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Journal of Clinical Lipidology|July 1, 2022
A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiencyTadashi Takeda, Tsubasa Ide, Daishi Okuda, et al.
Journal of Clinical Lipidology|July 2, 2022
Partial lipodystrophy, severe dyslipidaemia and insulin resistant diabetes as early signs of Werner syndromeIsis Atallah, Dominique McCormick, Jean-Marc Good, et al.
Journal of Clinical Lipidology|October 17, 2020
Cardiometabolic risk factors in siblings from a statewide screening programLee A Pyles, Christa L Lilly, Amy Joseph, et al.
Journal of Clinical Lipidology|March 21, 2020
JCL roundtable: Omega-3 fatty acids and cardiovascular outcomesVera A Bittner, Terry A Jacobson, Christie M Ballantyne, et al.
Journal of Clinical Lipidology|February 29, 2020
Intermittent chylomicronemia caused by intermittent GPIHBP1 autoantibodiesAmbika P Ashraf, Kazuya Miyashita, Katsuyuki Nakajima, et al.
Journal of Clinical Lipidology|March 30, 2020
Incorporation of genetic testing significantly increases the number of individuals diagnosed with familial hypercholesterolemiaEmily E Brown, Kathleen H Byrne, Dorothy M Davis, et al.
Journal of Clinical Lipidology|October 4, 2020
Monocyte phenotyping and management of lipoprotein X syndromeZeqin Lian, Anum Saeed, Xueying Peng, et al.
Journal of Clinical Lipidology|October 11, 2020
Involvement of a homozygous exon 6 deletion of LMF1 gene in intermittent severe hypertriglyceridemiaMarine Serveaux Dancer, Oriane Marmontel, Anne-Sophie Wozny, et al.
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