J. de Gennes

发表

[Metastatic pulmonary carcinoma, revealed by Cushing syndrome, initially considered to have a pituitary origin. Course over 25 years].

X. Bertagna, M. Malinsky, D. Kiortsis, 1995, Presse medicale.

Assessment of French patients with LPL deficiency for French Canadian mutations.

M. Hayden, L. Foubert, J. Girardet, 1997, Journal of medical genetics.

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

E. Bruckert, J. Truffert, J. de Gennes, 1992, Clinical chemistry.

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

Y. Grosgogeat, J. Truffert, D. Hermier, 1993, Biochimica et biophysica acta.

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

E. Bruckert, D. Bonnefont-Rousselot, F. Dairou, 1995, Clinica chimica acta; international journal of clinical chemistry.

Interrelationship of plasma triglyceride and coagulant factor VII levels in normotriglyceridemic hypercholesterolemia.

C. Soria, P. Giral, E. Bruckert, 1989, Atherosclerosis.

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

W. Rascher, H. Greten, R. DeGrella, 1976, Journal of lipid research.

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.

J. W. Chisholm, M. Savoldelli, P. Benlian, 1999, Atherosclerosis.

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

M. Hayden, L. Foubert, L. Miao, 1998, Human mutation.

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.

M. Hayden, S. Langlois, L. Foubert, 1996, American journal of human genetics.

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

C. Soria, P. Giral, E. Bruckert, 1989, Haemostasis.

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

G. Luc, J. Fruchart, S. Benhamamouch, 1994, Metabolism: clinical and experimental.

Direct Fetal Blood Examination for Prenatal Diagnosis of Homozygous Familial Hypercholesterolemia

F. Daffos, F. Forestier, F. Dairou, 1985, Arteriosclerosis.

Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method

C. Junien, B. Dastugue, C. Boileau, 1992, Human mutation.

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

P. Giral, E. Bruckert, F. Dairou, 1990, Clinica chimica acta; international journal of clinical chemistry.

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

P. Giral, E. Bruckert, P. Davidoff, 1990, JAMA.

An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-II.

H. Brewer, J. Truffert, C. Parrott, 1989, Journal of Biological Chemistry.

Coagulation factor VII and plasma triglycerides. Decreased catabolism as a possible mechanism of factor VII hyperactivity.

C. Soria, P. Giral, E. Bruckert, 1989, Haemostasis.

Further resolution and comparison of the heterogeneity of plasma low-density lipoproteins in human hyperlipoproteinemias: type III hyperlipoproteinemia, hypertriglyceridemia and familial hypercholesterolemia.

G. Luc, M. Chapman, J. de Gennes, 1988, Atherosclerosis.

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

E. Bruckert, W. Malbecq, F. Baigts, 1995, Clinical cardiology.

[A case of 46 XX gonadoblastoma].

J. de Grouchy, C. Pélissier, H. Yaneva, 1970, Annales d'endocrinologie.

[Results of bromocriptine treatment of giant or invasive prolactin adenomas. Apropos of 20 cases].

H. Scherrer, H. Heshmati, G. Turpin, 1985, Annales de medecine interne.

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

M. Krempf, P. Moulin, J. Girardet, 2002, Human Genetics.

[How to explore and interpret a case of hyperlipemia].

J. Hamburger, J. de Gennes, H. Péquignot, 1966, La Presse medicale.

[Preliminary study of antidiuretic effect of clofibrate (or atromid S) in pitressosensitive diabetes insipidus].

J. Truffert, J. de Gennes, B. Bigorie, 1970, Annales d'endocrinologie.

[Analgesic effect on headaches of octreotide, a somatostatin analogue, in a case of non-functioning pituitary adenoma].

L. Foubert, M. Kujas, G. Turpin, 1991, Presse medicale.

[Hyperlipemias due to alcohol].

J. Truffert, J. de Gennes, P. Thomopoulos, 1972, Nutrition and metabolism.

Antidiuretic effect of clofibrate in therapy of diabetes insipidus.

J. Truffert, J. de Gennes, B. Bigorie, 1973, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

The immunocytochemical heterogeneity of silent pituitary adenomas.

H. Heshmati, R. van Effenterre, M. Kujas, 1988, Acta endocrinologica.

[The heart in Turner-Ullrich syndrome. (Study of 26 personal cases and review of cases comprising a chromosomal study)].

I. Emerit, P. Vernant, J. de Grouchy, 1966, Archives des maladies du coeur et des vaisseaux.

Lipoprotein Lp(a) in homozygous familial hypercholesterolemia: density profile, particle heterogeneity and apolipoprotein(a) phenotype.

