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Cirak, S.
110
results:
Articles (Online) X
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english (103)
german (5)
Sorted by: Relevance
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?
1
Clinical, electrophysiological and genetic characteristics ..:
Paketci, C.
;
Karakaya, M.
;
Edem, P.
...
Revue Neurologique. 176 (2020) 10 - p. 846-855 , 2020
Link:
https://doi.org/10.1016/..
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2
FV 49 Fast-myosin myopathy as a rare cause of external opht..:
Wunderlich, G.
;
Weis, J.
;
Kreutzer, M.
...
Clinical Neurophysiology. 130 (2019) 8 - p. e143 , 2019
Link:
https://doi.org/10.1016/..
?
3
Progrediente Dysarthrie, Ataxie, schmerzhafte Dysästhesien ..:
Petry-Schmelzer, J. N.
;
Cirak, S.
;
Kabbasch, C.
..
DGNeurologie. 2 (2019) 4 - p. 330-332 , 2019
Link:
https://doi.org/10.1007/..
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4
P.234Disruptive recessive TTN missense mutations cause a wi..:
Rees, M.
;
Fukuzawa, A.
;
Nikoopour, R.
...
Neuromuscular Disorders. 29 (2019) - p. S135 , 2019
Link:
https://doi.org/10.1016/..
?
5
Progrediente Dysarthrie, Ataxie, schmerzhafte Dysästhesien ..:
Petry-Schmelzer, J. N.
;
Cirak, S.
;
Kabbasch, C.
..
DGNeurologie. 2 (2019) 5 - p. 394-396 , 2019
Link:
https://doi.org/10.1007/..
?
6
Kongenitale myasthene Syndrome im Erwachsenenalter: Diagnos..:
Wunderlich, G.
;
Abicht, A.
;
Brunn, A.
...
Der Nervenarzt. 90 (2018) 2 - p. 148-159 , 2018
Link:
https://doi.org/10.1007/..
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7
Translational biochemistry for dystroglycanopathies:
Wang, H.
;
Sprute, R.
;
Daimagüler, H.
.
Neuromuscular Disorders. 27 (2017) - p. S109 , 2017
Link:
https://doi.org/10.1016/..
?
8
Severe form of recessive Charcot-Marie-Tooth disease with a..:
Bayram, A.
;
Stumpfe, K.
;
Wang, H.
...
Neuromuscular Disorders. 27 (2017) - p. S147 , 2017
Link:
https://doi.org/10.1016/..
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9
Recessively-acting choline transporter mutations associated..:
Wang, H.
;
Salter, S.
;
Refai, O.
...
Neuromuscular Disorders. 27 (2017) - p. S220-S221 , 2017
Link:
https://doi.org/10.1016/..
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10
Genetic Landscape of congenital myasthenic syndroms from Tu..:
Yiş, U.
;
Becker, K.
;
Kurul, S.
...
Neuromuscular Disorders. 27 (2017) - p. S221 , 2017
Link:
https://doi.org/10.1016/..
?
11
P 42 Congenital myasthenia in adult patients – a diagnostic..:
Ritter, C.
;
Cirak, S.
;
Abicht, A.
...
Clinical Neurophysiology. 128 (2017) 10 - p. e351 , 2017
Link:
https://doi.org/10.1016/..
?
12
Pediatric presentation of Marinesco–Sjögren syndrome with a..:
Kaçar Bayram, A.
;
Bayram, N.
;
Çırak, S.
...
Neuromuscular Disorders. 26 (2016) - p. S118 , 2016
Link:
https://doi.org/10.1016/..
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13
Neuroimaging signatures of alpha-dystroglycanopathies (ADG)..:
Ardicli, D.
;
Gocmen, R.
;
Cirak, S.
...
Neuromuscular Disorders. 26 (2016) - p. S163-S164 , 2016
Link:
https://doi.org/10.1016/..
?
14
A new homozygous frameshifting mutation in SPEG causes mild..:
Kaçar Bayram, A.
;
Per, H.
;
Zorludemir, S.
...
Neuromuscular Disorders. 26 (2016) - p. S117-S118 , 2016
Link:
https://doi.org/10.1016/..
?
15
Congenital mirror movements in alpha-dystroglycanopathy (AD..:
Ardicli, D.
;
Gocmen, R.
;
Cirak, S.
...
Neuromuscular Disorders. 26 (2016) - p. S165 , 2016
Link:
https://doi.org/10.1016/..
1-15