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1.
[Clinical and genetic analysis of seven Chinese pedigrees affected with multiple endocrine neoplasia type 2A with cutaneous lichen amyloidosis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(9): 938-943, 2022 Sep 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36082561
2.
[Multiple endocrine neoplasia type 2A caused by a p.C618R RET proto-oncogene mutation in a Chinese pedigree].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(3): 348-51, 2014 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-24928018
3.
[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.
Artículo
en Zh
| MEDLINE | ID: mdl-23660264
4.
[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.
Artículo
en Zh
| MEDLINE | ID: mdl-24169328
5.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-37122514
6.
Simultaneous bilateral laparoscopic cortical-sparing adrenalectomy for bilateral pheochromocytomas in multiple endocrine neoplasia type 2.
Front Surg
; 9: 1057821, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36704524
7.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-24845513
8.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-23842656
9.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-23266634
10.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-23210566
11.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-21655256
12.
The rare intracellular RET mutation p.S891A in a Chinese Han family with familial medullary thyroid carcinoma.
J Biosci
; 2014 Jun; 39 (3): 505-512
Artículo
en Inglés
| IMSEAR | ID: sea-161959
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