![Breakthroughs that change patients’ lives]({"type":"image" , "src" : "/sda/112393/JournalAd-TACD-Pfizer-Leaderboard.jpg"})
References
- Carlson BM. Fattens foundations of embryology. 5th ed. NewYork: McGraw-Hill Book Company; 1988.
- Chenard J, Samson M, Beaulieu M. Embryonal sinosoids in the myocardium: report of a case succesfully treated sur-gically. Can Med Assoc J 1965; 92:1356–7.
- Jenni R, Goebel N, Tartini R, Schneider J, Arbenz U, Oswald O. Persistent myocardial sinosoids of both ventricles as an isolated anomaly: echocardiographic, angiographic, and pathologic anatomical findings. Cardiovasc Intervent Radiol 1986; 9:127–31.
- Ichida F, Hamamichi Y, Miyawaki T, Ono Y, Kamiya T, Akagi T, Hamada H, Hirose 0, Isobe T, Yamada K, Kuro-tobi S, Mito H, Miyake Murakami Y, Nishi T, Shinohara M, Seguchi M, Tashiro S, Tomimatsu. Clinical features of iso-lated noncompaction of the ventricular myocardium. J Am Coll Cardiol 1999; 34: 233–40.
- Chin TK, Perloff JK, Williams RG, Jue K, Mahrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 1990; 82: 507–13.
- Ritter M, Oechslin E, Sutsch G, Attenhofer C, Schneider J, Jennie R. Isolated noncompaction of the myocardium in adults. Mayo Clin Proc 1997; 72: 26–31.
- Oechlin E, Attenhofer Jost C, Rojas J, Kaufmann P, Jenni R. Long-term follow-up of 34 adults with isolated left ventric-ular noncompaction: a distinct cardiomyopathy with poor prognosis. J Am Coll Cardiol 2000; 36: 493–500.
- Kurosaki K, Ikeda U, Fujikawa H, Katsuki T, Shimida K. Familial isolated noncompaction of the left ventricular myocardium. Cardiology 1999; 9: 69–72.
- Bleyl SB, Mumford BR, Thompson V, Carey JC, Pysher TJ, Ward K, Chin TK. Neonatal, lethal noncompaction of the ventricular myocardium is allelic with Barth syndrome. Am J Hum Genet 1997; 61: 868–72.
- Bleyl SB, Mumford BR, Brown-Harrison MC, Pagotto LT, Carey JC, Pyscher TJ, Ward K, Chin TK Xq28-linked non-compaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals. Am J Med Genet 1997; 72: 257–65.
- Bione S, D’Adamo P, Maestrini E, Gedeon AK, Bolhuis PA. A novel X-linked gene, G4.5 is responsible for Barth syn-drome. Nature Genet 1996; 12: 385–9.
- D’Adamo P, Fassone L, Gedeon A, Janssen EA, Bione S, Bolhuis PA, Barth PG, Wilson M, Haan E, Orstavik KH, Patton MA, Green AJ, Zammarchi E, Donati MA, Toniolo D. The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. Am J Hum Gen 1997; 61: 862–7.
- Boyd MT, Seward JB, Tajik AJ, Edwards WD. Frequency and location of prominent left ventricular trabeculations at autopsy in 474 normal human hearts: implications for eval-uation of mural thrombi by two-dimensional echocardiog-raphy. J Am Coll Cardiol 1987; 9: 323–6.
![Committed to improving the lives of patients with Type 2 Diabetes, Heart Failure and Chronic Kidney Disease.]({"type":"image" , "src" : "/sda/112387/JournalAd-TACD-BOEHR-MPU.jpg"})
![A bold vision to stop cardiovascular disease from being a leading cause of death.]({"type":"image" , "src" : "/sda/112402/JournalAd-amarin.jpg"})