TY - JOUR AU - Liu, L. AU - Brown, D. AU - McKee, M. AU - Lebrasseur, N. K. AU - Yang, D. AU - Albrecht, K. H. PY - 2008 DA - 2008// TI - Deletion of Cavin/PTRF causes global loss of caveolae, dyslipidemia, and glucose intolerance JO - Cell Metab VL - 8 UR - https://doi.org/10.1016/j.cmet.2008.07.008 DO - 10.1016/j.cmet.2008.07.008 ID - Liu2008 ER - TY - JOUR AU - Hill, M. M. AU - Bastiani, M. AU - Luetterforst, R. AU - Kirkham, M. AU - Kirkham, A. AU - Nixon, S. J. PY - 2008 DA - 2008// TI - PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and function JO - Cell VL - 132 UR - https://doi.org/10.1016/j.cell.2007.11.042 DO - 10.1016/j.cell.2007.11.042 ID - Hill2008 ER - TY - JOUR AU - Song, D. W. AU - Lee, K. E. AU - Ryu, J. Y. AU - Jeon, H. AU - Kim, D. H. PY - 2015 DA - 2015// TI - The molecular interaction of heart LIM protein (HLP) with RyR2 and caveolin-3 is essential for Ca(2+)-induced Ca(2+) release in the heart JO - Biochem Biophys Res Commun VL - 463 UR - https://doi.org/10.1016/j.bbrc.2015.06.045 DO - 10.1016/j.bbrc.2015.06.045 ID - Song2015 ER - TY - JOUR AU - Hayashi, Y. K. AU - Matsuda, C. AU - Ogawa, M. AU - Goto, K. AU - Tominaga, K. AU - Mitsuhashi, S. PY - 2009 DA - 2009// TI - Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy JO - J Clin Invest VL - 119 UR - https://doi.org/10.1172/JCI38660 DO - 10.1172/JCI38660 ID - Hayashi2009 ER - TY - JOUR AU - Akinci, G. AU - Topaloglu, H. AU - Akinci, B. AU - Onay, H. AU - Karadeniz, C. AU - Ergul, Y. PY - 2016 DA - 2016// TI - Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4 JO - Eur J Med Genet VL - 59 UR - https://doi.org/10.1016/j.ejmg.2016.05.001 DO - 10.1016/j.ejmg.2016.05.001 ID - Akinci2016 ER - TY - JOUR AU - Ardissone, A. AU - Bragato, C. AU - Caffi, L. AU - Blasevich, F. AU - Maestrini, S. AU - Bianchi, M. L. PY - 2013 DA - 2013// TI - Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy JO - BMC medical genetics VL - 14 UR - https://doi.org/10.1186/1471-2350-14-89 DO - 10.1186/1471-2350-14-89 ID - Ardissone2013 ER - TY - JOUR AU - Rosenberg, H. AU - Pollock, N. AU - Schiemann, A. AU - Bulger, T. AU - Stowell, K. PY - 2015 DA - 2015// TI - Malignant hyperthermia: a review JO - Orphanet J Rare Dis VL - 10 UR - https://doi.org/10.1186/s13023-015-0310-1 DO - 10.1186/s13023-015-0310-1 ID - Rosenberg2015 ER - TY - JOUR AU - Kim, J. E. AU - Chun, H. R. PY - 2017 DA - 2017// TI - Rocuronium-induced neuromuscular block and sugammadex in pediatric patient with Duchenne muscular dystrophy: a case report JO - Medicine VL - 96 UR - https://doi.org/10.1097/MD.0000000000006456 DO - 10.1097/MD.0000000000006456 ID - Kim2017 ER - TY - JOUR AU - Shimauchi, T. AU - Yamaura, K. AU - Sugibe, S. AU - Hoka, S. PY - 2014 DA - 2014// TI - Usefulness of sugammadex in a patient with Becker muscular dystrophy and dilated cardiomyopathy JO - Acta Anaesthesiol Taiwanica : Off J Taiwan Soc Anesthesiol VL - 52 UR - https://doi.org/10.1016/j.aat.2014.02.005 DO - 10.1016/j.aat.2014.02.005 ID - Shimauchi2014 ER - TY - JOUR AU - Hedley, P. L. AU - Kanters, J. K. AU - Dembic, M. AU - Jespersen, T. AU - Skibsbye, L. AU - Aidt, F. H. PY - 2013 DA - 2013// TI - The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote JO - Circ Cardiovasc Genet VL - 6 UR - https://doi.org/10.1161/CIRCGENETICS.113.000137 DO - 10.1161/CIRCGENETICS.113.000137 ID - Hedley2013 ER - TY - JOUR AU - Schwartz, P. J. AU - Moss, A. J. AU - Vincent, G. M. AU - Crampton, R. S. PY - 1993 DA - 1993// TI - Diagnostic criteria for the long QT syndrome. An update JO - Circulation VL - 88 UR - https://doi.org/10.1161/01.CIR.88.2.782 DO - 10.1161/01.CIR.88.2.782 ID - Schwartz1993 ER -