hasegawa Y, Nakazawa A, et al.
Orphanet J Rare Dis
. 2024 Feb;
19(1):57.
PMID: 38341604
Background: Progressive familial intrahepatic cholestasis type 2 (PFIC2) is an ultra-rare disease caused by mutations in the ABCB11 gene. This study aimed to understand the course of PFIC2 during the...
2.
Fukui T, Suzuki H, Tanikawa K, Takata A, Sakaguchi C, Uchida Y, et al.
Am J Gastroenterol
. 2023 Dec;
119(4):611-612.
PMID: 38084846
No abstract available.
3.
Tsuboi K, Kanbe T, Matsushima H, Ohtani Y, Tanikawa K, Kaneko M
Phys Eng Sci Med
. 2023 Sep;
46(4):1659-1666.
PMID: 37721683
The purpose of this study was to assess the optimal reconstruction parameters and the influence of tube current in extensor tendons three-dimensional computed tomography (3D CT) using deep learning reconstruction,...
4.
Tsuboi K, Osaki N, Ohtani Y, Tanikawa K, Kaneko M
Phys Eng Sci Med
. 2022 May;
45(2):637-642.
PMID: 35593991
The purpose of this study was to evaluate the effect of single-energy metal artifact reduction (SEMAR) for metal artifacts using CT images reconstructed with adaptive iterative dose reduction three dimensional...
5.
Kanno M, Suzuki M, Tanikawa K, Numakura C, Matsuzawa S, Niihori T, et al.
J Hum Genet
. 2022 Jan;
67(7):393-397.
PMID: 35087201
Paucity of interlobular bile ducts (PILBD) is a heterogeneous disorder classified into two categories, syndromic and non-syndromic bile duct paucity. Syndromic PILBD is characterized by the presence of clinical manifestations...
6.
Hashizume N, Tanaka Y, Asagiri K, Fukahori S, Ishii S, Saikusa N, et al.
Medicine (Baltimore)
. 2020 Aug;
99(31):e21332.
PMID: 32756118
Biliary atresia (BA) is a devastating cholestatic disorder of infants that presents during the first several months after birth due to an idiopathic obstruction to the bile flow. Without prompt...
7.
Shimura M, Kuranobu N, Ogawa-Tominaga M, Akiyama N, Sugiyama Y, Ebihara T, et al.
Orphanet J Rare Dis
. 2020 Jul;
15(1):169.
PMID: 32703289
Background: Hepatocerebral mitochondrial DNA depletion syndrome (MTDPS) is a disease caused by defects in mitochondrial DNA maintenance and leads to liver failure and neurological complications during infancy. Liver transplantation (LT)...
8.
Zen Y, Kondou H, Nakazawa A, Tanikawa K, Hasegawa Y, Bessho K, et al.
Hepatol Res
. 2020 Feb;
50(6):754-762.
PMID: 32073700
Aim: Bile salt export pump (BSEP) deficiency manifests a form of progressive intrahepatic cholestasis. This study aimed to establish a scoring system of liver histology for the uncommon genetic condition....
9.
Nakano S, Osaka S, Sabu Y, Minowa K, Hirai S, Kondou H, et al.
Sci Rep
. 2019 Nov;
9(1):17075.
PMID: 31745229
Progressive familial intrahepatic cholestasis (PFIC), a rare inherited disorder, progresses to liver failure in childhood. We have shown that sodium 4-phenylbutyrate (NaPB), a drug approved for urea cycle disorders (UCDs),...
10.
Watanabe J, Kai K, Tanikawa K, Hiraki M, Mizukami N, Aishima S, et al.
Diagn Pathol
. 2019 Jul;
14(1):84.
PMID: 31351495
Background: CRTC1-MAML2 fusion is often detected in low- or intermediate-grade salivary mucoepidermoid carcinoma (MEC), and it is associated with a favorable clinical course. Primary MEC of the liver is an...