Durou MR - Search Results

1

Functional characterization of sonic hedgehog mutations associated with holoprosencephaly.

Traiffort E, Dubourg C, Faure H, Rognan D, Odent S, Durou MR, David V, Ruat M. Traiffort E, et al. Among authors: durou mr. J Biol Chem. 2004 Oct 8;279(41):42889-97. doi: 10.1074/jbc.M405161200. Epub 2004 Jul 28. J Biol Chem. 2004. PMID: 15292211 Free article.

2

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.

Dubourg C, Lazaro L, Pasquier L, Bendavid C, Blayau M, Le Duff F, Durou MR, Odent S, David V. Dubourg C, et al. Among authors: durou mr. Hum Mutat. 2004 Jul;24(1):43-51. doi: 10.1002/humu.20056. Hum Mutat. 2004. PMID: 15221788

3

MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly.

Bendavid C, Dubourg C, Pasquier L, Gicquel I, Le Gallou S, Mottier S, Durou MR, Henry C, Odent S, David V. Bendavid C, et al. Among authors: durou mr. Hum Mutat. 2007 Dec;28(12):1189-97. doi: 10.1002/humu.20594. Hum Mutat. 2007. PMID: 17683084

4

Phenotypic and molecular variability of the holoprosencephalic spectrum.

Lazaro L, Dubourg C, Pasquier L, Le Duff F, Blayau M, Durou MR, de la Pintière AT, Aguilella C, David V, Odent S. Lazaro L, et al. Among authors: durou mr. Am J Med Genet A. 2004 Aug 15;129A(1):21-4. doi: 10.1002/ajmg.a.30110. Am J Med Genet A. 2004. PMID: 15266610

5

Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.

Bendavid C, Dubourg C, Gicquel I, Pasquier L, Saugier-Veber P, Durou MR, Jaillard S, Frébourg T, Haddad BR, Henry C, Odent S, David V. Bendavid C, et al. Among authors: durou mr. Hum Genet. 2006 Mar;119(1-2):1-8. doi: 10.1007/s00439-005-0097-6. Epub 2005 Dec 2. Hum Genet. 2006. PMID: 16323008

6

[Genetic study of holoprosencephaly].

Dubourg C, Lazaro L, Blayau M, Pasquier L, Durou MR, Odent S, David V. Dubourg C, et al. Among authors: durou mr. Ann Biol Clin (Paris). 2003 Nov-Dec;61(6):679-87. Ann Biol Clin (Paris). 2003. PMID: 14711609 Free article. French.

7

Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications.

Letellier C, Durou MR, Jouanolle AM, Le Gall JY, Poirier JY, Ruelland A. Letellier C, et al. Among authors: durou mr. Diabetes Metab. 2002 Sep;28(4 Pt 1):297-304. Diabetes Metab. 2002. PMID: 12442067

8

Determination of lipoprotein(a) concentrations and apolipoprotein(a) molecular weights in diabetic patients.

Ribault A, Durou MR, Letellier C, Wojcik F, Poirier JY, Ruelland A. Ribault A, et al. Among authors: durou mr. Diabetes Metab. 2000 Apr;26(2):107-12. Diabetes Metab. 2000. PMID: 10804324 Clinical Trial.

9

LDL sialic acid content in type 2 diabetic patients.

Ruelland A, Durou MR, Letellier C, Guehenneux E, Legras B, Allannic H, Cloarec L. Ruelland A, et al. Among authors: durou mr. Clin Chim Acta. 1997 Mar 18;259(1-2):191-3. doi: 10.1016/s0009-8981(96)06477-7. Clin Chim Acta. 1997. PMID: 9086308 No abstract available.

10

Fortuitous diagnosis of the association of hemoglobin J-Broussais with beta + thalassemia.

Durou MR, Ribault A, Dufour MJ, Gallou G, Ruelland A, Le Gall E, Cloarec L, Legras B. Durou MR, et al. Ann Biol Clin (Paris). 1996;54(8-9):321-3. Ann Biol Clin (Paris). 1996. PMID: 9092311

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13 results

Search Page

Filters