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First results obtained in France with the latest model of the Fresenius cell separator: AS 104. [electronic resource] by
- Coffe, C
- Couteret, Y
- Devillers, M
- Fest, T
- Hervé, P
- Kieffer, Y
- Lamy, B
- Masse, M
- Morel, P
- Pouthier-Stein, F
Producer: 19930527
In:
Transfusion science vol. 14
Availability: No items available.
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Peripheral blood stem cell transplantation: approaches to an optimal blood stem cell collection. [electronic resource] by
- Coffe, C
- Couteret, Y
- Devillers, M
- Fest, T
- Morel, P
- Pouthier-Stein, F
- Calot, J P
- Novakovitch, G
- Sitthy, X
- Tremisi, P J
Producer: 19930325
In:
Transfusion science vol. 13
Availability: No items available.
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7.
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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. [electronic resource] by
- Verkarre, V
- Fournet, J C
- de Lonlay, P
- Gross-Morand, M S
- Devillers, M
- Rahier, J
- Brunelle, F
- Robert, J J
- Nihoul-Fékété, C
- Saudubray, J M
- Junien, C
Producer: 19981112
In:
The Journal of clinical investigation vol. 102
Availability: No items available.
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8.
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A PCSK9 variant and familial combined hyperlipidaemia. [electronic resource] by
- Abifadel, M
- Bernier, L
- Dubuc, G
- Nuel, G
- Rabès, J-P
- Bonneau, J
- Marques, A
- Marduel, M
- Devillers, M
- Munnich, A
- Erlich, D
- Varret, M
- Roy, M
- Davignon, J
- Boileau, C
Producer: 20090202
In:
Journal of medical genetics vol. 45
Availability: No items available.
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Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects. [electronic resource] by
- Saint-Jore, B
- Varret, M
- Dachet, C
- Rabès, J P
- Devillers, M
- Erlich, D
- Blanchard, P
- Krempf, M
- Mathé, D
- Chanu, B
- Jacotot, B
- Farnier, M
- Bonaïti-Péllié, C
- Junien, C
- Boileau, C
Producer: 20001207
In:
European journal of human genetics : EJHG vol. 8
Availability: No items available.
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Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11. [electronic resource] by
- Fournet, J C
- Mayaud, C
- de Lonlay, P
- Gross-Morand, M S
- Verkarre, V
- Castanet, M
- Devillers, M
- Rahier, J
- Brunelle, F
- Robert, J J
- Nihoul-Fékété, C
- Saudubray, J M
- Junien, C
Producer: 20010705
In:
The American journal of pathology vol. 158
Availability: No items available.
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11.
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A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32. [electronic resource] by
- Varret, M
- Rabès, J P
- Saint-Jore, B
- Cenarro, A
- Marinoni, J C
- Civeira, F
- Devillers, M
- Krempf, M
- Coulon, M
- Thiart, R
- Kotze, M J
- Schmidt, H
- Buzzi, J C
- Kostner, G M
- Bertolini, S
- Pocovi, M
- Rosa, A
- Farnier, M
- Martinez, M
- Junien, C
- Boileau, C
Producer: 19990520
In:
American journal of human genetics vol. 64
Availability: No items available.
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12.
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Dehydroepiandrosterone for myotonic dystrophy type 1. [electronic resource] by
- Pénisson-Besnier, I
- Devillers, M
- Porcher, R
- Orlikowski, D
- Doppler, V
- Desnuelle, C
- Ferrer, X
- Bes, M-C A
- Bouhour, F
- Tranchant, C
- Lagrange, E
- Vershueren, A
- Uzenot, D
- Cintas, P
- Solé, G
- Hogrel, J-Y
- Laforêt, P
- Vial, C
- Vila, A L
- Sacconi, S
- Pouget, J
- Eymard, B
- Chevret, S
- Annane, D
Producer: 20080812
In:
Neurology vol. 71
Availability: No items available.
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