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Blood antioxidants (vitamin E and β-carotene) in long-term low density lipoprotein apheresis

Clinica chimica acta, 1995-03, Vol.235 (2), p.147-157

1995

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Étude clinique, biologique et génétique de la forme réguliére de la xanthomatose tendineuse hypercholestérol-émique familiale

Atherosclerosis, 1973-09, Vol.18 (2), p.215-233

1973

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2.W13.1 Molecular genetics as tools to redefine the clinics of lipoprotein disorders: The example of lipoprotein lipase deficiency

Atherosclerosis, 1997-10, Vol.134 (1-2), p.110-110

1997

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Plasma factor VII, triglyceride concentration and fibrin degradation products in primary hyperlipidemia: a clinical and laboratory study

Haemostasis, 1989-01, Vol.19 (2), p.83-90

1989

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Recherches sur l'action in vivo du sulfate de protamine sur le sérum humain

Clinica chimica acta, 1959-03, Vol.4 (2), p.231-241

1959

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Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144

Atherosclerosis, 1999-09, Vol.146 (1), p.141-151

1999

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Pseudo-hypertriglycéridémie par déficit en glycérol kinase

La revue de medecine interne, 1989, Vol.10 (5), p.453-456

1989

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Sécrétion isolée de testostérone par une tumeur cortico-surrénale chez une femme ménopausée

La revue de medecine interne, 1986-09, Vol.7 (4), p.371-376

1986

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A description of LDL receptor gene mutations found in France in 105 patients with FH

Atherosclerosis, 2000-07, Vol.151 (1), p.301-301

2000

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1.P.122 Survival and cardiovascular disease in homozygotes and compound heterozygotes for familial hypercholesterolemia treated with LDL-apheresis

Atherosclerosis, 1997-10, Vol.134 (1-2), p.42-42

1997

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Carotid stenosis is a powerful predictor of a positive exercise electrocardiogram in a large hyperlipidemic population

Atherosclerosis, 1992-02, Vol.92 (2), p.105-114

1992

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Evidence of non-deficient low-density lipoprotein receptor patients in a pool of subjects with clinical familial hypercholesterolemia profile

Metabolism, clinical and experimental, 1994-04, Vol.43 (4), p.397-402

1994

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Effect of pravastatin during regressive phase of diet-induced pigeon atherosclerosis

Atherosclerosis, 1994-09, Vol.109 (1), p.314-314

1994

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Effect of pravastatin, a HMG CoA reductase inhibitor, on blood lipids and aortic lipidosis in cholesterol-fed White Carneau pigeons

Biochimica et biophysica acta, 1993-06, Vol.1181 (3), p.279-286

1993

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Investigation of French Canadian founder mutations for lipoprotein lipase deficiency (LPL) in France

Atherosclerosis, 1994-09, Vol.109 (1), p.206-206

1994

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Compound heterozygotes for familial defective apo B-100 (FDB) and familial hypercholesterolemia (FH)

Atherosclerosis, 1994-09, Vol.109 (1), p.206-207

1994

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Founder effect for familial defective apo B-100 (FDB) mutation in France

Atherosclerosis, 1994-09, Vol.109 (1), p.207-207

1994

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An analysis of mutations underlying lipoprotein lipase (LPL) deficiency in France

Atherosclerosis, 1994-09, Vol.109 (1), p.67-68

1994

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Familial defective apo B-100 (FDB) in France: frequency and clinical presentation in families

Atherosclerosis, 1994-09, Vol.109 (1), p.132-132

1994

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Kaposi's sarcoma and HTLV-I infection

The Lancet (British edition), 1990-09, Vol.336 (8714), p.575-575

1990

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Does electrophoresis reliably screen for high serum lipoprotein Lp(a)?

Clinica chimica acta, 1990-04, Vol.188 (1), p.71-77

1990

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Lipoprotein particle analysis comparing simvastatin and fenofibrate

Atherosclerosis, 1991-12, Vol.91, p.S29-S34

1991

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Bartter's syndrome with normal chloride reabsorption during indomethacin treatment

Nephron (2015), 1987, Vol.46 (2), p.137-143

1987

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Ultracentrifugal evidence of a special subtype of mixed hyperlipidemia

Atherosclerosis, 1977-08, Vol.27 (4), p.493-497

1977

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Étude clinique, biologique et génétique de la forme réguliére de la xanthomatose tendineuse hypercholestérol-émique familiale: À propos de 250 observations

Atherosclerosis, 1973, Vol.18 (2), p.215-233

1973

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Blood antioxidants (vitamin E and β-carotene) in long-term low density lipoprotein apheresis

Étude clinique, biologique et génétique de la forme réguliére de la xanthomatose tendineuse hypercholestérol-émique familiale

2.W13.1 Molecular genetics as tools to redefine the clinics of lipoprotein disorders: The example of lipoprotein lipase deficiency

Plasma factor VII, triglyceride concentration and fibrin degradation products in primary hyperlipidemia: a clinical and laboratory study

Recherches sur l'action in vivo du sulfate de protamine sur le sérum humain

Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144

Pseudo-hypertriglycéridémie par déficit en glycérol kinase

Sécrétion isolée de testostérone par une tumeur cortico-surrénale chez une femme ménopausée

A description of LDL receptor gene mutations found in France in 105 patients with FH

1.P.122 Survival and cardiovascular disease in homozygotes and compound heterozygotes for familial hypercholesterolemia treated with LDL-apheresis

Carotid stenosis is a powerful predictor of a positive exercise electrocardiogram in a large hyperlipidemic population

Evidence of non-deficient low-density lipoprotein receptor patients in a pool of subjects with clinical familial hypercholesterolemia profile

Effect of pravastatin during regressive phase of diet-induced pigeon atherosclerosis

Effect of pravastatin, a HMG CoA reductase inhibitor, on blood lipids and aortic lipidosis in cholesterol-fed White Carneau pigeons

Investigation of French Canadian founder mutations for lipoprotein lipase deficiency (LPL) in France

Compound heterozygotes for familial defective apo B-100 (FDB) and familial hypercholesterolemia (FH)

Founder effect for familial defective apo B-100 (FDB) mutation in France

An analysis of mutations underlying lipoprotein lipase (LPL) deficiency in France

Familial defective apo B-100 (FDB) in France: frequency and clinical presentation in families

Kaposi's sarcoma and HTLV-I infection

Does electrophoresis reliably screen for high serum lipoprotein Lp(a)?

Lipoprotein particle analysis comparing simvastatin and fenofibrate

Bartter's syndrome with normal chloride reabsorption during indomethacin treatment

Ultracentrifugal evidence of a special subtype of mixed hyperlipidemia

Étude clinique, biologique et génétique de la forme réguliére de la xanthomatose tendineuse hypercholestérol-émique familiale: À propos de 250 observations

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