152 related articles for article (PubMed ID: 31113597)
1. Lysosomal Acid Lipase Deficiency Leading to Liver Cirrhosis: a Case Report of a Rare Variant Mutation.
Cunha-Silva M; Mazo DFC; Corrêa BR; Lopes TM; Arrelaro RC; Ferreira GL; Rabello MI; Sevá-Pereira T; Escanhoela CAF; Almeida JRS
Ann Hepatol; 2019; 18(1):230-235. PubMed ID: 31113597
[TBL] [Abstract][Full Text] [Related]
2. Lysosomal Acid Lipase Deficiency, a Rare Pathology: The First Pediatric Patient Reported in Colombia.
Botero V; Garcia VH; Gomez-Duarte C; Aristizabal AM; Arrunategui AM; Echeverri GJ; Pachajoa H
Am J Case Rep; 2018 Jun; 19():669-672. PubMed ID: 29884776
[TBL] [Abstract][Full Text] [Related]
3. Identification of rare diseases by screening a population selected on the basis of routine pathology results-the PATHFINDER project: lysosomal acid lipase/cholesteryl ester storage disease substudy.
Reynolds TM; Mewies C; Hamilton J; Wierzbicki AS;
J Clin Pathol; 2018 Jul; 71(7):608-613. PubMed ID: 29358478
[TBL] [Abstract][Full Text] [Related]
4. The global prevalence and genetic spectrum of lysosomal acid lipase deficiency: A rare condition that mimics NAFLD.
Carter A; Brackley SM; Gao J; Mann JP
J Hepatol; 2019 Jan; 70(1):142-150. PubMed ID: 30315827
[TBL] [Abstract][Full Text] [Related]
5. Hepatic cholesteryl ester accumulation in lysosomal acid lipase deficiency: non-invasive identification and treatment monitoring by magnetic resonance.
Thelwall PE; Smith FE; Leavitt MC; Canty D; Hu W; Hollingsworth KG; Thoma C; Trenell MI; Taylor R; Rutkowski JV; Blamire AM; Quinn AG
J Hepatol; 2013 Sep; 59(3):543-9. PubMed ID: 23624251
[TBL] [Abstract][Full Text] [Related]
6. Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency.
Santillán-Hernández Y; Almanza-Miranda E; Xin WW; Goss K; Vera-Loaiza A; Gorráez-de la Mora MT; Piña-Aguilar RE
World J Gastroenterol; 2015 Jan; 21(3):1001-8. PubMed ID: 25624737
[TBL] [Abstract][Full Text] [Related]
7. Childhood/adult-onset lysosomal acid lipase deficiency: A serious metabolic and vascular phenotype beyond liver disease-four new pediatric cases.
Poinsot P; Collardeau Frachon S; Restier L; Sérusclat A; Di Filippo M; Charrière S; Moulin P; Lachaux A; Peretti N
J Clin Lipidol; 2017; 11(1):167-177.e3. PubMed ID: 28391883
[TBL] [Abstract][Full Text] [Related]
8. Sebelipase alfa in children and adults with lysosomal acid lipase deficiency: Final results of the ARISE study.
Burton BK; Feillet F; Furuya KN; Marulkar S; Balwani M
J Hepatol; 2022 Mar; 76(3):577-587. PubMed ID: 34774639
[TBL] [Abstract][Full Text] [Related]
9. Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants.
Pisciotta L; Tozzi G; Travaglini L; Taurisano R; Lucchi T; Indolfi G; Papadia F; Di Rocco M; D'Antiga L; Crock P; Vora K; Nightingale S; Michelakakis H; Garoufi A; Lykopoulou L; Bertolini S; Calandra S
Atherosclerosis; 2017 Oct; 265():124-132. PubMed ID: 28881270
[TBL] [Abstract][Full Text] [Related]
10. Pediatric patients with lysosomal acid lipase deficiency.
Suarez-Zamora DA; Rojas-Rojas MM; Ordoñez-Guerrero F; Mugnier-Quijano J; Lopez-Panqueva R
Rev Esp Patol; 2023; 56(2):113-118. PubMed ID: 37061237
[TBL] [Abstract][Full Text] [Related]
11. A Case of Lysosomal Acid Lipase Deficiency Confirmed by Response to Sebelipase Alfa Therapy.
Shen JJ; Davis JL; Hong X; Laningham FH; Gelb MH; Kim GE
J Pediatr Gastroenterol Nutr; 2020 Dec; 71(6):726-730. PubMed ID: 32740531
[TBL] [Abstract][Full Text] [Related]
12. Managing Cardiovascular Risk in Lysosomal Acid Lipase Deficiency.
Maciejko JJ
Am J Cardiovasc Drugs; 2017 Jun; 17(3):217-231. PubMed ID: 28197978
[TBL] [Abstract][Full Text] [Related]
13. [Wolman disease with novel mutation of LIPA gene in a Chinese infant].
Huang YL; Sheng HY; Zhao XY; Yu JK; Li L; Liu HS; Gu CM; He DM; Liu L
Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):601-5. PubMed ID: 23158738
[TBL] [Abstract][Full Text] [Related]
14. Intragenic deletion as a novel type of mutation in Wolman disease.
Lee TM; Welsh M; Benhamed S; Chung WK
Mol Genet Metab; 2011 Dec; 104(4):703-5. PubMed ID: 21963785
[TBL] [Abstract][Full Text] [Related]
15. Cholesteryl ester storage disease: a rare and possibly treatable cause of premature vascular disease and cirrhosis.
Reynolds T
J Clin Pathol; 2013 Nov; 66(11):918-23. PubMed ID: 23999269
[TBL] [Abstract][Full Text] [Related]
16. Reduced lysosomal acid lipase activity: A new marker of liver disease severity across the clinical continuum of non-alcoholic fatty liver disease?
Baratta F; Pastori D; Ferro D; Carluccio G; Tozzi G; Angelico F; Violi F; Del Ben M
World J Gastroenterol; 2019 Aug; 25(30):4172-4180. PubMed ID: 31435171
[TBL] [Abstract][Full Text] [Related]
17. Differential Diagnosis of a Patient with Lysosomal Acid Lipase Deficiency: A Case Report.
Akki AS; Chung SM; Rudolph BJ; Ewart MR
Lab Med; 2018 Oct; 49(4):377-384. PubMed ID: 29982809
[TBL] [Abstract][Full Text] [Related]
18. 15-Year progression to liver cancer in the lack of treatment for lysosomal acid lipase deficiency: A case report.
Cunha-Silva M; de França EVC; Veiga CT; Greca RD; de Moraes PBS; de Campos Mazo DF; de Ataíde EC; Perales SR; Monici LT; Sevá-Pereira T
Medicine (Baltimore); 2022 Sep; 101(35):e30315. PubMed ID: 36107601
[TBL] [Abstract][Full Text] [Related]
19. A Rare Image of Liver Steatosis - Acid Lipase Lysosomal Deficiency.
Calian I; Rusu I; Sabo CM; Ciobanu L
J Gastrointestin Liver Dis; 2020 Mar; 29(1):5. PubMed ID: 32176755
[No Abstract] [Full Text] [Related]
20. A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant.
Anushiravani A; Jafari Khamirani H; Mohamadkhani A; Mani A; Dianatpour M; Malekzadeh R
Arch Iran Med; 2023 Feb; 26(2):86-91. PubMed ID: 37543928
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
