Morlé L - Search Results

1

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: morle l. 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

2

Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio.

Randon J, Miraglia del Giudice E, Bozon M, Perrotta S, De Vivo M, Iolascon A, Delaunay J, Morle L. Randon J, et al. Among authors: morle l. Br J Haematol. 1997 Mar;96(3):500-6. doi: 10.1046/j.1365-2141.1997.d01-2074.x. Br J Haematol. 1997. PMID: 9054656 Free article.

3

Ankyrin Bugey: a de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis.

Morlé L, Bozon M, Alloisio N, Vallier A, Hayette S, Pascal O, Monier D, Philippe N, Forget BG, Delaunay J. Morlé L, et al. Am J Hematol. 1997 Mar;54(3):242-8. doi: 10.1002/(sici)1096-8652(199703)54:3<242::aid-ajh11>3.0.co;2-f. Am J Hematol. 1997. PMID: 9067504 Free article.

4

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis.

Kanzaki A, Hayette S, Morlé L, Inoue F, Matsuyama R, Inoue T, Yawata A, Wada H, Vallier A, Alloisio N, Yawata Y, Delaunay J. Kanzaki A, et al. Among authors: morle l. Br J Haematol. 1997 Dec;99(3):522-30. doi: 10.1046/j.1365-2141.1997.4263231.x. Br J Haematol. 1997. PMID: 9401060 Free article.

5

High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.

Miraglia del Giudice E, Francese M, Nobili B, Morlé L, Cutillo S, Delaunay J, Perrotta S. Miraglia del Giudice E, et al. Among authors: morle l. J Pediatr. 1998 Jan;132(1):117-20. doi: 10.1016/s0022-3476(98)70495-0. J Pediatr. 1998. PMID: 9470011

6

Hereditary spherocytosis: from clinical to molecular defects.

Iolascon A, Miraglia del Giudice E, Perrotta S, Alloisio N, Morlé L, Delaunay J. Iolascon A, et al. Among authors: morle l. Haematologica. 1998 Mar;83(3):240-57. Haematologica. 1998. PMID: 9573679 Review.

7

Occurrence of the alpha I 22 Arg----His (CGT----CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis.

Baklouti F, Marechal J, Morle L, Alloisio N, Wilmotte R, Pothier B, Ducluzeau MT, Kastally R, Delaunay J. Baklouti F, et al. Among authors: morle l. Br J Haematol. 1991 May;78(1):108-13. doi: 10.1111/j.1365-2141.1991.tb04391.x. Br J Haematol. 1991. PMID: 2043465

8

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia.

Hayette S, Morle L, Bozon M, Ghanem A, Risinger M, Korsgren C, Tanner MJ, Fattoum S, Cohen CM, Delaunay J. Hayette S, et al. Among authors: morle l. Br J Haematol. 1995 Apr;89(4):762-70. doi: 10.1111/j.1365-2141.1995.tb08413.x. Br J Haematol. 1995. PMID: 7772513

9

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.

Hayette S, Dhermy D, dos Santos ME, Bozon M, Drenckhahn D, Alloisio N, Texier P, Delaunay J, Morlé L. Hayette S, et al. Among authors: morle l. Blood. 1995 Jan 1;85(1):250-6. Blood. 1995. PMID: 7803799 Free article.

10

Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin.

Lorenzo F, Miraglia del Giudice E, Alloisio N, Morle L, Forissier A, Perrotta S, Sciarratta G, Iolascon A, Delaunay J. Lorenzo F, et al. Among authors: morle l. Br J Haematol. 1993 Jan;83(1):152-7. doi: 10.1111/j.1365-2141.1993.tb04646.x. Br J Haematol. 1993. PMID: 8435324

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