Detalhe da pesquisa
1.
Prevalence and development of idiopathic normal pressure hydrocephalus: A 16-year longitudinal study in Japan.
Acta Neurol Scand
; 146(5): 680-689, 2022 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-36114711
2.
Dysphagia worsens short-term outcomes in patients with acute exacerbation of heart failure.
Heart Vessels
; 35(10): 1429-1438, 2020 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-32361847
3.
Dysphagia Hinders Hospitalized Patients with Heart Failure from Being Discharged to Home.
Tohoku J Exp Med
; 249(3): 163-171, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31723072
4.
A multi-center, prospective study on the progression rate of asymptomatic ventriculomegaly with features of idiopathic normal pressure hydrocephalus on magnetic resonance imaging to idiopathic normal pressure hydrocephalus.
J Neurol Sci
; 419: 117166, 2020 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33065495
5.
[A case of neurofibromatosis type 2 (NF2) presenting with late-onset axonal polyneuropathy].
Rinsho Shinkeigaku
; 49(7): 419-23, 2009 Jul.
Artigo
Japonês
| MEDLINE | ID: mdl-19715170
6.
Cognitive impairment, brain ischemia and shorter telomeres are predictors of mortality in the Japanese elderly: A 13-year prospective community-based study.
J Neurol Sci
; 397: 129-134, 2019 02 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30616055
7.
Tooth Loss-associated Cognitive Impairment in the Elderly: A Community-based Study in Japan.
Intern Med
; 58(10): 1411-1416, 2019 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30626824
8.
Cerebral small vessel disease and chronic kidney disease (CKD): results of a cross-sectional study in community-based Japanese elderly.
J Neurol Sci
; 272(1-2): 36-42, 2008 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18541269
9.
Cognitive Dysfunction and Malnutrition Are Independent Predictor of Dysphagia in Patients with Acute Exacerbation of Congestive Heart Failure.
PLoS One
; 11(11): e0167326, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27898735
10.
Inflammatory Pseudotumor of the Brain Parenchyma with IgG4 Hypergammaglobulinemia.
Intern Med
; 55(14): 1911-6, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27432102
11.
A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.
PLoS One
; 11(11): e0166615, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27861535
12.
Impact of nocturnal heart rate variability on cerebral small-vessel disease progression: a longitudinal study in community-dwelling elderly Japanese.
Hypertens Res
; 38(8): 564-9, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-25787037
13.
Primary amenorrhea accompanied by adrenal adenoma: start of menarche soon after tumor resection.
Intern Med
; 41(11): 972-6, 2002 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-12487170
14.
Incidence of idiopathic normal pressure hydrocephalus (iNPH): a 10-year follow-up study of a rural community in Japan.
J Neurol Sci
; 339(1-2): 108-12, 2014 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24656600
15.
Impact of ambulatory blood pressure variability on cerebral small vessel disease progression and cognitive decline in community-based elderly Japanese.
Am J Hypertens
; 27(10): 1257-67, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-24651635
16.
Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia.
Mol Genet Metab Rep
; 1: 42-50, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-27896073
17.
Subclinical declines in the verbal fluency and motor regulation of patients with AVIM (asymptomatic ventriculomegaly with features of idiopathic NPH on MRI): a case-controlled study.
Intern Med
; 52(15): 1687-90, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-23903500
18.
Lymphomatosis cerebri with intramedullary spinal cord involvement.
Intern Med
; 52(22): 2561-5, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-24240797
19.
Changes in the subarachnoid space precede ventriculomegaly in idiopathic normal pressure hydrocephalus (iNPH).
Intern Med
; 51(13): 1751-3, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22790139
20.
An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene.
Intern Med
; 51(16): 2131-4, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22892490