P.Y. Jeannet

Discipline

Psychologie (1) Education (1)

Type de document

Articles (7)

Co-auteur

Date

Source

Mot-clé

mutation (4) maladie (4) Patients (4) Human beings (4) Patients (4) Mutation (4) maladie (4) gène (3) Muscles--Diseases (3) enfant (2) Diagnosis (2) Development (2) Treatment (2) Cases (2) Therapeutics (2) Muscular dystrophy (2) Muscles (2) Diagnosis (2) Counseling (2) Cases (2) Skipping (2) roman (2) nourisson (1) puits (1) ventilation (1) thérapie (1) espèce (1) peau (1) risque (1) réflexion (1)

Documents écrit par P.Y. Jeannet (7) | parle de P.Y. Jeannet (0)

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
C.L. Bladen et al.
Enhanced excitation-coupled Ca(2+) entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease.
S. Treves et al. (2011)
Mitochondrial tRNA(Leu(UUR)) mutation m.3302A > G presenting as childhood-onset severe myopathy: threshold determination through segregation study.
D. Ballhausen et al. (2010)
Early onset collagen VI myopathies: Genetic and clinical correlations.
L. Briñas et al. (2010)
Considerations for prenatal counselling of patients with cardiac rhabdomyomas based on their cardiac and neurologic outcomes.
S.C. Degueldre et al. (2010)
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
M. Dunand et al.
The role of posterior fossa decompression in acute cerebellitis.
S. de Ribaupierre et al.