1 ilies, including one with isolated inherited cardiac myxomas.

2 novel heart-hand syndrome involving familial cardiac myxomas and distal arthrogryposis and demonstrat

3                 A large family with familial cardiac myxomas and the trismus-pseudocamptodactyly synd

4 s will facilitate diagnosis and treatment of cardiac myxomas and will foster new concepts in regulati

5                                    Syndromic cardiac myxomas are associated with spotty pigmentation

6                                              Cardiac myxomas are benign mesenchymal tumors that can p

7 ost common adult cardiac tumor, and familial cardiac myxomas are now appreciated to be caused by muta

8 umor syndrome Carney complex, which includes cardiac myxomas as one of its cardinal features.

9                                 Resection of cardiac myxomas, chemotherapy, radiotherapy, coil emboli

10                                     Skin and cardiac myxomas, Cushing syndrome, and acromegaly were p

11  excellent long-term survival; patients with cardiac myxomas have survival characteristics that are n

12 njunctival lesions; and its association with cardiac myxoma, highlights the need for cardiac investig

13   During the study period, we identified 112 cardiac myxomas in the pathology database and 142 in the

14                                     Familial cardiac myxomas occur in the hereditary syndrome Carney

15                  Although we did not observe cardiac myxomas or altered pigmentation in prkar1a(+/-)

16 nonymous MYH8 polymorphisms in patients with cardiac myxoma syndromes but without arthrogryposis.

17 precede vascular embolic events secondary to cardiac myxoma, thus early diagnosis of conjunctival myx