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Beyond LDL-C lowering: distinct molecular sphingolipids are good indicators of proprotein convertase subtilisin/kexin type 9 (PCSK9) deficiency. [electronic resource] by
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- Tarasov, Kirill
- Ta, Hung Xuan
- Suoniemi, Matti
- Ekroos, Kim
- Hurme, Reini
- Lehtimäki, Terho
- Päivä, Hannu
- Kleber, Marcus E
- März, Winfried
- Prat, Annik
- Seidah, Nabil G
- Laaksonen, Reijo
Producer: 20131021
In:
Atherosclerosis vol. 228
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Impact of protease inhibitors on circulating PCSK9 levels in HIV-infected antiretroviral-naive patients from an ongoing prospective cohort. [electronic resource] by
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- Ghislain, Mathilde
- Meyer, Laurence
- Goujard, Cecile
- Le May, Cedric
- Vigouroux, Corinne
- Bastard, Jean P
- Fellahi, Soraya
- Capeau, Jacqueline
- Cohen, Ariel
- Cariou, Bertrand
Producer: 20180604
In:
AIDS (London, England) vol. 31
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A PCSK9 variant and familial combined hyperlipidaemia. [electronic resource] by
- Abifadel, M
- Bernier, L
- Dubuc, G
- Nuel, G
- Rabès, J-P
- Bonneau, J
- Marques, A
- Marduel, M
- Devillers, M
- Munnich, A
- Erlich, D
- Varret, M
- Roy, M
- Davignon, J
- Boileau, C
Producer: 20090202
In:
Journal of medical genetics vol. 45
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Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease). [electronic resource] by
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- Bonneau, Jessica
- Bonnefont-Rousselot, Dominique
- Champigneulle, Jacqueline
- Rabès, Jean P
- Abifadel, Marianne
- Aparicio, Thomas
- Guenedet, Jean C
- Bruckert, Eric
- Boileau, Catherine
- Morali, Alain
- Varret, Mathilde
- Aggerbeck, Lawrence P
- Samson-Bouma, Marie E
Producer: 20110509
In:
Orphanet journal of rare diseases vol. 6
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650.
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The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene. [electronic resource] by
- Abifadel, Marianne
- Rabès, Jean-Pierre
- Jambart, Sélim
- Halaby, Georges
- Gannagé-Yared, Marie-Hélène
- Sarkis, Antoine
- Beaino, Ghada
- Varret, Mathilde
- Salem, Nabiha
- Corbani, Sandra
- Aydénian, Hermine
- Junien, Claudine
- Munnich, Arnold
- Boileau, Catherine
Producer: 20090923
In:
Human mutation vol. 30
Availability: No items available.
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