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Homozygous PKP2 deletion associated with neonatal left ventricle noncompaction.
Published in:
Clinical Genetics, 2017, v. 91, n. 1, p. 126, doi. 10.1111/cge.12780
By:
- Ramond, F.;
- Janin, A.;
- Di Filippo, S.;
- Chanavat, V.;
- Chalabreysse, L.;
- Roux‐Buisson, N.;
- Sanlaville, D.;
- Touraine, R.;
- Millat, G.
Publication type:
Article
RNA splicing and editing modulation of 5-HT<sub>2C</sub> receptor function: relevance to anxiety and aggression in VGV mice.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 6, p. 656, doi. 10.1038/mp.2012.171
By:
- Martin, C B P;
- Ramond, F;
- Farrington, D T;
- Aguiar, A S;
- Chevarin, C;
- Berthiau, A-S;
- Caussanel, S;
- Lanfumey, L;
- Herrick-Davis, K;
- Hamon, M;
- Madjar, J J;
- Mongeau, R
Publication type:
Article
Diabetes Provides an Unfavorable Environment for Muscle Mass and Function after Muscle Injury in Mice.
Published in:
Pathobiology, 2007, v. 74, n. 5, p. 291, doi. 10.1159/000105812
By:
- Vignaud, A.;
- Ramond, F.;
- Hourdé, C.;
- Keller, A.;
- Butler-Browne, G.;
- Ferry, A.
Publication type:
Article
Detection of rare autosomal trisomies through non-invasive prenatal testing: benefits for pregnancy management.
Published in:
2019
By:
- Chatron, N.;
- Till, M.;
- Abel, C.;
- Bardel, C.;
- Ramond, F.;
- Sanlaville, D.;
- Schluth‐Bolard, C.;
- Schluth-Bolard, C
Publication type:
Letter
Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia.
Published in:
Journal of Neurology, 2024, v. 271, n. 9, p. 6038, doi. 10.1007/s00415-024-12574-z
By:
- Marelli, C.;
- Ramond, F.;
- Vignal, C.;
- Blanchet, C.;
- Frost, S.;
- Hao, Q.;
- Bocquet, B.;
- Nadjar, Y.;
- Leboucq, N.;
- Taieb, G.;
- Benkirane, M.;
- Hersent, C.;
- Koenig, M.;
- Meunier, I.
Publication type:
Article

Found: 5

Homozygous PKP2 deletion associated with neonatal left ventricle noncompaction.

RNA splicing and editing modulation of 5-HT<sub>2C</sub> receptor function: relevance to anxiety and aggression in VGV mice.

Diabetes Provides an Unfavorable Environment for Muscle Mass and Function after Muscle Injury in Mice.

Detection of rare autosomal trisomies through non-invasive prenatal testing: benefits for pregnancy management.

Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia.