Search Results - "Beliard, S."

Improvement in LDL-cholesterol levels of patients with familial hypercholesterolemia: Can we do better? Analysis of results obtained during the past two decades in 1669 French subjects by Béliard, S, Carreau, V, Carrié, A, Giral, P, Duchêne, E, Farnier, M, Ferrières, J, Fredenrich, A, Krempf, M, Luc, G, Moulin, P, Bruckert, E

“…Abstract Background Heterozygous Familial Hypercholesterolemia (heFH) is an autosomal disease that affects about 1/500 people. It is characterized by markedly…”
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Metabolic syndrome in adults who received hematopoietic stem cell transplantation for acute childhood leukemia: an LEA study by Oudin, C, Auquier, P, Bertrand, Y, Contet, A, Kanold, J, Sirvent, N, Thouvenin, S, Tabone, M-D, Lutz, P, Ducassou, S, Plantaz, D, Dalle, J-H, Gandemer, V, Beliard, S, Berbis, J, Vercasson, C, Barlogis, V, Baruchel, A, Leverger, G, Michel, G

“…We evaluated prospectively the incidence and risk factors of the metabolic syndrome (MS) and its components in 170 adult patients (mean age at evaluation:…”
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Changes in femoral artery blood flow during thermoneutral, cold, and contrast-water therapy by Ménétrier, A, Béliard, S, Ravier, G, Mourot, L, Bouhaddi, M, Regnard, J, Tordi, N

“…The purpose of this study was to examine the changes in femoral artery blood flow during cold water immersion (CWI), contrast water therapy (CWT) and…”
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Consensus statement on the management of dyslipidaemias in adults by Béliard, S, Bonnet, F, Bouhanick, B, Bruckert, E, Cariou, B, Charrière, S, Durlach, V, Moulin, P, Valéro, R, Vergès, B

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Parallel increase of plasma apoproteins C-II and C-III in Type 2 diabetic patients by Béliard, S., Nogueira, J. P., Maraninchi, M., Lairon, D., Nicolay, A., Giral, P., Portugal, H., Vialettes, B., Valéro, R.

“…Aims  To determine plasma levels of apoprotein (apo) C‐II and apoprotein C‐III in Type 2 diabetic patients and to examine the clinical and biological factors…”
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Consensus statement on the management of dyslipidaemias in adults by Béliard, S, Bonnet, F, Bouhanick, B, Bruckert, E, Cariou, B, Charrière, S, Durlach, V, Moulin, P, Valéro, R, Vergès, B

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Scleredema adultorum of Buschke: an under recognized skin complication of diabetes by Meguerditchian, C, Jacquet, P, Béliard, S, Benderitter, T, Valéro, R, Carsuzza, F, Vialettes, B

“…Scleredema of Buschke or scleredema diabetorum is a skin complication of diabetes with deposits of collagen and aminoglycans in the dermis. This disease…”
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Statin and cardiovascular diseases after 75 years by Retornaz, F, Beliard, S, Gremeaux, E, Chiche, L, Lagarde, L, Andrianasolo, M, Molines, C, Oliver, C

“…Statin prescription in persons older than 75 years or with frailty signs raises questions on the role of cholesterol in the genesis of atherosclerosis in this…”
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The effects of a calf pump device on second half performance of a simulated soccer match in competitive youth players by Béliard, S., Cassirame, J., Ennequin, G., Coratella, G., Tordi, N.

“…During soccer matches, performance decrements have been reported that relate to both physical abilities and technical skills. To investigate the effects of…”
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Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) by Mosbah, H, Donadille, B, Vatier, C, Janmaat, S, Atlan, M, Badens, C, Barat, P, Béliard, S, Beltrand, J, Ben Yaou, R, Bismuth, E, Boccara, F, Cariou, B, Chaouat, M, Charriot, G, Christin-Maitre, S, De Kerdanet, M, Delemer, B, Disse, E, Dubois, N, Eymard, B, Fève, B, Lascols, O, Mathurin, P, Nobécourt, E, Poujol-Robert, A, Prevost, G, Richard, P, Sellam, J, Tauveron, I, Treboz, D, Vergès, B, Vermot-Desroches, V, Wahbi, K, Jéru, I, Vantyghem, M C, Vigouroux, C

