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Burgunder,Jean-Marc

rp00012

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Full Name
Burgunder,Jean-Marc
(not current staff)
Variants
Burgunder, J.-M.
Jean-Marc, B.
 
Main Affiliation
 
Faculty
 
Email
mdcbjm@nus.edu.sg
 

Publications

Refined By:
Date Issued:  [2000 TO 2023]

Results 1-20 of 27 (Search time: 0.009 seconds).

Issue DateTitleAuthor(s)
118-Nov-2008A novel dominant mutation of the Nav1.4 α-subunit domain i leading to sodium channel myotoniaPetitprez, S.; Tiab, L.; Chen, L.; Kappeler, L.; Rösler, K.M.; Schorderet, D.; Abriel, H.; Burgunder, J.-M. 
22007Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-handChang, S.Y. ; Yong, T.F.; Liang, M.C. ; Soong, T.W. ; Yu, C.Y.; Pletnikova, O.; Troncoso, J.; Burgunder, J.-M. 
3Jun-2004Disturbed trafficking of dystrophin and associated proteins in targetoid phenomena after chronic muscle denervationVon Fellenberg, A.; Lin, S.; Burgunder, J.-M. 
42006DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and WestJamora, R.D.G.; Tan, E.-K.; Tan, L.C.S.; Liu, C.-P.; Kathirvel, P.; Burgunder, J.-M. 
52008Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutationChan, Y.-C.; Wilder-Smith, E. ; Sharma, V.; Ong, B.K.C. ; Burgunder, J.-M. ; Chew, S.-E.; Lam-Mok-Sing, K.M.J. 
61-Jun-2003Hereditary spastic paraplegia: Clues from a rare disorder for a common problem?Burgunder, J.-M. ; Hunziker, W. 
72003Hereditary spastic paraplegia: Clues from a rare disorder for a common problem?Burgunder, J.-M. ; Hunziker, W.
81-Aug-2003Identification of the Drosophila melanogaster homolog of the human spastin geneKammermeier, L.; Spring, J.; Stierwald, M.; Burgunder, J.-M. ; Reichert, H.
92003Identification of the Drosophila melanogaster homolog of the human spastin geneKammermeier, L.; Spring, J.; Stierwald, M.; Reichert, H.; Burgunder, J.-M. 
102003Idiopathic myositisBurgunder, J.-M. 
112003Idiopathic myositisBurgunder, J.-M. 
1219-Sep-2008Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese populationZhang, Z.-J.; Burgunder, J.-M. ; An, X.-K.; Wu, Y.; Chen, W.-J.; Zhang, J.-H.; Wang, Y.-C.; Xu, Y.-M.; Gou, Y.-R.; Yuan, G.-G.; Mao, X.-Y.; Peng, R.
139-Sep-2004Localization of DJ-1 mRNA in the mouse brainShang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.Shang, H.; Lang, D.; Jean-Marc, B. ; Kaelin-Lang, A.
14Mar-2008LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland ChinaAn, X.-K.; Peng, R.; Li, T.; Burgunder, J.-M. ; Wu, Y.; Chen, W.-J.; Zhang, J.-H.; Wang, Y.-C.; Xu, Y.-M.; Gou, Y.-R.; Yuan, G.-G.; Zhang, Z.-J.
152008LRRK2 mutations are not frequent in Swiss patients with Parkinson's diseaseBurgunder, J.-M. ; Tan, E.K.; Wirthmuller, U.; Jung, H.H.
1615-Oct-2009LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland ChinaZhang, Z.; Burgunder, J.-M. ; An, X.; Wu, Y.; Chen, W.; Zhang, J.; Wang, Y.; Xu, Y.; Gou, Y.; Yuan, G.; Mao, X.; Peng, R.
17May-2005Modulation of parvalbumin expression in the motor cortex of parkinsonian ratsCapper-Loup, C.; Burgunder, J.-M. ; Kaelin-Lang, A.
182005Modulation of parvalbumin expression in the motor cortex of parkinsonian ratsCapper-Loup, C.; Burgunder, J.-M. ; Kaelin-Lang, A.
192003Molecular genetic investigations in muscle diseasesBurgunder, J.-M. 
202003Molecular genetic investigations in muscle diseasesBurgunder, J.-M.