Detalhe da pesquisa
1.
A novel biosensor with high signal-to-noise ratio for real-time measurement of dopamine levels in vivo.
J Neurosci Res
; 96(5): 817-827, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29090830
2.
Erythema multiforme minor during sublingual immunotherapy.
Pediatr Int
; 63(3): 348-349, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33650188
3.
Na(+)-K(+)-2Cl(-) cotransporter-mediated fluid secretion increases under hypotonic osmolarity in the mouse submandibular salivary gland.
Am J Physiol Renal Physiol
; 306(10): F1155-60, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24623142
4.
Endothelial nitric oxide synthase plays a main role in producing nitric oxide in the superacute phase of hepatic ischemia prior to the upregulation of inducible nitric oxide synthase.
J Surg Res
; 183(2): 742-51, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23485075
5.
Levodopa-Carbidopa Intestinal Gel Injection for Patient with Severe Parkinson's Disease Followed by Total Hip Arthroplasty: A Case Report and Literature Review.
Orthop Surg
; 15(11): 2993-2999, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37712322
6.
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.
J Hum Genet
; 55(4): 244-7, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20339384
7.
A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images - A first case of CLCN2-related leukoencephalopathy in Japan.
Brain Dev
; 41(1): 101-105, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30077506
8.
The first report of Japanese patients with asparagine synthetase deficiency.
Brain Dev
; 39(3): 236-242, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27743885
9.
MR imaging and 1H-MR spectroscopy of a case of van der Knaap disease.
Brain Dev
; 28(7): 466-9, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16504440
10.
Agenesis of the gallbladder with hypoplastic cystic duct diagnosed at laparoscopy.
Surg Laparosc Endosc Percutan Tech
; 16(4): 251-4, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16921307
11.
Serial MR imaging and 1H-MR spectroscopy of unidentified bright objects in a case of neurofibromatosis type 1.
Brain Dev
; 27(8): 595-7, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15878248
12.
Postobstructive pulmonary edema that developed immediately after the removal of an endobronchial foreign body.
Intern Med
; 54(5): 497-502, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25758077
13.
Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phase.
Brain Dev
; 37(5): 471-7, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25174548
14.
A case of a teenage boy with eosinophilic gastroenteritis with esophageal involvement developing a hemorrhagic duodenal ulcer.
Clin J Gastroenterol
; 8(4): 179-85, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26037474
15.
Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding.
JIMD Rep
; 21: 115-22, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25665839
16.
Laparoscopic treatment using an argon beam coagulator for nonparasitic liver cysts.
Am J Surg
; 185(3): 273-7, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12620570
17.
MR imaging and 1H-MR spectroscopy in a case of cerebral infarction with transient cerebral arteriopathy.
Brain Dev
; 26(8): 535-8, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15533656
18.
MR imaging and 1H-MR spectroscopy in a case of juvenile Alexander disease.
Brain Dev
; 24(7): 723-6, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12427522
19.
Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.
Brain Dev
; 25(2): 116-21, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12581808
20.
Postoperative atypical hemolytic uremic syndrome associated with complement c3 mutation.
Case Rep Nephrol
; 2014: 784943, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25431709