Detalhe da pesquisa
1.
Congenital hyperinsulinism treated by surgical resection of the hyperplastic lesion which had been preoperatively diagnosed by 18F-DOPA PET examination in Japan: a nationwide survey.
Pediatr Surg Int
; 34(10): 1093-1098, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30076450
2.
Efficacy and safety of octreotide for the treatment of congenital hyperinsulinism: a prospective, open-label clinical trial and an observational study in Japan using a nationwide registry.
Endocr J
; 64(9): 867-880, 2017 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28701683
3.
Congenital hyperinsulinism: global and Japanese perspectives.
Pediatr Int
; 56(4): 467-76, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24865345
4.
Efficacy and safety of long-term, continuous subcutaneous octreotide infusion for patients with different subtypes of KATP-channel hyperinsulinism.
Clin Endocrinol (Oxf)
; 78(6): 891-7, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23067144
5.
Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome.
Endocr J
; 60(4): 403-8, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23197114
6.
Diagnostic accuracy of [¹8F]-fluoro-L-dihydroxyphenylalanine positron emission tomography scan for persistent congenital hyperinsulinism in Japan.
Clin Endocrinol (Oxf)
; 75(3): 342-6, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21521340
7.
Focal form of congenital hyperinsulinism clearly detectable by contrast-enhanced computed tomography imaging.
Int J Pediatr Endocrinol
; 2015(1): 20, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26379717
8.
Ictal and interictal single photon emission computed tomography in a patient with benign familial infantile convulsions.
J Neuroimaging
; 12(1): 75-7, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11826605
9.
Lasting 18F-DOPA PET uptake after clinical remission of the focal form of congenital hyperinsulinism.
Horm Res Paediatr
; 76(4): 286-90, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21912073
10.
Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.
J Clin Endocrinol Metab
; 96(1): E141-5, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20943781