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Common resistance mechanisms to deoxynucleoside analogues in variants of the human erythroleukaemic line K562.
Dumontet C, Fabianowska-Majewska K, Mantincic D, Callet Bauchu E, Tigaud I, Gandhi V, Lepoivre M, Peters GJ, Rolland MO, Wyczechowska D, Fang X, Gazzo S, Voorn DA, Vanier-Viornery A, MacKey J. Dumontet C, et al. Among authors: rolland mo. Br J Haematol. 1999 Jul;106(1):78-85. doi: 10.1046/j.1365-2141.1999.01509.x. Br J Haematol. 1999. PMID: 10444166 Free article.
Muscle phosphorylase b kinase deficiency revisited.
Echaniz-Laguna A, Akman HO, Mohr M, Tranchant C, Talmant-Verbist V, Rolland MO, Dimauro S. Echaniz-Laguna A, et al. Among authors: rolland mo. Neuromuscul Disord. 2010 Feb;20(2):125-7. doi: 10.1016/j.nmd.2009.11.004. Epub 2010 Jan 18. Neuromuscul Disord. 2010. PMID: 20080404
Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.
Harambat J, Fargue S, Acquaviva C, Gagnadoux MF, Janssen F, Liutkus A, Mourani C, Macher MA, Abramowicz D, Legendre C, Durrbach A, Tsimaratos M, Nivet H, Girardin E, Schott AM, Rolland MO, Cochat P. Harambat J, et al. Among authors: rolland mo. Kidney Int. 2010 Mar;77(5):443-9. doi: 10.1038/ki.2009.435. Epub 2009 Dec 16. Kidney Int. 2010. PMID: 20016466 Free article.
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder].
Pierron S, Giudicelli H, Moreigne M, Khalfi A, Touati G, Caruba C, Rolland MO, Acquaviva C. Pierron S, et al. Among authors: rolland mo. Arch Pediatr. 2010 Jan;17(1):10-3. doi: 10.1016/j.arcped.2009.09.022. Epub 2009 Nov 22. Arch Pediatr. 2010. PMID: 19932602 French.
94 results