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Search Results - Glumac, J. Nikodinović
Search Results - Glumac, J. Nikodinović
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A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
by
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
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Atypical peripheral manifestation of abnormal sphingolipid metabolism
by
MilicRasic, V
,
Atkinson, D
,
Nikodinovic Glumac, J
,
Jordanova, A
Published in
European journal of paediatric neurology
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Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies
by
Mladenović, J
,
Glumac, J. Nikodinović
,
Kosać, A
,
Marković, M. Keckarević
,
Baets, J
,
Rašić, V. Milić
Published in
Clinical neurophysiology
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P.81 - A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort
by
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
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CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.238The international database of titin gene variations and their phenotypes
by
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
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CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES
by
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
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Establishment of an international database of Titin mutations and their phenotypes – a follow up
by
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
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P.480 - Establishment of an international database of Titin mutations and their phenotypes – a follow up
by
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
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