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Cited by in CrossRef
For: Drebber U, Andersen M, Kasper HU, Lohse P, Stolte M, Dienes HP. Severe chronic diarrhea and weight loss in cholesteryl ester storage disease: A case report. World J Gastroenterol 2005; 11(15): 2364-2366 [PMID: 15818756 DOI: 10.3748/wjg.v11.i15.2364]
URL: https://www.wjgnet.com/1007-9327/full/v11/i15/2364.htm
Number Citing Articles
1
Željko Reiner, Ornella Guardamagna, Devaki Nair, Handrean Soran, Kees Hovingh, Stefano Bertolini, Simon Jones, Marijana Ćorić, Sebastiano Calandra, John Hamilton, Terence Eagleton, Emilio Ros. Lysosomal acid lipase deficiency – An under-recognized cause of dyslipidaemia and liver dysfunctionAtherosclerosis 2014; 235(1): 21 doi: 10.1016/j.atherosclerosis.2014.04.003
2
Saber Jedidi, Kais Rtibi, Houcine Selmi, Foued Aloui, Hichem Sebai. Salvia officinalis flowers extract ameliorates liver and kidney injuries induced by simultaneous intoxication with ethanol/castor oilPhysiological Reports 2023; 11(21) doi: 10.14814/phy2.15854
3
Sandro Muntoni, Heiko Wiebusch, Marianne Jansen-Rust, Stephan Rust, Udo Seedorf, Helmut Schulte, Klaus Berger, Harald Funke, Gerd Assmann. Prevalence of Cholesteryl Ester Storage DiseaseArteriosclerosis, Thrombosis, and Vascular Biology 2007; 27(8): 1866 doi: 10.1161/ATVBAHA.107.146639
4
Pilar Giraldo, Laura López de Frutos, Jorge J Cebolla. Recommendations for overcoming challenges in the diagnosis of lysosomal acid lipase deficiencyExpert Opinion on Orphan Drugs 2022; 10(1): 11 doi: 10.1080/21678707.2022.2131393
5
Hemant Chatrath, Steven Keilin, Bashar M. Attar. Cholesterol Ester Storage Disease (CESD) Diagnosed in an Asymptomatic AdultDigestive Diseases and Sciences 2009; 54(1): 168 doi: 10.1007/s10620-008-0310-2
6
Stuart A. Scott, Benny Liu, Irina Nazarenko, Suparna Martis, Julia Kozlitina, Yao Yang, Charina Ramirez, Yumi Kasai, Tommy Hyatt, Inga Peter, Robert J. Desnick. Frequency of the cholesteryl ester storage disease commonLIPAE8SJM mutation (c.894G>A) in various racial and ethnic groupsHepatology 2013; 58(3): 958 doi: 10.1002/hep.26327
7
Lenka Ťoukálková. The rare case of boy with diagnosis LAL-DPediatrie pro praxi 2017; 18(1): 56 doi: 10.36290/ped.2017.011
8
Iraj Shahramian, Esmaeil Azimi-khatibi, Fatemeh Mahjoob, Aliyeh Sargazi, Mojtaba Delaramnasab, Ali Bazi. Histopathological Findings in Cholesteryl Ester Storage Disease: A Report of Three CasesGene, Cell and Tissue 2017; (In Press) doi: 10.5812/gct.58187
9
Sa. Muntoni, H. Wiebusch, M. Jansen-Rust, S. Rust, H. Schulte, K. Berger, L. Pisciotta, S. Bertolini, H. Funke, U. Seedorf, G. Assmann. Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrationsNutrition, Metabolism and Cardiovascular Diseases 2013; 23(8): 732 doi: 10.1016/j.numecd.2012.05.009
10
Zarife Kuloglu, Aydan Kansu, Suna Selbuz, Ayhan G. Kalaycı, Gülseren Şahin, Ceyda Tuna Kirsaclioglu, Kaan Demirören, Buket Dalgıç, Erhun Kasırga, Zerrin Önal, Ali İşlek. The Frequency of Lysosomal Acid Lipase Deficiency in Children With Unexplained Liver DiseaseJournal of Pediatric Gastroenterology and Nutrition 2019; 68(3): 371 doi: 10.1097/MPG.0000000000002224
11
T. Andrew Burrow, Kevin E. Bove, Gregory A. Grabowski. Liver Disease in Children2007; : 714 doi: 10.1017/CBO9780511547409.032
12
Tim Reynolds. Cholesteryl ester storage disease: a rare and possibly treatable cause of premature vascular disease and cirrhosisJournal of Clinical Pathology 2013; 66(11): 918 doi: 10.1136/jclinpath-2012-201302
13
C. Weiler, F. Freudenberg, J. Müller-Höcker. CholesterinesterspeicherkrankheitDer Pathologe 2009; 30(1): 65 doi: 10.1007/s00292-009-1124-5
14
Suad Siuffi-Campo, Ricardo Londoño-García, Yeinis Paola Espinosa-Herrera, Juan Camilo Pérez-Cadavid, Octavio G. Muñoz-Maya. Deficiencia de lipasa ácida lisosomal, una enfermedad subdiagnosticada. Reporte de casoHepatología 2022; : 97 doi: 10.52784/27112330.151
15
Donna L. Bernstein, Helena Hülkova, Martin G. Bialer, Robert J. Desnick. Cholesteryl ester storage disease: Review of the findings in 135 reported patients with an underdiagnosed diseaseJournal of Hepatology 2013; 58(6): 1230 doi: 10.1016/j.jhep.2013.02.014
16
Amal Aqul, Adam M. Lopez, Kenneth S. Posey, Anna M. Taylor, Joyce J. Repa, Dennis K. Burns, Stephen D. Turley. Hepatic entrapment of esterified cholesterol drives continual expansion of whole body sterol pool in lysosomal acid lipase-deficient miceAmerican Journal of Physiology-Gastrointestinal and Liver Physiology 2014; 307(8): G836 doi: 10.1152/ajpgi.00243.2014
17
Allison L. Goetsch, Dana Kimelman, Teresa K. Woodruff. Fertility Preservation and Restoration for Patients with Complex Medical Conditions2017; : 113 doi: 10.1007/978-3-319-52316-3_7
18
S. Synoracki, S. Kathemann, K. W. Schmid, H. Jastrow, H. A. Baba. Mangel an lysosomaler saurer Lipase (LAL-D)Der Pathologe 2018; 39(3): 249 doi: 10.1007/s00292-017-0400-z
19
Wolfram Haller, Khalid Sharif, Alastair JW Millar, Rachel M Brown, Patrick J McKiernan. Gallbladder Dysfunction in Cholesterol Ester Storage DiseaseJournal of Pediatric Gastroenterology and Nutrition 2010; 50(5): 555 doi: 10.1097/MPG.0b013e31819f659b
20
Bryan G. Winchester. Genetic Disorders and the Fetus2009; : 445 doi: 10.1002/9781444314342.ch12