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Search Results - Erogullari, A.
Search Results - Erogullari, A.
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P151 A homozygous THAP1 mutation as cause of early-onset generalized dystonia
by
Lohmann, K.
,
Ramirez, A.
,
Kaiser, F.J.
,
Shafiee, K.
,
Erogullari, A.
,
Brüggemann, N.
,
Winkler, S.
,
Bahman, I.
,
Osmanovic, A.
,
Shafa, M.
,
Bhatia, K.P.
,
Najmabadi, H.
,
Schneider, S.A.
,
Klein, C.
Published in
Basal ganglia
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The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6)
by
Kaiser, Frank J.
,
Osmanoric, Alma
,
Rakovic, Aleksandar
,
Erogullari, Alev
,
Uflacker, Nils
,
Braunholz, Diana
,
Lohnau, Thora
,
Orolicki, Slobodanka
,
Albrecht, Melanie
,
Gillessen-Kaesbach, Gabriele
,
Klein, Christine
,
Lohmann, Katja
Published in
Annals of neurology
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THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression
by
Erogullari, Alev
,
Hollstein, Ronja
,
Seibler, Philip
,
Braunholz, Diana
,
Koschmidder, Eva
,
Depping, Reinhard
,
Eckhold, Juliane
,
Lohnau, Thora
,
Gillessen-Kaesbach, Gabriele
,
Grünewald, Anne
,
Rakovic, Aleksandar
,
Lohmann, Katja
,
Kaiser, Frank J.
Published in
Biochimica et biophysica acta. Gene regulatory mechanisms
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Homozygous THAP1 mutations as cause of early-onset generalized dystonia
by
Schneider, Susanne A.
,
Ramirez, Alfredo
,
Shafiee, Kaveh
,
Kaiser, Frank J.
,
Erogullari, Alev
,
Brüggemann, Norbert
,
Winkler, Susen
,
Bahman, Ideh
,
Osmanovic, Alma
,
Shafa, Mohammad A.
,
Bhatia, Kailish P.
,
Najmabadi, Hossein
,
Klein, Christine
,
Lohmann, Katja
Published in
Movement disorders
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Identification and functional analysis of novel THAP1 mutations
by
Lohmann, Katja
,
Uflacker, Nils
,
Erogullari, Alev
,
Lohnau, Thora
,
Winkler, Susen
,
Dendorfer, Andreas
,
Schneider, Susanne A
,
Osmanovic, Alma
,
Svetel, Marina
,
Ferbert, Andreas
,
Zittel, Simone
,
Kühn, Andrea A
,
Schmidt, Alexander
,
Altenmüller, Eckart
,
Münchau, Alexander
,
Kamm, Christoph
,
Wittstock, Matthias
,
Kupsch, Andreas
,
Moro, Elena
,
Volkmann, Jens
,
Kostic, Vladimir
,
Kaiser, Frank J
,
Klein, Christine
,
Brüggemann, Norbert
Published in
European journal of human genetics : EJHG
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Truncating mutations in THAP1 define the nuclear localization signal
by
Osmanovic, Alma
,
Dendorfer, Andreas
,
Erogullari, Alev
,
Uflacker, Nils
,
Braunholz, Diana
,
Rakovic, Aleksandar
,
Vierke, Gudrun
,
Gil-Rodríguez, Conchi
,
Münchau, Alexander
,
Albrecht, Melanie
,
Brüggemann, Norbert
,
Gillessen-Kaesbach, Gabriele
,
Klein, Christine
,
Lohmann, Katja
,
Kaiser, Frank J.
Published in
Movement disorders
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Doppler ultrasonography versus venography in the detection of deep vein thrombosis in patients with pulmonary embolism
by
Ozbudak, Omer
,
Eroğullari, Ismail
,
Oğüş, Candan
,
Cilli, Aykut
,
Türkay, Mehtap
,
Ozdemir, Tülay
Published in
Journal of thrombosis and thrombolysis
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Lung Cancer Detection with Low-Dose Spiral Computed Tomography in Chronic Obstructive Pulmonary Disease Patients
by
Cilli, A.
,
Ozkaynak, C.
,
Onur, R.
,
Erogullari, I.
,
Ogus, C.
,
Cubuk, M.
,
Arslan, G.
,
Ozdemir, T.
Published in
Acta radiologica (1987)
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Doppler ultrasonography versus venography in the detection of deep vein thrombosis in patients with pulmonary embolism
by
Özbudak, Ömer
,
Eroğulları, Ismail
,
Öğüş, Candan
,
Çilli, Aykut
,
Türkay, Mehtap
,
Özdemir, Tülay
Published in
Journal of thrombosis and thrombolysis
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P419 Comparison of embletta portable device versus embla for diagnosing the obstructive sleep apnea
by
Cilli, Aykut
,
Erogullari, Ismail
,
Turhan, Murat
,
Ozbudak, Omer
,
Ozdemir, Tulay
,
Dinc, Oktay
Published in
Sleep medicine
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Journal Of Thrombosis And Thrombolysis
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Movement Disorders
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