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Commissioning of the Iseult CEA 11.7 T whole-body MRI: current status, gradient–magnet interaction tests and first imaging experience.
Published in:
MAGMA: Magnetic Resonance Materials in Physics, Biology & Medicine, 2023, v. 36, n. 2, p. 175, doi. 10.1007/s10334-023-01063-5
By:
- Boulant, Nicolas;
- Quettier, Lionel;
- Aubert, G.;
- Amadon, A.;
- Belorgey, J.;
- Berriaud, C.;
- Bonnelye, C.;
- Bredy, Ph.;
- Chazel, E.;
- Dilasser, G.;
- Dubois, O.;
- Giacomini, E.;
- Gilgrass, G.;
- Gras, V.;
- Guihard, Q.;
- Jannot, V.;
- Juster, F. P.;
- Lannou, H.;
- Leprêtre, F.;
- Lerman, C.
Publication type:
Article
Monitoring of the microstructure of ion-irradiated nuclear ceramics by in situ Raman spectroscopy.
Published in:
Journal of Raman Spectroscopy, 2016, v. 47, n. 4, p. 476, doi. 10.1002/jrs.4837
By:
- Miro, S.;
- Bordas, E.;
- Thomé, L.;
- Costantini, J.‐M.;
- Leprêtre, F.;
- Trocellier, P.;
- Serruys, Y.;
- Beck, L.;
- Gosset, D.;
- Verlet, R.;
- Huguet‐Garcia, J.;
- Tupin, M.;
- Belleil, M.
Publication type:
Article
Waved aCGH: to smooth or not to smooth.
Published in:
Nucleic Acids Research, 2010, v. 38, n. 7, p. e94
By:
- Leprêtre, F.;
- Villenet, C.;
- Quief, S.;
- Nibourel, O.;
- Jacquemin, C.;
- Troussard, X.;
- Jardin, F.;
- Gibson, F.;
- Kerckaert, J. P.;
- Roumier, C.;
- Figeac, M.
Publication type:
Article
Molecular and cytogenetic characterisation of a small interstitial de novo 20p13→p12.3 deletion in a patient with severe growth deficit.
Published in:
Cytogenetics & Cell Genetics, 2001, v. 94, n. 3/4, p. 142, doi. 10.1159/000048806
By:
- Leprêtre, F.;
- Montpellier, A C.;
- Delannoy, V.;
- Froguel, P.;
- Vasseur, F.
Publication type:
Article
A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.
Published in:
2005
By:
- Siddiq A;
- Lepretre F;
- Hercberg S;
- Froguel P;
- Gibson F;
- Siddiq, Afshan;
- Lepretre, Frederic;
- Hercberg, Serge;
- Froguel, Philippe;
- Gibson, Fernando
Publication type:
journal article
Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients.
Published in:
1999
By:
- Otabe, Shuichi;
- Clement, Karine;
- Dubois, Severine;
- Lepretre, Frederic;
- Pelloux, Veronique;
- Leibel, Rudolph;
- Chung, Wendy;
- Boutin, Philippe;
- Guy-Grand, Bernard;
- Froguel, Philippe;
- Vasseur, Francis;
- Otabe, S;
- Clement, K;
- Dubois, S;
- Lepretre, F;
- Pelloux, V;
- Leibel, R;
- Chung, W;
- Boutin, P;
- Guy-Grand, B
Publication type:
journal article
Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation.
Published in:
Cytogenetic & Genome Research, 2003, v. 101, n. 2, p. 124, doi. 10.1159/000074167
By:
- Leprêtre, F.;
- Delannoy, V.;
- Froguel, P.;
- Vasseur, F.;
- Montepellier, C.
Publication type:
Article

Found: 7

Commissioning of the Iseult CEA 11.7 T whole-body MRI: current status, gradient–magnet interaction tests and first imaging experience.

Monitoring of the microstructure of ion-irradiated nuclear ceramics by in situ Raman spectroscopy.

Waved aCGH: to smooth or not to smooth.

Molecular and cytogenetic characterisation of a small interstitial de novo 20p13→p12.3 deletion in a patient with severe growth deficit.

A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.

Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients.

Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation.