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Cervical Artery Dissections in the Puerperium: Pathogenic Hypotheses Concerning Seven Observations.
Published in:
Cerebrovascular Diseases, 2000, v. 10, n. 2, p. 158, doi. 10.1159/000016047
By:
- de Bray, J.M.;
- Guillon, B.;
- Neau, J.P.;
- Bouilliat, J.;
- Ducrocq, X.;
- Saudeau, D.;
- Vincent, D.;
- Penisson-Besnier, I.;
- Pasco, A.;
- Dubas, F.
Publication type:
Article
Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements.
Published in:
Molecular Human Reproduction, 1997, v. 3, n. 9, p. 811, doi. 10.1093/molehr/3.9.811
By:
- Lestienne, P;
- Reynier, P;
- ChrÃ©tien, M F;
- Penisson-Besnier, I;
- MalthiÃ¨ry, Y;
- Rohmer, V
Publication type:
Article
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay.
Published in:
Clinical Genetics, 2007, v. 72, n. 6, p. 582, doi. 10.1111/j.1399-0004.2007.00906.x
By:
- Krahn, M.;
- Pécheux, C.;
- Chapon, F.;
- Béroud, C.;
- Drouin-Garraud, V.;
- Laforet, P.;
- Romero, N. B.;
- Penisson-Besnier, I.;
- Bernard, R.;
- Urtizberea, J. A.;
- Leturcq, F.;
- Lévy, N.
Publication type:
Article
Ocular motor deficits in oculopharyngeal muscular dystrophy.
Published in:
European Journal of Neurology, 2012, v. 19, n. 4, p. e38, doi. 10.1111/j.1468-1331.2011.03657.x
By:
- Gautier, D.;
- Pénisson-Besnier, I.;
- Rivaud-Péchoux, S.;
- Rabaute, C.;
- Milea, D.
Publication type:
Article
Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblings.
Published in:
1998
By:
- Pénisson-Besnier, Isabelle;
- Richard, Isabelle;
- Dubas, Frédéric;
- Beckmann, Jacques S.;
- Fardeau, Michel;
- Pénisson-Besnier, I;
- Richard, I;
- Dubas, F;
- Beckmann, J S;
- Fardeau, M
Publication type:
journal article
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Published in:
Annals of Neurology, 2000, v. 48, n. 2, p. 170, doi. 10.1002/1531-8249(200008)48:2<170::AID-ANA6>3.0.CO;2-J
By:
- Bonne, G.;
- Mercuri, E.;
- Muchir, A.;
- Urtizberea, A.;
- Bécane, H. M.;
- Recan, D.;
- Merlini, L.;
- Wehnert, M.;
- Boor, R.;
- Reuner, U.;
- Vorgerd, M.;
- Wicklein, E. M.;
- Eymard, B.;
- Duboc, D.;
- Penisson-Besnier, I.;
- Cuisset, J. M.;
- Ferrer, X.;
- Desguerre, I.;
- Lacombe, D.;
- Bushby, K.
Publication type:
Article

Found: 6

Cervical Artery Dissections in the Puerperium: Pathogenic Hypotheses Concerning Seven Observations.

Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements.

Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay.

Ocular motor deficits in oculopharyngeal muscular dystrophy.

Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblings.

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.