Chylomicronaemia–current diagnosis and future therapies

Cited by (356)

Items 201–300 of 356

1. Beyond the Guidelines: Perspectives on Management of Pediatric Patients with Hypertriglyceridemia
   Charles A Gagnon, Ambika P. Ashraf · 2024 · Current Atherosclerosis Reports
2. Course of Pregnancies and Occurrence of Acute Pancreatitis in Women With Chylomicronemia
   Miriam Larouche, Jean Bergeron, Diane Brisson, Nathalie Laflamme, Noémie Audet-Verreault, Claire Sharon, Sybil Charrière, Mélanie Rama, Delphine Collin‐Chavagnac, Philippe Moulin et al. · 2025 · The Journal of Clinical Endocrinology & Metabolism
3. DNA methylation levels may contribute to severe hypertriglyceridemia in multifactorial chylomicronemia syndrome
   Simon‐Pierre Guay, Martine Paquette, Amélie Taschereau, Véronique Desgagné, Luigi Bouchard, Sophie Bernard, Alexis Wilfrid Baass · 2025 · Clinical Biochemistry
4. What can we learn about lipoprotein metabolism and coronary heart disease from studying rare variants?
   Janina M. Jeff, Gina Marie Peloso, Ron Do · 2016 · Current Opinion in Lipidology
5. Quilomicronemia familiar y quilomicronemia multifactorial
   Ovidio Muñiz-Grijalvo, José Luis Díaz-Díaz · 2021 · Clínica e Investigación en Arteriosclerosis
6. Rare LPL gene missense mutation in an infant with hypertriglyceridemia
   Yuanyuan Qin, Aiqiu Wei, Qing-Wen Shan, Xiaoying Xian, Yangyang Wu, Lin Liao, Jie Yan, Zhan-feng Lai, Faquan Lin · 2018 · Journal of Clinical Laboratory Analysis
7. Novel PPARG mutation in multiple family members with chylomicronemia
   Michele Glodowski, Shannon Christen, David R. Saxon, Robert Alexander Hegele, Robert H. Eckel · 2021 · Journal of clinical lipidology
8. Advances in diagnosis and potential therapeutic options for familial chylomicronemia syndrome
   Lane B. Benes, Eric J. Brandt, Michael H. Davidson · 2017 · Expert Opinion on Orphan Drugs
9. Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s
   Masako Ueda, Frances M. Burke, Alan Thomas Remaley, Robert Alexander Hegele, Daniel James Rader, Richard L. Dunbar · 2019 · Annals of Internal Medicine
10. Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia
    Wanee Plengpanich, Suwanna Muanpetch, Supannika Charoen, Arunrat Kiateprungvej, Weerapan Khovidhunkit · 2020 · Molecular Genetics and Metabolism Reports
11. Gene expression profiles of recurrent acute pancreatitis risk in patients with sustained chylomicronemia
    Karine Tremblay, Diane Brisson, Daniel Gaudet · 2020 · Endocrine Journal
12. Genetic assessment using whole-exome sequencing for a young hypertriglyceridemic patient with repeated acute pancreatitis
    Shingo Fujita, Hitoshi Nishizawa, Yohei Miyashita, Tasuku Imada, Takashi Yamaguchi, Takeyoshi Murano, Hideaki Bujo, Yoshihiro Asano, Junji Kozawa, Norikazu Maeda et al. · 2022 · Endocrine Journal
