Vidaud M - Search Results

1

Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobins.

Rouyer-Fessard P, Plassa F, Blouquit Y, Vidaud M, Varnavides L, Mibashan RS, Bellingham A, Beuzard Y. Rouyer-Fessard P, et al. Among authors: vidaud m. Prenat Diagn. 1989 Jan;9(1):19-26. doi: 10.1002/pd.1970090104. Prenat Diagn. 1989. PMID: 2473467

2

Prenatal diagnosis of beta thalassaemia by reverse phase HPLC.

Rouyer-Fessard P, Beuzard Y, Vidaud M, John P, Mibashan RS. Rouyer-Fessard P, et al. Among authors: vidaud m. Prenat Diagn. 1987 Mar;7(3):171-8. doi: 10.1002/pd.1970070304. Prenat Diagn. 1987. PMID: 3588537

3

Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chains.

Rhoda MD, Domenget C, Vidaud M, Bardakdjian-Michau J, Rouyer-Fessard P, Rosa J, Beuzard Y. Rhoda MD, et al. Among authors: vidaud m. Biochim Biophys Acta. 1988 Jan 29;952(2):208-12. doi: 10.1016/0167-4838(88)90117-3. Biochim Biophys Acta. 1988. PMID: 3337825

4

Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemias.

Ghanem N, Vidaud M, Plassa F, Martin J, Goossens M. Ghanem N, et al. Among authors: vidaud m. Mol Cell Probes. 1993 Apr;7(2):167-8. doi: 10.1006/mcpr.1993.1024. Mol Cell Probes. 1993. PMID: 8321255

5

A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphisms.

Ghanem N, Girodon E, Vidaud M, Martin J, Fanen P, Plassa F, Goossens M. Ghanem N, et al. Among authors: vidaud m. Hum Mutat. 1992;1(3):229-39. doi: 10.1002/humu.1380010310. Hum Mutat. 1992. PMID: 1301930

6

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions.

Fanen P, Ghanem N, Vidaud M, Besmond C, Martin J, Costes B, Plassa F, Goossens M. Fanen P, et al. Among authors: vidaud m. Genomics. 1992 Jul;13(3):770-6. doi: 10.1016/0888-7543(92)90152-i. Genomics. 1992. PMID: 1379210

7

[Prenatal diagnosis of hemophilia A and B].

Vidaud M, Lavergne JM. Vidaud M, et al. Rev Prat. 1989 Dec 21;39(30):2689-96. Rev Prat. 1989. PMID: 2617062 French.

8

Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes.

Monplaisir N, Merault G, Poyart C, Rhoda MD, Craescu C, Vidaud M, Galacteros F, Blouquit Y, Rosa J. Monplaisir N, et al. Among authors: vidaud m. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9363-7. doi: 10.1073/pnas.83.24.9363. Proc Natl Acad Sci U S A. 1986. PMID: 3467311 Free PMC article.

9

The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene.

Pattinson JK, Millar DS, McVey JH, Grundy CB, Wieland K, Mibashan RS, Martinowitz U, Tan-Un K, Vidaud M, Goossens M, et al. Pattinson JK, et al. Among authors: vidaud m. Blood. 1990 Dec 1;76(11):2242-8. Blood. 1990. PMID: 1979502 Free article.

10

Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.

Girodon E, Ghanem N, Vidaud M, Riou J, Martin J, Galactéros F, Goossens M. Girodon E, et al. Among authors: vidaud m. Ann Hematol. 1992 Oct;65(4):188-92. doi: 10.1007/BF01703113. Ann Hematol. 1992. PMID: 1420507

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