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From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
Eur J Med Genet. 2015 Sep;58(9):443-54. doi: 10.1016/j.ejmg.2015.06.007. Epub 2015 Jul 17.
Eur J Med Genet. 2015.
PMID: 26193382
Bilateral cataract and high serum ferritin: a new dominant genetic disorder?
Bonneau D, Winter-Fuseau I, Loiseau MN, Amati P, Berthier M, Oriot D, Beaumont C.
Bonneau D, et al. Among authors: loiseau mn.
J Med Genet. 1995 Oct;32(10):778-9. doi: 10.1136/jmg.32.10.778.
J Med Genet. 1995.
PMID: 8558554
Free PMC article.
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Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract.
Beaumont C, Leneuve P, Devaux I, Scoazec JY, Berthier M, Loiseau MN, Grandchamp B, Bonneau D.
Beaumont C, et al. Among authors: loiseau mn.
Nat Genet. 1995 Dec;11(4):444-6. doi: 10.1038/ng1295-444.
Nat Genet. 1995.
PMID: 7493028
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Inhibitory effect of new imidazole derivatives on the proliferation and nucleic acid synthesis of leukemic cells.
Nafziger J, Guillosson JJ, Adam Y, Hecquet C, Payard M, Loiseau M.
Nafziger J, et al.
Cytotechnology. 1991 Jul;6(3):227-32. doi: 10.1007/BF00624761.
Cytotechnology. 1991.
PMID: 1370058
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Regioselective synthesis of substituted 3,4-dihydro-2H-thiines from alpha,beta-unsaturated oxathiolanes and styrene derivatives.
Kerverdo S, Loiseau M, Lizzani-Cuvelier L, Duñach E.
Kerverdo S, et al.
Chem Commun (Camb). 2001 Nov 7;(21):2284-5. doi: 10.1039/b106882m.
Chem Commun (Camb). 2001.
PMID: 12240152
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