Detalhe da pesquisa
1.
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencing.
Clin Genet
; 100(1): 40-50, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33644862
2.
Clinicopathological effect of PLAG1 fusion genes in pleomorphic adenoma and carcinoma ex pleomorphic adenoma with special emphasis on histological features.
Histopathology
; 74(3): 514-525, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30307055
3.
A case of combined small cell lung carcinoma with unique morphology: Investigation of tumorigenesis.
Pathol Int
; 68(11): 618-623, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30311995
4.
Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism.
J Hum Genet
; 61(9): 839-42, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27225848
5.
[Recurrent posterior reversible encephalopathy due to vasospasm and cerebral hypoperfusionin in acute leukemia: a case report].
No To Hattatsu
; 47(6): 449-53, 2015 Nov.
Artigo
em Japonês
| MEDLINE | ID: mdl-26717647
6.
Germ Cell Neoplasia in Situ Recognized Incidentally with Complaining of Discomfort in the Right Testis: A Case Report.
Juntendo Iji Zasshi
; 69(5): 395-399, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38845730
7.
EGFR Protein Expression Relates with Tumor Histology, Methylation Status of EGFR and HPV16 E6 Viral Load in Oropharyngeal Carcinoma.
Head Neck Pathol
; 15(3): 743-756, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33428063
8.
OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation.
Front Cell Dev Biol
; 9: 631428, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33748114
9.
Identification of CTNNB1-PLAG1 gene rearrangement in a patient with pulmonary pleomorphic adenoma.
Virchows Arch
; 477(5): 739-742, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307573
10.
Pulmonary Intravascular Large B-cell Lymphoma (IVLBCL) Disguised as an Asthma Exacerbation in a Patient with Asthma.
Intern Med
; 56(14): 1885-1891, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28717087
11.
Disorganized Steroidogenesis in Adrenocortical Carcinoma, a Case Study.
Endocr Pathol
; 28(1): 27-35, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27430645
12.
Novel RAB3GAP1 compound heterozygous mutations in Japanese siblings with Warburg Micro syndrome.
Brain Dev
; 38(3): 337-40, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26421802
13.
In Japanese patients with papillary thyroid carcinoma, TERT promoter mutation is associated with poor prognosis, in contrast to BRAF V600E mutation.
Virchows Arch
; 469(6): 687-696, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27718012
14.
A case of primary spindle cell variant of embryonal rhabdomyosarcoma of the prostate.
Int J Clin Exp Pathol
; 7(8): 5181-5, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25197394
15.
IgG3 subclass-positive primary thymic MALT lymphoma without trisomy 3 and trisomy 18: report of a case and review of literature.
Int J Clin Exp Pathol
; 7(12): 8980-7, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25674276
16.
A case of myxoid liposarcoma of the breast.
Int J Clin Exp Pathol
; 6(7): 1432-6, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23826427