Lagarde JP - Search Results

1

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

Foubert L, De Gennes JL, Lagarde JP, Ehrenborg E, Raisonnier A, Girardet JP, Hayden MR, Benlian P. Foubert L, et al. Among authors: lagarde jp. J Med Genet. 1997 Aug;34(8):672-5. doi: 10.1136/jmg.34.8.672. J Med Genet. 1997. PMID: 9279761 Free PMC article.

2

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

Benlian P, de Gennes JL, Dairou F, Hermelin B, Ginon I, Villain E, Lagarde JP, Federspiel MC, Bertrand V, Bernard C, Bereziat G. Benlian P, et al. Among authors: lagarde jp. Hum Mutat. 1996;7(4):340-5. doi: 10.1002/(SICI)1098-1004(1996)7:4<340::AID-HUMU8>3.0.CO;2-C. Hum Mutat. 1996. PMID: 8723684

3

[Genotyping of apolipoprotein E (alleles epsilon 2, epsilon 3 and epsilon 4) from capillary blood].

Lagarde JP, Benlian P, Zekraoui L, Raisonnier A. Lagarde JP, et al. Ann Biol Clin (Paris). 1995;53(1-2):15-20. Ann Biol Clin (Paris). 1995. PMID: 7574085 French.

4

Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele.

Abdel-Wareth LO, Pimstone SN, Lagarde JP, Raisonnier A, Benlian P, Pritchard H, Hayden MR, Frohlich JJ. Abdel-Wareth LO, et al. Among authors: lagarde jp. Atherosclerosis. 1997 Dec;135(2):181-5. doi: 10.1016/s0021-9150(97)00159-7. Atherosclerosis. 1997. PMID: 9430367

5

High frequency of the apolipoprotein E *4 allele in African pygmies and most of the African populations in sub-Saharan Africa.

Zekraoui L, Lagarde JP, Raisonnier A, Gérard N, Aouizérate A, Lucotte G. Zekraoui L, et al. Among authors: lagarde jp. Hum Biol. 1997 Aug;69(4):575-81. Hum Biol. 1997. PMID: 9198315

6

A new informative Alw 26 I polymorphism in exon 10 of the human low density lipoprotein receptor gene. Application to prenatal diagnosis. Mutations in brief no. 145. Online.

Kottler M, Lagarde JP, Dahan K, Zekraoui L, Raisonnier A. Kottler M, et al. Among authors: lagarde jp. Hum Mutat. 1998;11(6):483. doi: 10.1002/(SICI)1098-1004(1998)11:6<483::AID-HUMU17>3.0.CO;2-5. Hum Mutat. 1998. PMID: 10200058

7

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

Bruckert E, Truffert J, De Gennes JL, Lagarde JP, Bernard C, Federspiel MC, Giral P, Dairou F. Bruckert E, et al. Among authors: lagarde jp. Clin Chim Acta. 1990 Apr 13;188(1):71-7. doi: 10.1016/0009-8981(90)90147-k. Clin Chim Acta. 1990. PMID: 2140732 No abstract available.

8

[Pseudo-hypertriglyceridemia caused by glycerol kinase deficiency].

Sanson-Raffin ML, Turpin G, Tzotzas T, Lagarde JP, Goussault Y, Cristini P, de Gennes JL. Sanson-Raffin ML, et al. Among authors: lagarde jp. Rev Med Interne. 1989 Sep-Oct;10(5):453-6. doi: 10.1016/s0248-8663(89)80052-9. Rev Med Interne. 1989. PMID: 2488489 Review. French. No abstract available.

9

Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa.

Souied EH, Benlian P, Rozet JM, Gerber S, Lagarde JP, Coscas G, Soubrane G, Duffier JL, Munnich A, Kaplan J. Souied EH, et al. Among authors: lagarde jp. Vision Res. 1998 Dec;38(24):3829-31. doi: 10.1016/s0042-6989(98)00176-x. Vision Res. 1998. PMID: 10211375 Free article.

10

The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration.

Souied EH, Benlian P, Amouyel P, Feingold J, Lagarde JP, Munnich A, Kaplan J, Coscas G, Soubrane G. Souied EH, et al. Among authors: lagarde jp. Am J Ophthalmol. 1998 Mar;125(3):353-9. doi: 10.1016/s0002-9394(99)80146-9. Am J Ophthalmol. 1998. PMID: 9512153

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