Delaunay J - Search Results

1

Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.

del Giudice EM, Ducluzeau MT, Alloisio N, Wilmotte R, Delaunay J, Perrotta S, Cutillo S, Iolascon A. del Giudice EM, et al. Among authors: delaunay j. Hum Genet. 1992 Jul;89(5):553-6. doi: 10.1007/BF00219183. Hum Genet. 1992. PMID: 1353056

2

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74).

Perrotta S, Miraglia del Giudice E, Alloisio N, Sciarratta G, Pinto L, Delaunay J, Cutillo S, Iolascon A. Perrotta S, et al. Among authors: delaunay j. Blood. 1994 Jun 1;83(11):3346-9. Blood. 1994. PMID: 8193371 Free article.

3

An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphism.

Dalla Venezia N, Wilmotte R, Morlé L, Forissier A, Parquet N, Garbarz M, Rousset T, Dhermy D, Alloisio N, Delaunay J. Dalla Venezia N, et al. Among authors: delaunay j. Hum Genet. 1993 Feb;90(6):641-4. doi: 10.1007/BF00202482. Hum Genet. 1993. PMID: 8444470

4

Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.

Guetarni D, Roux AF, Alloisio N, Morlé F, Ducluzeau MT, Forget BG, Colonna P, Delaunay J, Godet J. Guetarni D, et al. Among authors: delaunay j. Hum Genet. 1990 Oct;85(6):627-30. doi: 10.1007/BF00193587. Hum Genet. 1990. PMID: 2227954

5

A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli.

Wilmotte R, Miraglia del Giudice E, Marechal J, Perrotta S, de Mattia D, Delaunay J, Iolascon A. Wilmotte R, et al. Among authors: delaunay j. Br J Haematol. 1994 Oct;88(2):437-9. doi: 10.1111/j.1365-2141.1994.tb05051.x. Br J Haematol. 1994. PMID: 7803301

6

Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis.

del Giudice EM, Hayette S, Bozon M, Perrotta S, Alloisio N, Vallier A, Iolascon A, Delaunay J, Morlé L. del Giudice EM, et al. Among authors: delaunay j. Br J Haematol. 1996 Jun;93(4):828-34. doi: 10.1046/j.1365-2141.1996.d01-1746.x. Br J Haematol. 1996. PMID: 8703812

7

Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.

Maillet P, Alloisio N, Morlé L, Delaunay J. Maillet P, et al. Among authors: delaunay j. Hum Mutat. 1996;8(2):97-107. doi: 10.1002/(SICI)1098-1004(1996)8:2<97::AID-HUMU1>3.0.CO;2-M. Hum Mutat. 1996. PMID: 8844207

8

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Carella M, Stewart G, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A. Carella M, et al. Among authors: delaunay j. Am J Hum Genet. 1998 Sep;63(3):810-6. doi: 10.1086/302024. Am J Hum Genet. 1998. PMID: 9718354 Free PMC article.

9

Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1.

Alloisio N, Dorléac E, Girot R, Delaunay J. Alloisio N, et al. Among authors: delaunay j. Hum Genet. 1981;59(1):68-71. doi: 10.1007/BF00278857. Hum Genet. 1981. PMID: 10819025

10

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution.

Pothier B, Alloisio N, Maréchal J, Morlé L, Ducluzeau MT, Caldani C, Philippe N, Delaunay J. Pothier B, et al. Among authors: delaunay j. Blood. 1990 May 15;75(10):2061-9. Blood. 1990. PMID: 2337674 Free article.

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