“…Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA…”
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High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia Registry by Béliard, Sophie, Boccara, Franck, Cariou, Bertrand, Carrié, Alain, Collet, Xavier, Farnier, Michel, Ferrières, Jean, Krempf, Michael, Peretti, Noël, Rabès, Jean-Pierre, Varret, Mathilde, Vimont, Alexandre, Charrière, Sybil, Bruckert, Eric, Angoulvant, D., Béliard, S., Benlian, P., Boileau, C., Boccara, F., Bruckert, E., Cariou, B., Carreau, V., Carrié, A., Charrière, S., Di Filippo, M., Ducluzeau, P.H., Dulong, S., Durlach, V., Farnier, M., Ferrari, E., Ferrières, J., Gallo, A., Girardet, J.P., Hankard, R., Krempf, M., Lalau, J.D., Lefort, B., Lemale, J., Moulin, P., Paillard, F., Peretti, N., Pradignac, A., Pucheu, Y., Rabès, J.P., Saheb, S., Sultan, A., Tounian, P., Valéro, R., Varret, M., Vergès, B., Yelnik, C., Ziegler, O.

“…Cardiovascular risk is high in heterozygous familial hypercholesterolemia (HeFH). The objective of this study was to describe recurrent cardiovascular events…”
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Maternal inheritance of a genetic mutation for familial hypercholesterolemia predispose to coronary atherosclerosis in adulthood by Mourre, F., Giorgi, R., Beliard, S., Valero, R.

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Dutch score relevance for assessing the probability of familial hypercholesterolemia diagnosis by Cattieuw, L., Mourre, F., Chtioui, H., Bégu-Le Corroller, A., Dubois, N., Grangeot, R., Carrié, A., Beliard, S., Valero, R.

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Molecular spectrum of PCSK9-based FH in FRANCE, The French P.(SER127ARG) founder variant by Azar, Y., Abou-Khalil, Y., Di-Filippo, M., Carrie, A., Beliard, S., Boileau, C., Fadel, M. Abi, Rabes, J.-P., Varret, M.

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Efficient rituximab therapy in a patient with an autoimmune type i hyperlipidemia by Béliard, S, Ete, M, Poullin, P, Maraninchi, M, Di Filippo, M, Moulin, P, Kaplanski, G, Valéro, R

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Growth hormone (GH) and triglyceride-rich lipoprotein (TRL) metabolism: Effect of one month of discontinued growth hormone treatment in growth hormone deficient patients by Calabrese, A., Nicolay, A., Wolff, E., Dupont, J., Valero, R., Beliard, S., Maraninchi, M.

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Familial hypercholesterolemia: A largely underestimated cardiovascular risk by Ferrières, J, Bruckert, É, Béliard, S, Rabès, J-P, Farnier, M, Krempf, M, Cariou, B, Danchin, N

“…Familial hypercholesterolemia is a monogenic autosomal dominant dyslipidemia characterized by a permanent and isolated increase of cholesterol carried by…”
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Evaluation of new polygenic risk scores in the diagnosis of familial hypercholesterolemia by Vanhoye, X., Bardel, C., Rimbert, A., Moulin, P., Rollat-Farnier, P.-A., Muntaner, M., Marmontel, O., Peretti, N., Fournier, C., Pichelin, M., Beliard, S., Charrière, S., Dumont, S., Dira, R., Cariou, B., Meirhaeghe, A., Di Filippo, M.

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Cardiovascular Events According To Maternal Or Paternal Heritability Of Genetic Mutation In Familial Hypercholesterolemia by Mourre, F., Beliard, S., Valero, R., Giorgi, R.

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Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis by Peretti, Noel, Vimont, Alexandre, Mas, Emmanuel, Ferrières, Jean, Tounian, Patrick, Lemale, Julie, Boccara, Franck, Di Filippo, Mathilde, Charriere, Sybil, Moulin, Philippe, Poinsot, Pierre, Cottin, Yves, Ducluzeau, Pierre-Henri, Dourmap, Caroline, Cariou, Bertrand, Farnier, Michel, Paillard, François, Pradignac, Alain, Yelnik, Cécile, Gallo, Antonio, Bruckert, Eric, Beliard, Sophie

“…To identify childhood and parental factors associated with initiation of statin therapy in children with heterozygous familial hypercholesterolemia (HeFH),…”
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