13. Impact of a high-fat diet on dyslipidemia and gene expression of low-density lipoprotein receptors in male rats
    Ahmed A. Hussein, Nashaat Ghalib Mustafa · 2023 · Al-mağallaẗ al-ʻirāqiyyaẗ li-l-ʻulūm al-bayṭariyyaẗ/Iraqi journal of veterinary sciences
14. High hsCRP Concentration Is Associated With Acute Pancreatitis in Multifactorial Chylomicronemia Syndrome
    Simon‐Pierre Guay, Martine Paquette, Chantal Blais, Andréanne Fortin, Sophie Bernard, Alexis Wilfrid Baass · 2024 · The Journal of Clinical Endocrinology & Metabolism
15. Significant Quality of Life Improvement Observed in a Patient With FCS Associated With a Marked Reduction in Triglycerides
    Ioanna Gouni‐Berthold · 2019 · Journal of the Endocrine Society
16. Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation
    Masako Ueda, Anna T Wolska, Frances M. Burke, Maria Escobar, Laura L. Walters, Dusanka Lalic, Robert Alexander Hegele, Alan Thomas Remaley, Daniel James Rader, Richard L. Dunbar · 2020 · Case Reports in Endocrinology
17. Lipoprotein Lipase Deficiency
    Suryakumar Balasubramanian, Pearl Aggarwal, Saurabh Sharma · 2021 · StatPearls
18. Posicionamento Brasileiro sobre Síndrome da Quilomicronemia Familiar – 2023
    Maria Cristina de Oliveira Izar, Raul Dias Santos, Marcelo Heitor Vieira Assad, Antônio Carlos Palandri Chagas, Alceu de Oliveira Toledo, Ana Cláudia Cavalcante Nogueira, Ana Cristina Carneiro Fernandes Souto, Ana Maria Lottenberg, Ana Paula Marte Chacra, Carlos Eduardo dos Santos Ferreira et al. · 2023 · Arquivos Brasileiros de Cardiologia
19. Oxidative Stress, Inflammation, and Altered Lymphocyte E-NTPDase Are Implicated in Acute Dyslipidemia in Rats: Protective Role of Arbutin
    Reem Saleh Alruhaimi, Omnia E. Hussein, Sulaiman Mohammed Alnasser, Mousa O. Germoush, Meshal Alotaibi, Emad H. M. Hassanein, Mohamed El Mohtadi, Ayman Moawad Mahmoud · 2024 · Pharmaceuticals
20. Lipoprotein Lipase Deficiency Arising in Type V Dyslipidemia
    Sho Tanaka, Takahiro Ueno, Akiko Tsunemi, Yoshihiro Nakamura, Hiroki Hill Kobayashi, Yoshinari Hatanaka, Akira Haketa, Noboru Fukuda, Masayoshi Soma, Masanori Abe · 2018 · Internal Medicine
21. Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome
    Mingying Wang, Yuantao Zhou, Xiaoli He, Chengjun Deng, Xiaoning Liu, Juan Li, Lin Zhou, Ying Li, Yu Zhang, Haifeng Liu et al. · 2021 · Clinica Chimica Acta
22. Lipoprotein and Lipid Metabolism
    Robert Alexander Hegele · 2021 · Elsevier eBooks
23. Identification and Characterization of Two Novel Compounds: Heterozygous Variants of Lipoprotein Lipase in Two Pedigrees With Type I Hyperlipoproteinemia
    Shuping Wang, Yiping Cheng, Yingzhou Shi, Wanyi Zhao, Ling Gao, Fang Li, Xiaolong Jin, Han Xiao-yan, Qiuying Sun, Guimei Li et al. · 2022 · Frontiers in Endocrinology
24. Hypertriglyceridemia may contribute to stroke and pancreatitis: A case report and review of the literature
