Detalhe da pesquisa
1.
Predictors of Recurrence after Catheter Ablation of Paroxysmal Atrial Fibrillation in Different Follow-Up Periods.
Medicina (Kaunas)
; 56(9)2020 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32932837
2.
A Single Amino Acid Mutation Converts (R)-5-Diphosphomevalonate Decarboxylase into a Kinase.
J Biol Chem
; 292(6): 2457-2469, 2017 02 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28003359
3.
Electrophysiological relation between the superior vena cava and right superior pulmonary vein in patients with paroxysmal atrial fibrillation.
J Cardiovasc Electrophysiol
; 28(10): 1117-1126, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28675511
4.
In Vivo Formation of the Protein Disulfide Bond That Enhances the Thermostability of Diphosphomevalonate Decarboxylase, an Intracellular Enzyme from the Hyperthermophilic Archaeon Sulfolobus solfataricus.
J Bacteriol
; 197(21): 3463-71, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26303832
5.
(R)-mevalonate 3-phosphate is an intermediate of the mevalonate pathway in Thermoplasma acidophilum.
J Biol Chem
; 289(23): 15957-67, 2014 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24755225
6.
Prognosis of myocardial infarction with left ventricular dysfunction in the coronary revascularization era.Subanalysis of the Japanese Coronary Artery Disease (JCAD) Study.
Circ J
; 78(10): 2483-91, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25143319
7.
Biochemical staging of the chronic hepatic lesions of Wilson disease.
Nagoya J Med Sci
; 76(1-2): 139-48, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25130000
8.
Immediate pharmacotherapy intensification after cardiac resynchronization therapy: incidence, characteristics, and impact.
ESC Heart Fail
; 2024 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38467476
9.
Various copper and iron overload patterns in the livers of patients with Wilson disease and idiopathic copper toxicosis.
Med Mol Morphol
; 46(3): 133-40, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23338780
10.
Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.
Blood Cells Mol Dis
; 48(3): 179-82, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22297252
11.
Clinicopathological study of Japanese patients with genetic iron overload syndromes.
Pathol Int
; 62(9): 612-8, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22924847
12.
Liver structures of a patient with idiopathic copper toxicosis.
Med Mol Morphol
; 45(2): 105-9, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718296
13.
Preliminary study of spontaneous hepatitis in Long-Evans Cinnamon rats: a blood exchange may improve fetal hepatitis.
Nagoya J Med Sci
; 72(3-4): 173-7, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20942273
14.
Increase in P-glycoprotein accompanied by activation of protein kinase Calpha and NF-kappaB p65 in the livers of rats with streptozotocin-induced diabetes.
Biochim Biophys Acta
; 1782(5): 355-60, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18346469
15.
Special stain and X-ray probe microanalysis of livers with Wilson disease.
Hepatol Res
; 39(6): 563-8, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19254344
16.
Tonsillectomy plus steroid pulse therapy is the most effective treatment in adult patients with C-Grade I IgA nephropathy, and the weight of the extracted palatine tonsils and Yamamoto scale have no significant correlation with the effects of this treatment.
Auris Nasus Larynx
; 46(5): 764-771, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30665673
17.
Noninvasive Mapping of Premature Ventricular Contractions by Merging Magnetocardiography and Computed Tomography.
JACC Clin Electrophysiol
; 5(10): 1144-1157, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31648739
18.
Iron overload patients with unknown etiology from national survey in Japan.
Int J Hematol
; 105(3): 353-360, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27848180
19.
Hemojuvelin hemochromatosis receiving iron chelation therapy with deferasirox: improvement of liver disease activity, cardiac and hematological function.
Eur J Haematol
; 87(5): 467-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21848699
20.
PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
Int J Hematol
; 104(1): 125-9, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26971963