Detalhe da pesquisa
1.
[Clinical diagnosis and treatment of familial medullary thyroid carcinoma caused by a p.C618Y RET proto-oncogene mutation in a Chinese pedigree].
Zhonghua Yi Xue Za Zhi
; 93(6): 440-4, 2013 Feb 05.
Artigo
Chinês
| MEDLINE | ID: mdl-23660264
2.
[The clinical patterns and RET proto-oncogene identification of pheochromocytoma in 13 multiple endocrine neoplasia type 2A pedigrees].
Zhonghua Yi Xue Za Zhi
; 93(28): 2200-4, 2013 Jul 23.
Artigo
Chinês
| MEDLINE | ID: mdl-24169328
3.
Diagnosis and treatment of primary seminoma of the prostate: A case report and review of literature.
World J Clin Cases
; 11(10): 2267-2275, 2023 Apr 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37122514
4.
Simultaneous bilateral laparoscopic cortical-sparing adrenalectomy for bilateral pheochromocytomas in multiple endocrine neoplasia type 2.
Front Surg
; 9: 1057821, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36704524
5.
The rare intracellular RET mutation p.S891A in a Chinese Han family with familial medullary thyroid carcinoma.
J Biosci
; 39(3): 505-12, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24845513
6.
p.N78S and p.R161Q germline mutations of the VHL gene are present in von Hippel-Lindau syndrome in two pedigrees.
Mol Med Rep
; 8(3): 799-805, 2013 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-23842656
7.
Genetic diagnosis of autosomal dominant polycystic kidney disease by targeted capture and next-generation sequencing: utility and limitations.
Gene
; 516(1): 93-100, 2013 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23266634
8.
RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China.
Thyroid
; 22(12): 1257-65, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-23210566
9.
RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family.
PLoS One
; 6(5): e20353, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-21655256