    Mingyu Zhang, Taoyuan Yin, Feng Xia, Suhong Xia, Wangdong Zhou, Yu Zhang, Xu Han, Kai Zhao, Lina Feng, Ruonan Dong et al. · 2022 · Frontiers in Endocrinology
25. Prophylactic therapeutic plasma exchange in pregnant woman with Familial Chylomicronemia Syndrome – A case report
    Ivan Pećin, Dunja Leskovar, Marina Šabić, Dražen Perica, Nediljko Šućur, Ana Godan Hauptman, Iveta Merćep, Fran Borovečki, Vedran Premužić, Bojan Jelaković et al. · 2021 · Transfusion and Apheresis Science
26. Plasma exchange therapy for familial chylomicronemia syndrome in infant: A case report
    Lei Han, Guangfeng Qiang, Lei Yang, Rui Kou, Qiubo Li, Meiyun Xin, Ruihan Liu, Zhengjun Zhang · 2022 · Medicine
27. Chylous aqueous humor caused by hyperlipidemia: A case report and literature review
    Jing Zhao, He Zou, Jun Xiao · 2023 · Medicine
28. Severe hypertriglyceridemia. Clinical characteristics and therapeutic management
    Walter M. Masson, Emiliano Rossi, Daniel Alberto Siniawski, Juan Ignacio Damonte, Ana Halsband, Ramiro Barolo, Miguel Scaramal · 2018 · Clínica e Investigación en Arteriosclerosis (English Edition)
29. Clinical heterogeneity in monogenic chylomicronaemia
    Britt E. Heidemann, Remy H.H. Bemelmans, Adrian David Marais, Frank L.J. Visseren, Charlotte Koopal · 2022 · BMJ Case Reports
30. Case report: desensitization of hypersensitivity against the antisense oligonucleotide volanesorsen
    Rafael H. Isaac, Deyanira González Devia, Carlos Olimpo Mendivil, Edgardo Chapman · 2023 · Frontiers in Allergy
31. Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
    Ka Young Kim, You Joung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Chang Seok Ki, Yun Jeong Lee · 2024 · BMC Endocrine Disorders
32. Clinical characterization and mutation spectrum of patients with hypertriglyceridemia in a German outpatient clinic
    Frieda Bardey, Lorenz Rieck, Dominik Spira, Winfried März, Priska Binner, Stefanie K. Schwab, Marcus Edi Kleber, Magdalena Danyel, Rasmus Barkowski, Thomas Bobbert et al. · 2024 · Journal of Lipid Research
33. Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing
    Ying Liu, Zhangzhang Lan, Fang Zhao, Shuangchuan Zhang, Wenyong Zhang · 2020 · Frontiers in Genetics
34. A Case of Type V Hyperlipoproteinemia Resistant to Insulin Treatment
    Shaunak Mangeshkar, Natalia Nazarenko, Dimitrios Varrias, Michail Spanos, Paweł Borkowski, Majd Al Deen Alhuarrat, Weijia Li, Preeti Kishore, Robert T. FAILLACE · 2023 · Cureus
35. Case Report: Management of a Patient With Chylomicronemia Syndrome During Pregnancy With Medical Nutrition Therapy
    Maryam Zahedi, Golaleh Asghari, Parvin Mirmiran, Farhad Hosseinpanah · 2021 · Frontiers in Nutrition
36. Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency
    Yakun Li, Man Hu, Lin Han, Lifang Feng, Luhong Yang, Xiaoqian Chen, Tingting Du, Hui Yao, Xiaohong Chen · 2022 · Frontiers in Genetics