E. Bruckert, M. J. Chapman, J. Farriaux, 1991, Atherosclerosis.

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

G. Béréziat, J. D. de Gennes, P. Richard, 1994, Clinical chemistry.

Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene.

M. Hayden, L. Foubert, P. Benlian, 1996, The New England journal of medicine.

Panhypopituitarism secondary to head trauma: evidence for a hypothalamic origin of the deficit.

S. Jambart, G. Turpin, J. de Gennes, 1980, Acta endocrinologica.

[Homozygous cutaneo-tendinous forms of hypercholesteremic xanthomatosis in an exemplary familial case. Trial of plasmapheresis ans heroic treatment].

R. Touraine, J. Truffert, J. de Gennes, 1967, Bulletins et memoires de la Societe medicale des hopitaux de Paris.

Double screening test at 8th and 12th hour of overnight fasting for a better classification of idiopathic hyperlipidemias. Large scale study of 505 tests.

F. Dairou, J. Truffert, J. de Gennes, 1981, Diabete & metabolisme.

Identification of a new apolipoprotein E variant (E2 Arg142-->Leu) in type III hyperlipidemia.

I. Beucler, J. D. de Gennes, P. Richard, 1995, Atherosclerosis.

[Combined oral contraceptives].

E. Baulieu, J. Ferin, H. Rozenbaum, 1973, Fertilite, orthogenie.

Bartter's syndrome with normal chloride reabsorption during indomethacin treatment.

M. Kazatchkine, J. Bariéty, J. Truffert, 1987, Nephron.

Molecular genetics of apoC-II and lipoprotein lipase deficiency.

H. Brewer, A. Stalenhoef, J. Brunzell, 1991, Advances in experimental medicine and biology.

Testicular response to human chorionic gonadotrophin in chronic hyperprolactinaemia.

A. Carayon, H. Heshmati, A. Gueguen, 1985, Acta endocrinologica.

Pituitary prolactinoma, adrenal aldosterone-producing adenomas, gastric schwannoma and colonic polyadenomas: a possible variant of multiple endocrine neoplasia (MEN) type I.

J. Cabane, J. de Gennes, R. Doumith, 1982, Acta endocrinologica.

[Review of the metabolic and endocrine examination of a case of lipoatrophic diabetes].

M. Appelbaum, J. Trémoliéres, J. de Gennes, 1967, La Presse medicale.

[Detection and distriburion of slow pre-betalipoprotein in agar gel electrophoresis of total serum in 204 cases of mixed hyperlipidemia].

J. Truffert, J. de Gennes, J. F. Colas-Belcourt, 1975, Annales de medecine interne.

[A rare cause of amenorrhea: stenosis of the aqueduct of Sylvius. Apropos of 3 cases. Cure by ventriculo-atrial shunt].

H. Heshmati, G. Turpin, J. de Gennes, 1983, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

[Metabolism of free fatty acids].

J. Hanoune, J. de Gennes, H. Saltiel, 1965, La Revue du praticien.

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries

M. Hayden, J. Kastelein, D. Chitayat, 1994, Human mutation.

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

L. Foubert, J. Hamelin, D. Brault, 1995, Journal of lipid research.

Lp(a) levels in different types of dyslipidemia in the French population.

G. Chatellier, E. Bruckert, F. Dairou, 1990, Atherosclerosis.

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

G. Béréziat, E. Villain, P. Benlian, 1996, Human mutation.

Results of the study of apolipoprotein E and its isomorphs on isoelectric focusing in dyslipoproteinemias.

G. Luc, E. Bruckert, F. Dairou, 1987, Advances in experimental medicine and biology.

[Residual ovarian function after minidoses of estroprogestative agents].

J. Colau, R. Taurelle, J. de Gennes, 1983, Journal de gynecologie, obstetrique et biologie de la reproduction.

Absence of inhibition by lipoprotein (a) inhibition of tPA induced thrombolysis in a patient's plasma milieu.

J. Soria, C. Soria, A. Legrand, 1990, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

[Thrombosis of the right internal carotid artery following continuous contraceptive treatment with chlormadinone acetate in a 28-year-old woman].

J. Truffert, G. Turpin, J. de Gennes, 1971, La Presse medicale.

[Detection of a terrain of familial hyperlipemia in 2 women who, before the age of 30 years, were victims of a cerebral vascular accident while under treatment with hormonal contraceptives].

F. Thervet, J. de Gennes, 1967, Bulletin de l'Academie nationale de medecine.