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Organization and Technical Problems of LDL-apheresis
The International Journal of Artificial Organs, 1993 The Authors consider problems related to technique and organization of LDL-Apher-esis with respect to some particular aspects. They evaluate: a) Technical complexity of procedures both in devices to use and in staff preparation; b) Length of treatment which conditions the other fields of activity; c) Problems in management treatments periodicity ...N, Scarpato, C, Falco, G, Nappi, S, Formisano +3 moreopenaire +2 more sourcesEffects of LDL apheresis on proteinuria in patients with diabetes mellitus, severe proteinuria, and dyslipidemia
Clinical and Experimental Nephrology, 2020 T. Wada, Akinori Hara, E. Muso, S. Maruyama, Sawako Kato, K. Furuichi, K. Yoshimura, T. Toyama, N. Sakai, Hiroyuki Suzuki, T. Tsukamoto, M. Miyazaki, E. Sato, M. Abe, Y. Shibagaki, I. Narita, S. Goto, Yuichi Sakamaki, H. Yokoyama, Noriko Mori, Satoshi Tanaka, Y. Yuzawa, M. Hasegawa, T. Matsubara, J. Wada, Katsuyuki Tanabe, K. Masutani, Yasuhiro Abe, K. Tsuruya, S. Fujimoto, Shuji Iwatsubo, A. Tsuda, Hitoshi Suzuki, K. Kasuno, Y. Terada, Takeshi Nakata, N. Iino, T. Sofue, H. Miyata, T. Nakano, T. Ohtake, Shuzo Kobayashi +41 moresemanticscholar +1 more sourceRecommendations for the use of LDL apheresis
Atherosclerosis, 2008 Plasma exchange has been shown to increase life-expectancy in homozygous familial hypercholesterolaemia (FH) but increasingly is being replaced by LDL apheresis. Several methods are now available for undertaking this procedure, which lowers LDL cholesterol and Lp(a) efficiently and safely when performed weekly or bi-weekly and causes only slight ...openaire +2 more sourcesClinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry).
Journal of Clinical Lipidology, 2019 M. Kayıkçıoğlu, Ozlem Kuman-Tunçel, Ş. Pırıldar, M. Yılmaz, L. Kaynar, M. Aktan, R. Durmus, C. Gökçe, A. Temizhan, O. Özcebe, T. K. Akyol, H. Okutan, S. Sag, O. Oz Gul, Z. Şalcıoğlu, M. Yenerçağ, B. Altunkeser, I. Kuku, H. Y. Yasar, E. Kurtoğlu, Melis Demir, S. Demircioğlu, Z. Pekkolay, O. Ilhan, L. Tokgozoglu +24 moresemanticscholar +1 more sourceA nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry).
Atherosclerosis, 2018 M. Kayıkçıoğlu, L. Tokgozoglu, M. Yılmaz, L. Kaynar, M. Aktan, R. Durmus, C. Gokce, A. Temizhan, O. Ozcebe, T. K. Akyol, H. Okutan, S. Sag, O. O. Gul, Z. Şalcıoğlu, M. Yenerçağ, B. Altunkeser, I. Kuku, H. Y. Yasar, E. Kurtoğlu, M. Kose, S. Demircioğlu, Z. Pekkolay, O. Ilhan +22 moresemanticscholar +1 more source