Detalhe da pesquisa
1.
Lead-free MCP to improve coincidence time resolution and reduce MCP direct interactions.
Phys Med Biol
; 66(6): 064006, 2021 03 17.
Artigo
Inglês
| MEDLINE | ID: mdl-33636710
2.
Precise analysis of the timing performance of Cherenkov-radiator-integrated MCP-PMTs: analytical deconvolution of MCP direct interactions.
Phys Med Biol
; 65(10): 10NT03, 2020 06 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32325434
3.
Coincidence time resolution of 30 ps FWHM using a pair of Cherenkov-radiator-integrated MCP-PMTs.
Phys Med Biol
; 64(7): 07LT01, 2019 03 29.
Artigo
Inglês
| MEDLINE | ID: mdl-30870825
4.
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.
Nat Genet
; 17(3): 268-9, 1997 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-9354784
5.
Chemical modifications of histidyl and tyrosyl residues of inorganic pyrophosphatase from Escherichia coli.
J Biochem
; 103(5): 766-72, 1988 May.
Artigo
Inglês
| MEDLINE | ID: mdl-2846520
6.
Non-Hodgkin's lymphoma followed by plasmacytoma, both arising in A thyroid gland with Hashimoto's disease.
Leuk Lymphoma
; 35(5-6): 613-8, 1999 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-10609800
7.
Analysis of bile acids in colon residual liquid or fecal material in patients with colorectal neoplasia and control subjects.
J Gastroenterol
; 32(3): 306-11, 1997 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-9213242
8.
Clinical significance of serum iron and ferritin in patients with colorectal cancer.
J Gastroenterol
; 29(1): 19-23, 1994 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-8199692
9.
A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3).
Laryngoscope
; 108(10): 1544-7, 1998 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-9778298
10.
Plasma and erythrocyte copper, zinc, manganese and magnesium concentrations in Wilson's disease.
Clin Neurol Neurosurg
; 88(3): 193-6, 1986.
Artigo
Inglês
| MEDLINE | ID: mdl-3780108
11.
Audiologic features of hearing loss due to the 1,555 mutation of mitochondrial DNA.
Ann Otol Rhinol Laryngol
; 106(8): 643-8, 1997 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-9270426
12.
Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.
Ann Otol Rhinol Laryngol
; 106(4): 338-42, 1997 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-9109727
13.
Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct.
Acta Otolaryngol
; 120(2): 137-41, 2000 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-11603758
14.
Cytokeratin expression patterns by one- and two-dimensional electrophoresis in pars flaccida cholesteatoma and pars tensa cholesteatoma.
Acta Otolaryngol
; 115(6): 804-10, 1995 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-8749203
15.
Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology.
Acta Otolaryngol
; 116(6): 796-8, 1996 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-8973709
16.
Assessment of magnetic resonance contrast enhancement with Gd-DTPA: comparison with the uptake of Tc-99m-DTPA.
Radiat Med
; 7(5): 209-13, 1989.
Artigo
Inglês
| MEDLINE | ID: mdl-2697892
17.
Branchial cyst of the nasopharynx: resection via the endonasal approach.
J Laryngol Otol
; 109(2): 139-41, 1995 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-7706921
18.
19.
[Audiologic evaluation in a family showing diabetes mellitus and deafness associated with a mutation in mitochondrial DNA].
Nihon Jibiinkoka Gakkai Kaiho
; 98(8): 1257-62, 1995 Aug.
Artigo
Japonês
| MEDLINE | ID: mdl-7472762
20.
[Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].
Nihon Jibiinkoka Gakkai Kaiho
; 98(7): 1104-10, 1995 Jul.
Artigo
Japonês
| MEDLINE | ID: mdl-7562231