Tanya Stojkovic

发表

PHENOTYPE OF A PATIENT WITH RECESSIVE CENTRONUCLEAR MYOPATHY AND A NOVEL BIN1 MUTATION

K. Claeys, N. Romero, R. Carlier, 2010, Neurology.

Pregnancy in congenital myasthenic syndrome

L. Servais, B. Eymard, T. Stojkovic, 2013, Journal of Neurology.

Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations

B. Eymard, T. Stojkovic, T. Kuntzer, 2012, Neuromuscular Disorders.

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

D. Orlikowski, L. Viollet, B. Eymard, 2010, Journal of Neurology.

Muscle diseases with prominent joint contractures: Main entities and diagnostic strategy.

B. Eymard, T. Stojkovic, A. Ferreiro, 2013, Revue neurologique.

Upper limb onset of hereditary transthyretin amyloidosis is common in non‐endemic areas

C. Lacroix, P. Lozeron, V. Algalarrondo, 2018, European journal of neurology.

ColVI myopathies: where do we stand, where do we go?

T. Stojkovic, S. Quijano-roy, P. Richard, 2011, Skeletal Muscle.

The first European family with tibial muscular dystrophy outside the Finnish population

P. Vermersch, H. Petit, T. Stojkovic, 1998, Neurology.

[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience].

A. Béhin, D. Hantaı̈, T. Stojkovic, 2013, Revue neurologique.