Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1865-8652
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia ; volume:36 ; number:7 ; day:17 ; month:5 ; year:2019 ; pages:1786-1811 ; date:7.2019
Advances in therapy ; 36, Heft 7 (17.5.2019), 1786-1811, 7.2019
- Creator
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Ben-Omran, Tawfeg
Masana, Luis
Kolovou, Genovefa
Ariceta, Gema
Nóvoa, F. Javier
Lund, Allan M.
Bogsrud, Martin P.
Araujo, María
Hussein, Osamah
Ibarretxe, Daiana
Sanchez-Hernández, Rosa M.
Santos, Raul D.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s12325-019-00985-8
- URN
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urn:nbn:de:101:1-2019103100100289359392
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:26 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ben-Omran, Tawfeg
- Masana, Luis
- Kolovou, Genovefa
- Ariceta, Gema
- Nóvoa, F. Javier
- Lund, Allan M.
- Bogsrud, Martin P.
- Araujo, María
- Hussein, Osamah
- Ibarretxe, Daiana
- Sanchez-Hernández, Rosa M.
- Santos, Raul D.
- SpringerLink (Online service)
Other Objects (12)
Correction to: Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia
Target achievement and cardiovascular event rates with Lomitapide in homozygous Familial Hypercholesterolaemia
A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke
Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis
A machine-learning algorithm using claims data to identify patients with homozygous familial hypercholesterolemia
Vascular access for lipid apheresis: a challenge in young children with homozygous familial hypercholesterolemia
Short-term evolocumab-induced tendon xanthomas regression in an elderly patient with homozygous familial hypercholesterolemia
Homozygous Familial Hypercholesterolemia (HoFH) in Saudi Arabia and Two Cases of Lomitapide Use in a Real-World Setting
A Case Series Assessing the Effects of Lomitapide on Carotid Intima-Media Thickness in Adult Patients with Homozygous Familial Hypercholesterolaemia in a Real-World Setting
Long-term effectiveness and safety of lomitapide in patients with homozygous familial hypercholesterolemia: an observational case series
A homozygous R148W mutation in Semaphorin 7A causes progressive familial intrahepatic cholestasis
Metabolic systems approaches update molecular insights of clinical phenotypes and cardiovascular risk in patients with homozygous familial hypercholesterolemia
Correction to: Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia
Target achievement and cardiovascular event rates with Lomitapide in homozygous Familial Hypercholesterolaemia
A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke
Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis
A machine-learning algorithm using claims data to identify patients with homozygous familial hypercholesterolemia
Vascular access for lipid apheresis: a challenge in young children with homozygous familial hypercholesterolemia
Short-term evolocumab-induced tendon xanthomas regression in an elderly patient with homozygous familial hypercholesterolemia
Homozygous Familial Hypercholesterolemia (HoFH) in Saudi Arabia and Two Cases of Lomitapide Use in a Real-World Setting
A Case Series Assessing the Effects of Lomitapide on Carotid Intima-Media Thickness in Adult Patients with Homozygous Familial Hypercholesterolaemia in a Real-World Setting
Long-term effectiveness and safety of lomitapide in patients with homozygous familial hypercholesterolemia: an observational case series
A homozygous R148W mutation in Semaphorin 7A causes progressive familial intrahepatic cholestasis
Metabolic systems approaches update molecular insights of clinical phenotypes and cardiovascular risk in patients with homozygous familial hypercholesterolemia
Correction to: Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia
Target achievement and cardiovascular event rates with Lomitapide in homozygous Familial Hypercholesterolaemia
A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke
Pregnancy in a Woman with Homozygous Familial Hypercholesterolemia Not on Low-Density Lipoprotein Apheresis
A machine-learning algorithm using claims data to identify patients with homozygous familial hypercholesterolemia
Vascular access for lipid apheresis: a challenge in young children with homozygous familial hypercholesterolemia
Short-term evolocumab-induced tendon xanthomas regression in an elderly patient with homozygous familial hypercholesterolemia
Homozygous Familial Hypercholesterolemia (HoFH) in Saudi Arabia and Two Cases of Lomitapide Use in a Real-World Setting
A Case Series Assessing the Effects of Lomitapide on Carotid Intima-Media Thickness in Adult Patients with Homozygous Familial Hypercholesterolaemia in a Real-World Setting
Long-term effectiveness and safety of lomitapide in patients with homozygous familial hypercholesterolemia: an observational case series
A homozygous R148W mutation in Semaphorin 7A causes progressive familial intrahepatic cholestasis