Fatty Liver and Systemic Atherosclerosis in a Young, Lean Patient: Rule Out Lysosomal Acid Lipase Deficiency

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Fatty Liver and Systemic Atherosclerosis in a Young, Lean Patient: Rule Out Lysosomal Acid Lipase Deficiency ; volume:13 ; number:3 ; year:2019 ; pages:498-507
Case reports in gastroenterology ; 13, Heft 3 (2019), 498-507

Creator: Zharkova, Maria
Nekrasova, Tatiana
Ivashkin, Vladimir
Maevskaya, Marina
Strokova, Tatyana

DOI: 10.1159/000504646

URN: urn:nbn:de:101:1-2020100101334075904440

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:55 AM CEST

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Zharkova, Maria
Nekrasova, Tatiana
Ivashkin, Vladimir
Maevskaya, Marina
Strokova, Tatyana

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“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

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Adipose triglyceride lipase in immune response, inflammation, and atherosclerosis

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“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

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Lysosomal acid lipase regulates VLDL synthesis and insulin sensitivity in mice

Adipose triglyceride lipase in immune response, inflammation, and atherosclerosis

Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification

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Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis

“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia

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Fatty Liver and Systemic Atherosclerosis in a Young, Lean Patient: Rule Out Lysosomal Acid Lipase Deficiency

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Other Objects (12)

Hepatosteatosis from Lysosomal Acid Lipase Deficiency

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency

Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy

Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study

Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology

Lysosomal acid lipase regulates VLDL synthesis and insulin sensitivity in mice

Adipose triglyceride lipase in immune response, inflammation, and atherosclerosis

Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis

“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia

Hepatosteatosis from Lysosomal Acid Lipase Deficiency

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency

Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy

Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study

Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology

Lysosomal acid lipase regulates VLDL synthesis and insulin sensitivity in mice

Adipose triglyceride lipase in immune response, inflammation, and atherosclerosis

Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis

“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia

Hepatosteatosis from Lysosomal Acid Lipase Deficiency

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency

Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy

Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study

Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology

Lysosomal acid lipase regulates VLDL synthesis and insulin sensitivity in mice

Adipose triglyceride lipase in immune response, inflammation, and atherosclerosis

Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

Sex hormones affect endothelial lipase-mediated lipid metabolism and atherosclerosis

“Why them, why me, why us?” The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study

Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia

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