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Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency

American journal of human genetics, 1996-08, Vol.59 (2), p.431-436

1996

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Relationship between smoking status and serum lipids in a hyperlipidemic population and analysis of possible confounding factors

Clinical chemistry (Baltimore, Md.), 1992-09, Vol.38 (9), p.1698-1705

1992

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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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Comparison of the efficacy of simvastatin and standard fibrate therapy in the treatment of primary hypercholesterolemia and combined hyperlipidemia

Clinical cardiology (Mahwah, N.J.), 1995-11, Vol.18 (11), p.621-629

1995

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Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

The New England journal of medicine, 1996-09, Vol.335 (12), p.848-854

1996

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An Initiation Codon Mutation in the ApoC-II Gene (ApoC-II Paris) of a Patient with a Deficiency of Apolipoprotein C-II

The Journal of biological chemistry, 1989-12, Vol.264 (35), p.20839-20842

1989

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Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombination

Journal of lipid research, 1995-02, Vol.36 (2), p.356-366

1995

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Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA

Clinical chemistry (Baltimore, Md.), 1994-01, Vol.40 (1), p.24-29

1994

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Hypercholestérolémies chez l'enfant

Journal de pédiatrie et de puériculture, 1996, Vol.9 (1), p.9-16

de Gennes, JL

1996

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Jacques Decourt (1898-1989)

Annales d'endocrinologie, 1990, Vol.51 (3-4), p.99-100

de Gennes, J L

1990

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Increased serum levels of lipoprotein(a) in diabetes mellitus and their reduction with glycemic control

JAMA : the journal of the American Medical Association, 1990-01, Vol.263 (1), p.35-36

1990

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Blood screening of glucose and lipid disorders as coronary atherosclerosis risks factors in French adolescents 16 to 19-20 years old

Annales d'endocrinologie, 2007-10, Vol.68 (5), p.372-383

2007

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The immunocytochemical heterogeneity of silent pituitary adenomas

Acta endocrinologica (Copenhagen), 1988-08, Vol.118 (4), p.533-537

1988

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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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A multicenter comparison of the effects of simvastatin and fenofibrate therapy in severe primary hypercholesterolemia, with particular emphasis on lipoproteins defined by their apolipoprotein composition

Metabolism, clinical and experimental, 1992-05, Vol.41 (5), p.498-503

1992

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Effect of simvastatin on plasma lipids, apolipoproteins and lipoprotein particles in patients with primary hypercholesterolaemia

European journal of clinical pharmacology, 1989-11, Vol.37 (6), p.545-550

1989

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A study of the structural heterogeneity of low-density lipoproteins in two patients homozygous for familial hypercholesterolaemia, one of phenotype E2/2

European journal of clinical investigation, 1986-10, Vol.16 (5), p.329-337

1986

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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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Testicular response to human chorionic gonadotrophin in chronic hyperprolactinaemia

Acta endocrinologica (Copenhagen), 1985-04, Vol.108 (4), p.565-569

1985

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Measurement of two plasma triglyceride lipases by an immunochemical method: studies in patients with hypertriglyceridemia

Journal of lipid research, 1976-05, Vol.17 (3), p.203-210

1976

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Physiopathologie de l'hormone de croissance chez l'homme adulte

Bulletin de l'Académie nationale de médecine, 1984-05, Vol.168 (5-6), p.548-557

DE GENNES, J.-L

1984

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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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Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100

Human mutation, 1996, Vol.7 (4), p.340-345

1996

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Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia

Human mutation, 1998, Vol.11 (S1), p.S141-S144

1998

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Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia

Human genetics, 2002-12, Vol.111 (6), p.501-510

2002

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Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency

Relationship between smoking status and serum lipids in a hyperlipidemic population and analysis of possible confounding factors

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

Comparison of the efficacy of simvastatin and standard fibrate therapy in the treatment of primary hypercholesterolemia and combined hyperlipidemia

Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

An Initiation Codon Mutation in the ApoC-II Gene (ApoC-II Paris) of a Patient with a Deficiency of Apolipoprotein C-II

Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombination

Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA

Hypercholestérolémies chez l'enfant

Jacques Decourt (1898-1989)

Increased serum levels of lipoprotein(a) in diabetes mellitus and their reduction with glycemic control

Blood screening of glucose and lipid disorders as coronary atherosclerosis risks factors in French adolescents 16 to 19-20 years old

The immunocytochemical heterogeneity of silent pituitary adenomas

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

A multicenter comparison of the effects of simvastatin and fenofibrate therapy in severe primary hypercholesterolemia, with particular emphasis on lipoproteins defined by their apolipoprotein composition

Effect of simvastatin on plasma lipids, apolipoproteins and lipoprotein particles in patients with primary hypercholesterolaemia

A study of the structural heterogeneity of low-density lipoproteins in two patients homozygous for familial hypercholesterolaemia, one of phenotype E2/2

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

Testicular response to human chorionic gonadotrophin in chronic hyperprolactinaemia

Measurement of two plasma triglyceride lipases by an immunochemical method: studies in patients with hypertriglyceridemia

Physiopathologie de l'hormone de croissance chez l'homme adulte

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

Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100

Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia

Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia

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