37. Antisense Oligonucleotides for the Treatment of Hypertriglyceridemia and Hyperlipoproteinemia(a)
    Ruth Hanßen, Ioanna Gouni‐Berthold · 2017 · Current Pharmacology Reports
38. Lipoprotein Lipase Deficiency: Diet is the Key!
    Kshitija Patil, Neerja Gupta · 2021 · The Indian Journal of Pediatrics
39. Diagnosis, Evaluation, and Management of Severe Hypertriglyceridemia
    Amrita Krishnamurthy, Edwin A. Homan, Samuel M. Kim · 2025 · Current Cardiovascular Risk Reports
40. A multidisciplinary management model for severe gestational hypertriglyceridemia: using plasmapheresis to prevent pancreatitis in pregnancy
    Xixi Zheng, Peng Xia, Cai Yue, Jinghua Xia, Yue Zhou, Liting Chen, Yingna Song, Jinsong Gao, Naishi Li, Xuemei Li et al. · 2025 · BMC Pregnancy and Childbirth
41. Long-term efficacy and safety of lomitapide in patients with familial chylomicronemia syndrome: Data from an expanded access program
    Antonina Giammanco, Laura D’Erasmo, Gabriella Iannuzzo, Davide Noto, Anna Montali, Alberto Zambon, Francesco Forte, Patrizia Suppressa, Stefano Giannini, Carlo Maria Barbagallo et al. · 2025 · Journal of clinical lipidology
42. Hypertriglyceridaemia-Associated Acute Pancreatitis: Pathophysiological Insights and Advances in Clinical Management
    Yuying Li, Xinran Zhou, Yongjian Wen, Qianzi Huang, Xinmin Yang, Rajarshi Mukherjee, Robert Sutton, Tingting Liu, Wenhao Cai, Wei Huang · 2026 · Biomedicines
43. A very rare case of chylomicronemia revealed by cerebral thrombophlebitis in a 4-month-old infant
    Ounci Es-Saad, Oussama Lamzouri, Amine Bouchlarhem, Leïla Haddar, Mohammed Aabdi, Hamza Mimouni, Kaoutar zerouati, Houssam Bkiyar, Brahim Housni · 2022 · Annals of Medicine and Surgery
44. Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: A case report and review of literature
    Yunhua Huang, Yuanyuan Qin, Lin Liao, Faquan Lin · 2022 · Clinica Chimica Acta
45. Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry
    Lan Jiang, Srushti Gangireddy, Alyson L. Dickson, Yi Xin, Chao Yan, Vivian K. Kawai, Nancy Jean Cox, MacRae F. Linton, W Wei, Christoph Stein et al. · 2024 · Journal of Lipid Research
46. Diagnosis and stabilisation of familial chylomicronemia syndrome in two infants presenting with hypertriglyceridemia‐induced acute pancreatitis
    Oliver Heath, Brooke Allender, Joel D. Smith, Elena Savva, Lucy Spencer, Elizabeth G. Bannister, Natasha J. Brown, Maureen S. Evans, Sharmila Kiss, Thomas H. Rozen et al. · 2024 · JIMD Reports
47. Familial chylomicronaemia syndrome in pregnancy – report of two cases managed with plasma exchange
    Francois Dos Santos, Shahenaz Walji, Jaimini Cegla, Sheba Jarvis, Catherine Nelson‐Piercy · 2024 · Obstetric Medicine
48. A foray into Understanding the Next Billion Search Users
    Naman Gupta, Carolyn Penstein Rosé · 2009
49. Chylomicronemia Due to the Rare Hyperlipoproteinemia Type 3 Complicated by a Circulating Monoclonal Protein
    Hiba Basheer, Beheshteh Nakhaee, Ishwarlal Jialal · 2021 · Laboratory Medicine
50. FISIOPATOLOGIA E TRATAMENTOS ATUALMENTE DISPONÍVEIS PARA DISLIPIDEMIA
    Adilson Boson Almeida, Beatriz Brígido Pontes, Luciana Netto Gioia, Vinicius Rangel · 2023 · EPITAYA eBooks
51. Novel pathogenic variant combination in LPL causing familial chylomicronemia syndrome in an Asian family and experimental validation in vitro: a case report
    Huiping Shi, Zhaoyue Wang · 2022 · Translational Pediatrics
52. Secondary causes of chylomicronemia: defining the underside of the iceberg
    Amanda J. Berberich, Robert Alexander Hegele · 2018 · Journal of Internal Medicine
