These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 8432549)

  • 41. 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]  

  • 42. Opening a window on lysosomal acid lipase deficiency: Biochemical, molecular, and epidemiological insights.
    Cappuccio G; Donti TR; Hubert L; Sun Q; Elsea SH
    J Inherit Metab Dis; 2019 May; 42(3):509-518. PubMed ID: 30684275
    [TBL] [Abstract][Full Text] [Related]  

  • 43. New diagnostic method for lysosomal acid lipase deficiency and the need to recognize its manifestation in infants (Wolman disease).
    Gómez-Nájera M; Barajas-Medina H; Gallegos-Rivas MC; Mendez-Sashida P; Goss KA; Sims KB; Tripuraneni R; Valles-Ayoub Y
    J Pediatr Gastroenterol Nutr; 2015 Mar; 60(3):e22-4. PubMed ID: 24048164
    [No Abstract]   [Full Text] [Related]  

  • 44. [Wolman disease: report of a case].
    Ma YY; Chen L
    Zhonghua Bing Li Xue Za Zhi; 2013 Apr; 42(4):276-7. PubMed ID: 23928541
    [No Abstract]   [Full Text] [Related]  

  • 45. Lysosomal acid lipase A and the hypercholesterolaemic phenotype.
    Fouchier SW; Defesche JC
    Curr Opin Lipidol; 2013 Aug; 24(4):332-8. PubMed ID: 23652569
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Lysosomal acid lipase mutations that determine phenotype in Wolman and cholesterol ester storage disease.
    Anderson RA; Bryson GM; Parks JS
    Mol Genet Metab; 1999 Nov; 68(3):333-45. PubMed ID: 10562460
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Large-scale functional LIPA variant characterization to improve birth prevalence estimates of lysosomal acid lipase deficiency.
    Del Angel G; Hutchinson AT; Jain NK; Forbes CD; Reynders J
    Hum Mutat; 2019 Nov; 40(11):2007-2020. PubMed ID: 31180157
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis.
    Tinsa F; Ben Romdhane M; Boudabous H; Bel Hadj I; Brini I; Tebib N; Louati H; Bekri S; Boussetta K
    J Pediatr Hematol Oncol; 2019 Apr; 41(3):e193-e196. PubMed ID: 29702543
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Altered mononuclear phagocyte differentiation associated with genetic defects of the lysosomal acid lipase.
    Rothe G; Stöhr J; Fehringer P; Gasche C; Schmitz G
    Atherosclerosis; 1997 Apr; 130(1-2):215-21. PubMed ID: 9126667
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Structure-based virtual screening to identify potential lipase inhibitors to reduce lipid storage in Wolman disorder.
    Vasudevan K; Udhaya Kumar S; Mithun A; Raghavendra B; George Priya Doss C
    Adv Protein Chem Struct Biol; 2023; 133():351-363. PubMed ID: 36707205
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Wolman's disease in an infant].
    Storm W; Wendel U; Sprenkamp M; Seidler A
    Monatsschr Kinderheilkd; 1990 Feb; 138(2):88-90. PubMed ID: 2320017
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Overexpression of lysosomal acid lipase and other proteins in atherosclerosis.
    Zschenker O; Illies T; Ameis D
    J Biochem; 2006 Jul; 140(1):23-38. PubMed ID: 16877765
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease.
    Chabchoub I; Boudabbous H; Maaloul I; Ben Abdelaziz R; Ben Chehida A; Ayadi L; Kamoun T; Tebib N; Boudaouara T; Bekri S; Hachicha M
    J Pediatr Hematol Oncol; 2020 May; 42(4):310-312. PubMed ID: 31318819
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Options to consider when treating lysosomal acid lipase deficiency.
    Block RC; Razani B
    J Clin Lipidol; 2016; 10(5):1280-1. PubMed ID: 27678449
    [No Abstract]   [Full Text] [Related]  

  • 57. 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]  

  • 58. Does Lysosomial Acid Lipase Reduction Play a Role in Adult Non-Alcoholic Fatty Liver Disease?
    Baratta F; Pastori D; Polimeni L; Tozzi G; Violi F; Angelico F; Del Ben M
    Int J Mol Sci; 2015 Nov; 16(12):28014-21. PubMed ID: 26602919
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Acid lipase deficiency (Wolman disease and cholesteryl ester storage disease: CESD)].
    Tanaka A
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):427-30. PubMed ID: 9645100
    [No Abstract]   [Full Text] [Related]  

  • 60. Assignment of the GDH loci to human chromosomes 10q23 and Xq24 by in situ hybridization.
    Jung KY; Warter S; Rumpler Y
    Ann Genet; 1989; 32(2):109-10. PubMed ID: 2757358
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.