| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1
|
Lourenço Jr., Delmar M
|
|
|
67 |
S1 |
p. 99-108
|
article
|
| 2 |
Clinical and genetic aspects of familial isolated pituitary adenomas
|
Vasilev, Vladimir
|
|
|
67 |
S1 |
p. 37-41
|
article
|
| 3 |
Diagnostic work-up of gastroenteropancreatic neuroendocrine tumors
|
Öberg, Kjell
|
|
|
67 |
S1 |
p. 109-112
|
article
|
| 4 |
Familial gigantism
|
de Herder, Wouter W.
|
|
|
67 |
S1 |
p. 29-32
|
article
|
| 5 |
Genotype-phenotype correlation in multiple endocrine neoplasia type 2
|
Raue, Friedhelm
|
|
|
67 |
S1 |
p. 69-75
|
article
|
| 6 |
Head and neck paragangliomas: clinical and molecular genetic classification
|
Offergeld, Christian
|
|
|
67 |
S1 |
p. 19-28
|
article
|
| 7 |
Kinase inhibitors for advanced medullary thyroid carcinoma
|
Schlumberger, Martin
|
|
|
67 |
S1 |
p. 125-129
|
article
|
| 8 |
MENX and MEN4
|
Pellegata, Natalia S.
|
|
|
67 |
S1 |
p. 13-18
|
article
|
| 9 |
Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2
|
Wagner, Simona M.
|
|
|
67 |
S1 |
p. 77-84
|
article
|
| 10 |
Multiple endocrine neoplasias: an overview of recent progress
|
Rocha-e-Silva, Mauricio
|
|
|
67 |
S1 |
p. 1
|
article
|
| 11 |
Multiple endocrine neoplasia: the Chilean experience
|
Diaz, René E.
|
|
|
67 |
S1 |
p. 7-11
|
article
|
| 12 |
Multiple endocrine neoplasia type 2: achievements and current challenges
|
Machens, Andreas
|
|
|
67 |
S1 |
p. 113-118
|
article
|
| 13 |
Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil
|
Toledo, Rodrigo A.
|
|
|
67 |
S1 |
p. 3-6
|
article
|
| 14 |
Over-representation of the G12S polymorphism of the SDHD gene in patients with MEN2A syndrome
|
Lendvai, Nikoletta
|
|
|
67 |
S1 |
p. 85-89
|
article
|
| 15 |
Personalized medicine: caught between hope, hype and the real world
|
Dammann, Marc
|
|
|
67 |
S1 |
p. 91-97
|
article
|
| 16 |
Pituitary tumors in patients with MEN1 syndrome
|
Syro, Luis V.
|
|
|
67 |
S1 |
p. 43-48
|
article
|
| 17 |
Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1
|
Coutinho, Flavia L.
|
|
|
67 |
S1 |
p. 169-172
|
article
|
| 18 |
Primary hyperparathyroidism in multiple endocrine neoplasia type 1: when to perform surgery?
|
Giusti, Francesca
|
|
|
67 |
S1 |
p. 141-144
|
article
|
| 19 |
RET codon 609 mutations: a contribution for better clinical managing
|
Mian, Caterina
|
|
|
67 |
S1 |
p. 33-36
|
article
|
| 20 |
RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family
|
Quedas, Elisangela P.S.
|
|
|
67 |
S1 |
p. 57-61
|
article
|
| 21 |
Retroperitoneoscopic adrenalectomy in pheochromocytoma
|
Hisano, Marcelo
|
|
|
67 |
S1 |
p. 161-167
|
article
|
| 22 |
Surgical approach in patients with hyperparathyroidism in multiple endocrine neoplasia type 1: total versus partial parathyroidectomy
|
Tonelli, Francesco
|
|
|
67 |
S1 |
p. 155-160
|
article
|
| 23 |
Surgical approach to medullary thyroid carcinoma associated with multiple endocrine neoplasia type 2
|
Tavares, Marcos R.
|
|
|
67 |
S1 |
p. 149-154
|
article
|
| 24 |
Surgical management of pancreatico-duodenal tumors in multiple endocrine neoplasia syndrome type 1
|
Åkerström, Göran
|
|
|
67 |
S1 |
p. 173-178
|
article
|
| 25 |
Surgical treatment of pancreatic endocrine tumors in multiple endocrine neoplasia type 1
|
Machado, Marcel Cerqueira Cesar
|
|
|
67 |
S1 |
p. 145-148
|
article
|
| 26 |
Temozolomide in aggressive pituitary adenomas and carcinomas
|
Ortiz, Leon D.
|
|
|
67 |
S1 |
p. 119-123
|
article
|
| 27 |
The Hirschsprung's–multiple endocrine neoplasia connection
|
Moore, Sam W.
|
|
|
67 |
S1 |
p. 63-67
|
article
|
| 28 |
Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center
|
de Menezes Montenegro, Fabio Luiz
|
|
|
67 |
S1 |
p. 131-139
|
article
|
| 29 |
Variable clinical expression in patients with a germline MEN1 disease gene mutation: clues to a genotype–phenotype correlation
|
Lips, Cornelis J.
|
|
|
67 |
S1 |
p. 49-56
|
article
|
Journal description