53. Rapidly lowering triglyceride levels by plasma exchange in acute pancreatitis: What's the point?
    Amanda J. Berberich, Robert Alexander Hegele · 2022 · Journal of Clinical Apheresis
54. Cross-Sectional Quantitative Evaluation of a Novel Patient-Reported Outcome Measure in Familial Chylomicronemia Syndrome
    T. Michelle Brown, Montserrat Vera‐Llonch, Chisom Kanu, Asia Sikora Kessler, Aaron S. Yarlas, Sheri E. Fehnel · 2024 · Patient Related Outcome Measures
55. Severe Hypertriglyceridemia in a Patient With Metabolic Syndrome and Psoriasis on Risankizumab-Rzaa
    Isra Abdulwadood, Jose F de Melo, Robert Scheel, John P. Bois · 2024 · JCEM Case Reports
56. Severe Hypertriglyceridemia in Patients with Type 2 Diabetes Mellitus Participating in the AMD Annals Initiative
    Giuseppina Tiziana Russo, Valeria Manicardi, Alberto Rocca, Antonio Nicolucci, Annalisa Giandalia, Giuseppe Lucisano, Maria Chiara Rossi, Giusi Graziano, Paolo Di Bartolo, Salvatore De Cosmo et al. · 2024 · Metabolic Syndrome and Related Disorders
57. Current Perspectives of Diabetic Dyslipidemia and Treatment Modalities
    Gamze Akkuş · 2025 · Current Medicinal Chemistry
58. Management of dyslipidemia in adults. A consensus statement from the French Society of Endocrinology (SFE), the French-speaking Diabetes Society (SFD), the New French-speaking Atherosclerosis Society (NSFA) and the French Society of Cardiology (SFC)
    Benjamin Bouillet, Romain Boulestreau, Victor Aboyans, Sophie Béliard, Franck Boccara, Bertrand Cariou, Sybil Charrière, Philippe Moulin, Bruno L Vergès, René Valéro et al. · 2026 · Archives of cardiovascular diseases
59. Comparison of different “familial chylomicronemia syndrome” clinical diagnosis scoring systems in patients with persistent chylomicronemia
    Diane Brisson, Miriam Larouche, Nathalie Laflamme, Seyedmohammad Saadatagah, Jean Bergeron, Christie Mitchell Ballantyne, Daniel Gaudet · 2026 · Journal of clinical lipidology
60. Clinical and molecular characterization of familial chylomicronemia in Saudi patients: a retrospective study
    Abdullah A. Al-Ashwal, Manal AlHelal, Afaf Alsagheir, Areej A. G. AlFattani, Khushnooda Ramzan, Faiqa Imtiaz, Raghad Tariq Alhuthil · 2024 · Frontiers in Endocrinology
61. Familial chylomicronemia syndrome caused by 2 genetic variants in the APOA5 gene: Severe hypertriglyceridemia that complicates pregnancy
    Johnayro Gutiérrez-Restrepo, Pablo Castaño, Gregorio Fariña, Gabriela Alicia Berg, Jubby Marcela Gálvez, Juan Patricio Nogueira · 2025 · Journal of clinical lipidology
62. Patient experience with familial chylomicronemia syndrome before and after olezarsen treatment: Qualitative interviews with clinical trial participants
    Asia Sikora Kessler, T. Michelle Brown, Emily Bratlee‐Whitaker, Sheri E. Fehnel, Montserrat Vera‐Llonch, Marcello Arca, Maurizio Rocco Averna, Alexis Wilfrid Baass, Seth J. Baum, Jean Bergeron et al. · 2025 · Journal of clinical lipidology
63. A 19 year follow‐up of a woman with lipoprotein lipase deficiency treated with biliopancreatic diversion
    Gabriella Nosso, Brunella Capaldo, Sara Cocozza, Olga Vaccaro · 2015 · Clinical Case Reports
64. Lipemia poposiłkowa — problem kliniczny i potencjalne miejsce w algorytmach diagnostycznych Stanowisko polskich ekspertów
    Anna Skoczyńska, Marta Wawrzynowicz‐Syczewska, Marta Barlik-Rysa, Andrzej Danik, Jacek Różański, Krzysztof Jerzy Filipiak, Barbara Cybulska · 2020 · Folia Cardiologica
65. Insulin can be used to treat severe hypertriglyceridaemia in pregnant women without diabetes
