Detalhe da pesquisa
1.
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.
Am J Hum Genet
; 104(4): 651-664, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30929736
2.
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas.
Am J Hum Genet
; 104(5): 1008-1010, 2019 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31051110
3.
Clear cell thyroid carcinoma in a patient with clear cell renal cell carcinoma: Not as clear as it seems.
Cytopathology
; 32(4): 541-544, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33848035
4.
Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma.
Front Endocrinol (Lausanne)
; 13: 1070074, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36760809
5.
Next-generation panel sequencing identifies NF1 germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1.
Eur J Endocrinol
; 178(2): K1-K9, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29158289
6.
[Adrenal ganglioneuroma: clinical and surgical dilemma concerning an incidental finding]. / Ganglioneuroma adrenal: dilema clínico-quirúrgico acerca de un hallazgo fortuito.
Endocrinol Nutr
; 60(10): e37-40, 2013 Dec.
Artigo
em Espanhol
| MEDLINE | ID: mdl-23831105