scholarly journals The Role of Type 1 and Type 2 5′-Deiodinase in the Pathophysiology of the 3,5,3′-Triiodothyronine Toxicosis of McCune-Albright Syndrome

2008 ◽  
Vol 93 (6) ◽  
pp. 2383-2389 ◽  
Author(s):  
Francesco S. Celi ◽  
Giuseppe Coppotelli ◽  
Aaron Chidakel ◽  
Marilyn Kelly ◽  
Beth A. Brillante ◽  
...  
2003 ◽  
Vol 88 (9) ◽  
pp. 4413-4417 ◽  
Author(s):  
Michael T. Collins ◽  
Nicholas J. Sarlis ◽  
Maria J. Merino ◽  
Jason Monroe ◽  
Susan E. Crawford ◽  
...  

2021 ◽  
pp. 651-702
Author(s):  
Paul Newey

This chapter begins with genetic testing for monogenic endocrine disorders, and then goes on to define the diagnosis, treatment, and management of McCune-Albright syndrome, neurofibromatosis, von Hippel-Lindau disease, Carney complex, Cowden syndrome, and POEMS syndrome. It then goes on to the clinical features and management of MEN type 1 and MEN type 2, and MEN type 4. Inherited primary hyperparathyroidism, phaeochromocytoma-paraganglioma syndromes, and renal calculi.


2000 ◽  
Vol 143 (6) ◽  
pp. 1288-1291 ◽  
Author(s):  
J. Gonzalez‐Martin ◽  
S. Glover ◽  
S. Dixon ◽  
A. Fryer ◽  
H. Carty ◽  
...  

2019 ◽  
Vol 2 (5) ◽  
pp. 4668-4681
Author(s):  
Felipe Herbert de Oliveira Mendes ◽  
Thiago Jonathan Silva Santos ◽  
Jéssica Emanuella Rocha Paz ◽  
Ícaro Girão Evangelista ◽  
Francisco Samuel Rodrigues Carvalho ◽  
...  

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