Molecular genetic investigations in muscle diseases

بواسطة Burgunder, J.-M.
منشور في 2016

Idiopathic myositis

بواسطة Burgunder, J.-M.
منشور في 2016

In vitro developmental expression of dystroglycan and laminin-α2 in human skeletal muscle

بواسطة Chen, L., Burgunder, J.-M.
منشور في 2016

Hereditary spastic paraplegia: Clues from a rare disorder for a common problem?

بواسطة Burgunder, J.-M., Hunziker, W.
منشور في 2016

Disturbed trafficking of dystrophin and associated proteins in targetoid phenomena after chronic muscle denervation

بواسطة Von Fellenberg, A., Lin, S., Burgunder, J.-M.
منشور في 2016

Modulation of parvalbumin expression in the motor cortex of parkinsonian rats

بواسطة Capper-Loup, C., Burgunder, J.-M., Kaelin-Lang, A.
منشور في 2014

Identification of the Drosophila melanogaster homolog of the human spastin gene

بواسطة Kammermeier, L., Spring, J., Stierwald, M., Burgunder, J.-M., Reichert, H.
منشور في 2016

LRRK2 mutations are not frequent in Swiss patients with Parkinson's disease

بواسطة Burgunder, J.-M., Tan, E.K., Wirthmuller, U., Jung, H.H.
منشور في 2011

Role of calcium-independent phospholipase A2in cortex striatum thalamus cortex circuitry-enzyme inhibition causes vacuous chewing movements in rats

بواسطة Lee, L.-Y., Ong, W.-Y., Burgunder, J.-M., Farooqui, A.A.
منشور في 2011

Very-late-onset Friedreich ataxia with disturbing head tremor and without spinal atrophy - A case report

بواسطة Galimanis, A., Glutz, L., Spiegel, R., Burgunder, J.-M., Kaelin-Lang, A.
منشور في 2011

Myotonia congenita-associated mutations in chloride channel-1 affect zebrafish body wave swimming kinematics

بواسطة Cheng W., Tian J., Burgunder J.-M., Hunziker W., Eng H.-L.
منشور في 2019

Role of phospholipase A2 in prepulse inhibition of the auditory startle reflex in rats

بواسطة Lee, L.-Y., Farooqui, A.A., Dawe, G.S., Burgunder, J.-M., Ong, W.-Y.
منشور في 2016

A novel dominant mutation of the Nav1.4 α-subunit domain i leading to sodium channel myotonia

بواسطة Petitprez, S., Tiab, L., Chen, L., Kappeler, L., Rösler, K.M., Schorderet, D., Abriel, H., Burgunder, J.-M.
منشور في 2015

DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West

بواسطة Jamora, R.D.G., Tan, E.-K., Tan, L.C.S., Liu, C.-P., Kathirvel, P., Burgunder, J.-M.
منشور في 2011

Spastin in the human and mouse central nervous system with special reference to its expression in the hippocampus of mouse pilocarpine model of status epilepticus and temporal lobe...

بواسطة Ma, D.L., Chia, S.C., Tang, Y.C., Chang, M.L.J., Tang, F.R., Probst, A., Burgunder, J.-M.
منشور في 2011

Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand

بواسطة Chang, S.Y., Yong, T.F., Liang, M.C., Soong, T.W., Yu, C.Y., Pletnikova, O., Troncoso, J., Burgunder, J.-M.
منشور في 2011

Association of GWAS loci with PD in China

بواسطة Chang, X.-L., Mao, X.-Y., Li, H.-H., Zhang, J.-H., Li, N.-N., Burgunder, J.-M., Peng, R., Tan, E.-K.
منشور في 2014

Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation

بواسطة Chan, Y.-C., Wilder-Smith, E., Sharma, V., Ong, B.K.C., Burgunder, J.-M., Chew, S.-E., Lam-Mok-Sing, K.M.J.
منشور في 2011

Functional parkin promoter polymorphism in Parkinson's disease: New data and meta-analysis

بواسطة Chang, X.-L., Mao, X.-Y., Li, H.-H., Zhang, J.-H., Li, N.-N., Burgunder, J.-M., Peng, R., Tan, E.-K.
منشور في 2014

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

بواسطة Zhang, Z., Burgunder, J.-M., An, X., Wu, Y., Chen, W., Zhang, J., Wang, Y., Xu, Y., Gou, Y., Yuan, G., Mao, X., Peng, R.
منشور في 2015