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Author/Creator Leturcq, F

1. Improved cardiac outcomes by early treatment with angiotensin-converting enzyme inhibitors in becker muscular dystrophy. (14th October 2021)

Authors:
Motte, L; Stalens, C; Behin, A; Ben Yaou, R; Leturcq, F; Bassez, G; Laforet, P; Fontaine, B; Ederhy, S; Masingue, M; Saadi, M; Leonard Louis, S; Berber, N; Duboc, D; Wahbi, K
Journal:
European heart journal
Issue:
Volume 42(2021)Supplement 1
Page Start:
Record Type:
Journal Article
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2. Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa. Issue 4 (April 1994)

Authors:
el Kerch, F; Sefiani, A; Azibi, K; Boutaleb, N; Yahyaoui, M; Bentahila, A; Vinet, M C; Leturcq, F; Bachner, L; Beckmann, J
Journal:
Journal of medical genetics
Issue:
Volume 31:Issue 4(1994)
Page Start:
342
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Issue 6 (June 1997)

Authors:
Carrié, A; Piccolo, F; Leturcq, F; de Toma, C; Azibi, K; Beldjord, C; Vallat, J M; Merlini, L; Voit, T; Sewry, C; Urtizberea, J A; Romero, N; Tomé, F M; Fardeau, M; Sunada, Y; Campbell, K P; Kaplan, J C; Jeanpierre, M
Journal:
Journal of medical genetics
Issue:
Volume 34:Issue 6(1997)
Page Start:
470
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