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Behavioral and Molecular Exploration of the AR-CMT2A Mouse Model Lmna.
Published in:
NeuroMolecular Medicine, 2012, v. 14, n. 1, p. 40, doi. 10.1007/s12017-012-8168-z
By:
- Poitelon, Yannick;
- Kozlov, Serguei;
- Devaux, Jerôme;
- Vallat, Jean-Michel;
- Jamon, Marc;
- Roubertoux, Pierre;
- Rabarimeriarijaona, Sitraka;
- Baudot, Cécile;
- Hamadouche, Tarik;
- Stewart, Colin;
- Levy, Nicolas;
- Delague, Valérie
Publication type:
Article
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 10, p. 1998
By:
- Lesage, Suzanne;
- Patin, Etienne;
- Condroyer, Christel;
- Leutenegger, Anne-Louise;
- Lohmann, Ebba;
- Giladi, Nir;
- Bar-Shira, Anat;
- Belarbi, Soraya;
- Hecham, Nassima;
- Pollak, Pierre;
- Ouvrard-Hernandez, Anne-Marie;
- Bardien, Soraya;
- Carr, Jonathan;
- Benhassine, Traki;
- Tomiyama, Hiroyuki;
- Pirkevi, Caroline;
- Hamadouche, Tarik;
- Cazeneuve, Cécile;
- Basak, A. Nazli;
- Hattori, Nobutaka
Publication type:
Article
Pantothenate kinase-associated neurodegeneration: Clinical description of 10 patients and identification of new mutations.
Published in:
Movement Disorders, 2011, v. 26, n. 9, p. 1777, doi. 10.1002/mds.23648
By:
- Assami, Salima;
- Azzedine, Hamid;
- Nouioua, Sonia;
- Mundwiller, Emeline;
- Mahoui, Soulaiman;
- Makri, Samira;
- Djemai, Meriam;
- Grid, Djamel;
- Brice, Alexis;
- Hamadouche, Tarik;
- Stevanin, Giovanni;
- Tazir, Meriem
Publication type:
Article
Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H)
Published in:
2012
By:
- Baudot, Cécile;
- Esteve, Clothilde;
- Castro, Christel;
- Poitelon, Yannick;
- Mas, Camille;
- Hamadouche, Tarik;
- El-Rajab, Maryam;
- Lévy, Nicolas;
- Megarbané, André;
- Delague, Valérie
Publication type:
Journal Article
Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H).
Published in:
Journal of the Peripheral Nervous System, 2012, v. 17, n. 2, p. 141, doi. 10.1111/j.1529-8027.2012.00405.x
By:
- Baudot, Cécile;
- Esteve, Clothilde;
- Castro, Christel;
- Poitelon, Yannick;
- Mas, Camille;
- Hamadouche, Tarik;
- El-Rajab, Maryam;
- Lévy, Nicolas;
- Megarbané, André;
- Delague, Valérie
Publication type:
Article
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Published in:
BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0180-3
By:
- Hamza, Wahiba;
- Pacha, Lamia Ali;
- Hamadouche, Tarik;
- Muller, Jean;
- Drouot, Nathalie;
- Ferrat, Farida;
- Makri, Samira;
- Chaouch, Malika;
- Tazir, Meriem;
- Koenig, Michel;
- Benhassine, Traki
Publication type:
Article

Found: 6

Behavioral and Molecular Exploration of the AR-CMT2A Mouse Model Lmna.

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

Pantothenate kinase-associated neurodegeneration: Clinical description of 10 patients and identification of new mutations.

Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H)

Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H).

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.