Browsing Centre for Endocrinology by Subject "Rare Diseases"
Now showing items 1-5 of 5
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Abstract P2043: Loss Of Full-length Mylk3 Causes Dilated Cardiomyopathy Via A Myl2-independent Mechanism
(Wolters Kluwer, 2023-08-04) -
Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism
(The Endocrine Society, 2023-05-08) -
PMON170 Treating human primary non-functioning pituitary adenoma cells with cabergoline
(The Endocrine Society, 2022-11-01) -
RF14 | PSAT120 X-Linked Central Precocious Puberty Associated with MECP2 Defects
(The Endocrine Society, 2022-11-01)