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Cited by in CrossRef
For: Santillán-Hernández Y, Almanza-Miranda E, Xin WW, Goss K, Vera-Loaiza A, Mora MTGDL, Piña-Aguilar RE. Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency. World J Gastroenterol 2015; 21(3): 1001-1008 [PMID: 25624737 DOI: 10.3748/wjg.v21.i3.1001]
URL: https://www.wjgnet.com/1007-9327/full/v21/i3/1001.htm
Number Citing Articles
1
Gregory A. Grabowski, Hong Du. Cholesterol2022; : 639 doi: 10.1016/B978-0-323-85857-1.00022-5
2
I. N. Zakharova, А. N. Goryaynova, I. D. Maikova, N. V. Koroid, L. P. Katasonova, O. I. Elfimova, N. E. Kuzina, E. A. Dikova. Lysosomal lipid storage diseases in children. Modern diagnostic and treatment methodsMedical Council 2016; 1(1): 128 doi: 10.21518/2079-701X-2016-1-128-135
3
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
4
R. Vázquez-Frias, J.E. García-Ortiz, P.F. Valencia-Mayoral, G.E. Castro-Narro, P.G. Medina-Bravo, Y. Santillán-Hernández, J. Flores-Calderón, R. Mehta, C.A. Arellano-Valdés, L. Carbajal-Rodríguez, J.I. Navarrete-Martínez, M.L. Urbán-Reyes, M.T. Valadez-Reyes, F. Zárate-Mondragón, A. Consuelo- Sánchez. Consenso mexicano sobre el diagnóstico de la deficiencia de lipasa ácida lisosomalRevista de Gastroenterología de México 2018; 83(1): 51 doi: 10.1016/j.rgmx.2017.08.001
5
Guillermo Angel, Andrew T. Hutchinson, Nina K. Jain, Chris D. Forbes, John Reynders. Large‐scale functionalLIPAvariant characterization to improve birth prevalence estimates of lysosomal acid lipase deficiencyHuman Mutation 2019; 40(11): 2007 doi: 10.1002/humu.23837
6
Svetlana Mikhailova, Dinara Ivanoshchuk, Olga Timoshchenko, Elena Shakhtshneider. Genes Potentially Associated with Familial HypercholesterolemiaBiomolecules 2019; 9(12): 807 doi: 10.3390/biom9120807
7
Rohit Kohli, Vlad Ratziu, Maria Isabel Fiel, Elisa Waldmann, Don P. Wilson, Manisha Balwani. Initial assessment and ongoing monitoring of lysosomal acid lipase deficiency in children and adults: Consensus recommendations from an international collaborative working groupMolecular Genetics and Metabolism 2020; 129(2): 59 doi: 10.1016/j.ymgme.2019.11.004
8
R. Vázquez-Frias, J.E. García-Ortiz, P.F. Valencia-Mayoral, G.E. Castro-Narro, P.G. Medina-Bravo, Y. Santillán-Hernández, J. Flores-Calderón, R. Mehta, C.A. Arellano-Valdés, L. Carbajal-Rodríguez, J.I. Navarrete-Martínez, M.L. Urbán-Reyes, M.T. Valadez-Reyes, F. Zárate-Mondragón, A. Consuelo-Sánchez. Mexican consensus on lysosomal acid lipase deficiency diagnosisRevista de Gastroenterología de México (English Edition) 2018; 83(1): 51 doi: 10.1016/j.rgmxen.2018.01.001
9
Alejandra Consuelo-Sánchez, Rodrigo Vázquez-Frias, Alejandra Reyes-De La Rosa, Carlos P. Acosta-Rodríguez-Bueno, María P. Ortal-Vite, Jorge J. Cebolla. Mutations identified in a cohort of Mexican patients with lysosomal acid lipase deficiencyAnnals of Hepatology 2019; 18(4): 646 doi: 10.1016/j.aohep.2018.07.005
10
Camila da Rosa Witeck, Anne Calbusch Schmitz, Júlia Meller Dias de Oliveira, André Luís Porporatti, Graziela De Luca Canto, Maria Marlene de Souza Pires. Lysosomal acid lipase deficiency in pediatric patients: a scoping reviewJornal de Pediatria 2022; 98(1): 4 doi: 10.1016/j.jped.2021.03.003
11
Katrina J. Besler, Valentin Blanchard, Gordon A. Francis. Lysosomal acid lipase deficiency: A rare inherited dyslipidemia but potential ubiquitous factor in the development of atherosclerosis and fatty liver diseaseFrontiers in Genetics 2022; 13 doi: 10.3389/fgene.2022.1013266
12
Marco Antonio Curiati, Sandra Obikawa Kyosen, Vanessa Gonçalves Pereira, Francy Reis da Silva Patrício, Ana Maria Martins. Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age SpectrumCase Reports in Pediatrics 2018; 2018: 1 doi: 10.1155/2018/4375434
13
Gerarda Cappuccio, Taraka R. Donti, Leroy Hubert, Qin Sun, Sarah H. Elsea. Opening a window on lysosomal acid lipase deficiency: Biochemical, molecular, and epidemiological insightsJournal of Inherited Metabolic Disease 2019; 42(3): 509 doi: 10.1002/jimd.12057
14
O. Sh. Oynotkinova, E. L. Nikonov, A. P. Baranov, E. V. Krukov, M. A. Doroshko. Lysosomal acid lipase deficiency - underestimated cause of dislipidemia. what's new?Dokazatel'naya gastroenterologiya 2018; 7(4): 65 doi: 10.17116/dokgastro2018704165