Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sumayah Aljenedil"'
Autor:
Latifah Alothman, MD, Magdaline Zawadka, MD, Sumayah Aljenedil, MD, Mahesh Kajil, MD, David Bewick, MD, Daniel Gaudet, MD, PhD, Robert A. Hegele, MD, Eva Lonn, MD, MSc, Daniel Ngui, MD, Isabelle Ruel, PhD, Michelle Tsigoulis, RN, Narendra Singh, MD, Jacques Genest, MD, Milan Gupta, MD
Publikováno v:
CJC Open, Vol 1, Iss 4, Pp 190-197 (2019)
Background: The prevalence of heterozygous familial hypercholesterolemia (FH) is 1 of 250 in the general population and approximately 1 of 125 in patients with atherosclerotic cardiovascular disease (ASCVD), yet only a minority are diagnosed. The dia
Externí odkaz:
https://doaj.org/article/d21c8b93f44b4d7b97e95899bd149a9f
Autor:
Isabelle Ruel, Zubin Lahijanian, Daniel Gaudet, Alexandre M. Bélanger, Jacques Genest, Jean Bergeron, Alexis Baass, Etienne Khoury, Latifah Alothman, Diane Brisson, Patrick Couture, Sumayah Aljenedil, Leslie Brown
Publikováno v:
Atherosclerosis. 310:54-63
Background and aims Homozygous familial hypercholesterolemia (HoFH) is an orphan disease, most often caused by bi-allelic mutations of the LDLR gene. Patients with HoFH have elevated LDL-C levels >13 mmol/L, tendinous xanthomata and severe, premature
Autor:
Milan Gupta, Daniel Ngui, Sumayah Aljenedil, Eva Lonn, Robert A. Hegele, Narendra Singh, Mahesh Kajil, Jacques Genest, Magdaline Zawadka, David Bewick, Daniel Gaudet, Isabelle Ruel, Latifah Alothman, Michelle Tsigoulis
Publikováno v:
CJC Open, Vol 1, Iss 4, Pp 190-197 (2019)
CJC Open
CJC Open
Background: The prevalence of heterozygous familial hypercholesterolemia (FH) is 1 of 250 in the general population and approximately 1 of 125 in patients with atherosclerotic cardiovascular disease (ASCVD), yet only a minority are diagnosed. The dia
Autor:
Mélanie Henderson, Julie St-Pierre, James M. Brophy, Daniel Gaudet, Katherine M. Morrison, Milan Gupta, Tisha R. Joy, Jean Bergeron, David Bewick, Liam R. Brunham, Alexis Baass, Sophie Bernard, Isabelle Ruel, Thomas Ransom, Guillaume Paré, Glen J. Pearson, Robert A. Hegele, Gordon A. Francis, Jeannette Goguen, Jack V. Tu, Pamela M. Katz, Brian W. McCrindle, Patrick Couture, Sumayah Aljenedil, Jacques Romney, G.B. John Mancini, Paolo Raggi, Jacques Genest, Jean-Baptiste Rivière
Publikováno v:
Canadian Journal of Cardiology. 34:1553-1563
Familial hypercholesterolemia (FH) is the most common monogenic disorder causing premature atherosclerotic cardiovascular disease. It affects 1 in 250 individuals worldwide, and of the approximately 145,000 Canadians estimated to have FH, most are un
Autor:
Seohyuk Lee, Leo E. Akioyamen, Jacques Genest, Sumayah Aljenedil, Jean-Baptiste Rivière, Isabelle Ruel
Publikováno v:
European journal of preventive cardiology. 26(12)
Aims Familial hypercholesterolemia (FH) is the most common genetic disorder in medicine, with a prevalence of 1/250. Affected individuals have elevated low-density lipoprotein cholesterol (LDL-C) and an increased lifetime risk of atherosclerotic card
Autor:
Gerald F. Watts, Jean Bergeron, G.B. John Mancini, Paolo Raggi, Jack V. Tu, Robert A. Hegele, Milan Gupta, Sumayah Aljenedil, Jing Pang, Robert Dufour, Alexandre M. Bélanger, Jiri Frohlich, Patrick Couture, David Bewick, Brian W. McCrindle, Claude Gagné, Alexis Baass, Jacques Genest, James M. Brophy, Gordon A. Francis, Liam R. Brunham, Isabelle Ruel, Diane Brisson, Jean Grégoire, Zuhier Awan, Daniel Gaudet
Publikováno v:
The Canadian journal of cardiology. 34(9)
Familial hypercholesterolemia (FH) is an autosomal codominant lipoprotein disorder characterized by elevated low-density lipoprotein cholesterol (LDL-C) and high risk of premature atherosclerotic cardiovascular disease. Definitions for FH rely on com
Publikováno v:
Journal of clinical lipidology. 12(4)
Background Familial hypercholesterolemia is a genetic lipoprotein disorder characterized by elevated plasma low-density lipoprotein cholesterol level, (tendinous xanthomas, xanthelasmas, and premature arcus corneus) and early onset atherosclerotic ca
Autor:
Iman Sadri, Liam R. Brunham, Isabelle Ruel, Jean Bergeron, G.B. John Mancini, Arnold Ryomoto, Patrick Couture, Diane Brisson, Gordon A. Francis, Eric Wanneh, Robert Dufour, Robert A. Hegele, James M. Brophy, Daniel Gaudet, Sumayah Aljenedil, Alexis Baass, Émilie de Varennes, Jacques Genest, Lubomira Cermakova
Publikováno v:
Clinical chemistry. 64(2)
BACKGROUND Familial hypercholesterolemia (FH) is the most frequent genetic disorder seen clinically and is characterized by increased LDL cholesterol (LDL-C) (>95th percentile), family history of increased LDL-C, premature atherosclerotic cardiovascu
Autor:
Manal Al Kindi, Sumayah Aljenedil, Alexandre M. Bélanger, Isabelle Ruel, Jacques Genest, Soumia Senouci, David Valenti, Lojan Sivakumaran, Karl Sayegh, Zuhier Awan, Khalid Al Rasadi, Khalid Al Waili
Publikováno v:
The Canadian journal of cardiology. 33(5)
Patients with homozygous and heterozygous familial hypercholesterolemia (HeFH) develop severe aortic calcifications in an age- and gene dosage-dependent manner. The purpose of this study was to determine the rate of progression of aortic calcificatio
Publikováno v:
Journal of clinical lipidology. 11(1)
Background Estrogen, whether therapeutic or physiologic, can cause hypertriglyceridemia. Hypertriglyceridemia-induced pancreatitis is a rare complication. Cases We report 2 women who developed estrogen-associated severe hypertriglyceridemia with panc