    Aleena Shujaat Ali · 2021 · BMJ Case Reports
66. Bioinformatic Analyses of Peripheral Blood Transcriptome Identify Altered Neutrophil-Related Pathway and Different Transcriptomic Profiles for Acute Pancreatitis in Patients with and without Chylomicronemia Syndrome
    Chia-Lun Liu, Yang-Hong Dai · 2023 · Biomolecules
67. Special Patient Populations
    Daniel Gaudet · 2023 · Elsevier eBooks
68. Oligonucléotide antisens de l’apolipoprotéine C-III : nouveau traitement de certaines hypertriglycéridémies sévères
    René Valéro · 2020 · Médecine des Maladies Métaboliques
69. Chylomicrons: When you can't direct the wind, adjust the sail
    Latifah Alothman, Jacques J. Genest · 2019 · Atherosclerosis
70. Eruptive xanthomas
    Vikrant Abhay Saoji, Bhushan Madke, Jayashri Shembalkar, Kinjal Deepak Rambhia · 2024 · BMJ Case Reports
71. Carotid intima-medial thickness in patients with severe hypertriglyceridemia
    Maud Ahmad, Brooke A. Kennedy, Surim Son, Adam D. McIntyre, Julieta Lazarte, Jian Wang, Robert Alexander Hegele · 2024 · Atherosclerosis Plus
72. A qualitative study to explore the patient experience of hypertriglyceridemia-related acute pancreatitis
    Asia Sikora Kessler, Daniel Aggio, Ellen Howard, Daniel E. Soffer, Jordi Alonso, Sarah Acaster, Kate Williams · 2025 · Journal of clinical lipidology
73. Female-Specific Risk of Pancreatitis in Severe Hypertriglyceridemia: Implications for Family Planning and New Guidelines
    Mohamed Haseef, Dick C. Chan, Gerald Francis Watts · 2025 · The Journal of Clinical Endocrinology & Metabolism
74. 2025 Egyptian guidelines for the management of dyslipidemia
    Ashraf Reda, Hesham Taha, Hala Mahfouz Badran, Hazem Khamis, Sherif Kamal, Ahmed Shawky Elserafy, Muhammad Hasan Dawoud, Ahmed A. Elamragy, Ahmed Bendary, Mirna Mamdouh Shaker · 2026 · The Egyptian Heart Journal
75. Olezarsen and Beyond: Emerging Targeted Treatments for Familial Chylomicronemia Syndrome and Related Triglyceride Disorders
    N Meghashree, Kushal C B, D R Shivaraj · 2026 · Journal of Lipid and Atherosclerosis
76. Management of dyslipidemia in adults. A consensus statement from the French Society of Endocrinology (SFE), the French-speaking Diabetes Society (SFD), the New French-speaking Atherosclerosis Society (NSFA) and the French Society of Cardiology (SFC)
    Benjamin Bouillet, Romain Boulestreau, Victor Aboyans, Sophie Béliard, Franck Boccara, Bertrand Cariou, Sybil Charrière, Philippe Moulin, Bruno L Vergès, René Valéro et al. · 2026 · Diabetes & Metabolism
77. The evaluation of plozasiran for the treatment of familial chylomicronemia syndrome
    Shyann Hang, Robert Alexander Hegele · 2026 · Expert Review of Endocrinology & Metabolism
78. Autoimmune-Mediated Hypertriglyceridemia in a Young Male with Refractory Immune Thrombocytopenia: A Case Report
    Batya Green, Eran Leitersdorf, Shoshana Shpitzen, Rayan Alyan, Daniel Schurr, Aviv Talmon, Yuval Tal, Merielle Kaplan, Ram Weiss, R.Y. Durst · 2026 · Journal of Lipid Research
79. Investigated treatments for lipoprotein lipase deficiency and related metabolic disorders
    Joo-Ho Lee, Robert Alexander Hegele · 2017 · Expert Opinion on Orphan Drugs
80. Genetic Disorders of Lipoprotein Metabolism
    Alan S. Brown, Ehab G. Dababneh, Adib M. Chaus, Vadzim Chyzhyk, Victor Marinescu, Nataliya Pyslar · 2020 · Contemporary cardiology
81. Bases genéticas de las hipertrigliceridemias
    Beatriz Candás‐Estébanez, Ariadna Padró‐Miquel, Virginia Esteve-Luque · 2021 · Clínica e Investigación en Arteriosclerosis
