A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
Topf, A, Nikodinović Glumac, J, Perić, S, Cassop-Thompson, M, Bertoli, M, Johnson, K, Phillips, L, MacArthur, D, Rakočević Stojanović, V, Straub, V
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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Atypical peripheral manifestation of abnormal sphingolipid metabolism
MilicRasic, V, Atkinson, D, Nikodinovic Glumac, J, Jordanova, A
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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P.81 - A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
Topf, A., Nikodinović Glumac, J., Perić, S., Cassop-Thompson, M., Bertoli, M., Johnson, K., Phillips, L., MacArthur, D., Rakočević Stojanović, V., Straub, V.
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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Journal Article
CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES
Hackman, P., Savarese, M., Bönnemann, C., Ferreiro, A., Beggs, A., Dawson, J., Thompson, R., Evangelista, T., Lochmüller, H., Nikodinovic Glumac, J., Jungbluth, H., Foye, S., Udd, B.
Published in Neuromuscular disorders : NMD (01.10.2018)
Published in Neuromuscular disorders : NMD (01.10.2018)
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CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.238The international database of titin gene variations and their phenotypes
Hackman, P., Savarese, M., Bönnemann, C., Ferreiro, A., Beggs, A., Dawson, J., Thompson, R., Evangelista, T., Lochmüller, H., Nikodinovic Glumac, J., Jungbluth, H., Foye, S., Udd, B.
Published in Neuromuscular disorders : NMD (01.10.2018)
Published in Neuromuscular disorders : NMD (01.10.2018)
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P.480 - Establishment of an international database of Titin mutations and their phenotypes – a follow up
Hackman, P., Savarese, M., Bönneman, C., Ferreiro, A., Beggs, A., Gautel, M., Davis, M., Evangelista, T., Glumac, J. Nikodinovic, Laporte, J., Smith, J., Richard, I., Granzier, H., Schneider, R., Jungbluth, H., Foye, S., Frase, A. Rockett, Udd, B.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
Establishment of an international database of Titin mutations and their phenotypes – a follow up
Hackman, P., Savarese, M., Bönneman, C., Ferreiro, A., Beggs, A., Gautel, M., Davis, M., Evangelista, T., Glumac, J. Nikodinovic, Laporte, J., Smith, J., Richard, I., Granzier, H., Schneider, R., Jungbluth, H., Foye, S., Frase, A. Rockett, Udd, B.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article