82. Genetic Disorders of Lipoprotein Metabolism: Diagnosis and Management
    Arjen J. Cupido, Robert M. Stoekenbroek, John J.P. Kastelein · 2016 · Springer eBooks
83. Atherosclerosis
    Murray W. Huff, Katey J. Rayner · 2021 · Elsevier eBooks
84. Infantile Hyperchylomicronemia Due to A Novel GPIHBP1 Disease-Causing Variant Presenting with Milky Blood: A Rare Case Report
    Iman Marzouq, Basant Elbanna, Sabine Schröder, Kornélia Tripolszki, Aida Maria Bertoli‐Avella, Aml Mahfouz · 2023 · Jurnal Gastrohepatologi Anak Indonesia/Archives of Pediatric Gastroenterology, Hepatology, and Nutrition
85. Triglyceride Clearance in Hypertriglyceridemic Pancreatitis: Time Course and Its Implications for Management
    Sachin K. Majumdar · 2023 · Endocrine Practice
86. A Man with Primary Hyperchylomicronemia with Triglyceride Levels Exceeding 11,000 mg/dL Was Well Controlled by Pemafibrate Combined with Dietary Therapy
    Hiroyuki Ueda, Ryohei Mineo, Takuya Sugiyama, Masahiro Koseki, Yoshito Itoh, Ryuya Iwamoto, Sachiko Tamba, Koji Yamamoto, Yuya Yamada, Hisatoyo Hiraoka et al. · 2024 · Internal Medicine
87. Two Novel Mutations Associated with Familial Chylomicronemia in a Neonate
    Vikas V Jha, Girish Arora, Vinika Arora · 2024 · Newborn
88. A brief clinical genetics review: stepwise diagnostic processes of a monogenic disorder—hypertriglyceridemia
    Masako Ueda · 2024 · Translational Pediatrics
89. Genetic basis of hypertriglyceridemia
    María José Ariza Corbo, Ovidio Muñiz-Grijalvo, Agustín Blanco Echevarría, José Luis Díaz-Díaz · 2024 · Clínica e Investigación en Arteriosclerosis (English Edition)
90. DNA methylation levels are independently associated with prevalence of atherosclerotic cardiovascular disease in multifactorial chylomicronemia syndrome
    Simon‐Pierre Guay, Martine Paquette, Amélie Taschereau, Véronique Desgagné, Luigi Bouchard, Sophie Bernard, Alexis Wilfrid Baass · 2025 · Clinical Biochemistry
91. Advances in Hypercholesterolemia
    Angela Pirillo, Giuseppe Danilo Norata, Alberico Luigi Catapano · 2016 · Elsevier eBooks
92. Neues zu Relevanz und Behandlung des Chylomikronämie-Syndroms
    Gerald Klose · 2019 · CardioVasc
93. Severe Hypertriglyceridemia in the Hospitalized Patient
    Roselyn Cristelle Isidro Mateo, Om P. Ganda · 2020 · Springer eBooks
94. Síndrome de Quilomicronemia Familiar: Algoritmo Diagnóstico
    Ines Bertao Colaco, Francisco Araújo, Patrício Aguiar, Diogo Cruz, Mafalda Bourbon, João Sequeira Duarte, Manuel Teixeira Veríssimo · 2021 · Medicina Interna
95. Genetic testing in dyslipidaemia: An approach based on clinical experience
    Amanda J. Berberich, Robert Alexander Hegele · 2022 · Best Practice & Research Clinical Endocrinology & Metabolism
96. Molecular Genetics of Hypertriglyceridaemia
    Jacqueline S. Dron, Robert Alexander Hegele · 2017 · Encyclopedia of Life Sciences
97. Classification of Hyperlipidemias and Dyslipidemias
    Jesús E. Millán Núñez-Cortes, Joaquín J. Millán Pérez · 2018 · Elsevier eBooks
98. Commentary on rare dyslipidaemia paper
    Jane K. Stock · 2019 · Atherosclerosis
99. Exploring the biological function of carboxypeptidase O: analysis of expression and association with chylomicrons and lipid droplets
    Erika Bauza Nowotny · 2020
100. Fine-grained authorization for job execution in the Grid: design and implementation: Research Articles
     Katarzyna Keahey, Von Welch, Samuel J. Lang, B. Liu, S. Meder · 2004 · Middleware for Grid Computing