Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mehmet Ali Akalin"'
Autor:
Damla Çetinkaya Tezer, Melih Tutuncu, Mehmet Ali Akalin, Nurten Uzun, Feray Karaali Savrun, Meral E. Kiziltan, Aysegul Gunduz
Publikováno v:
Acta neurologica Belgica. 122(5)
Information regarding involuntary movements in chronic inflammatory polyneuropathy (CIDP) is gradually increasing. Our goal is to identify the types of involuntary movements in CIDP.All patients who were followed with the diagnosis of CIDP were invit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f31b4816a855fd18f6b1ff3febd0c889
https://pubmed.ncbi.nlm.nih.gov/35750953
https://pubmed.ncbi.nlm.nih.gov/35750953
Autor:
Mehmet Ali Akalin, Cemre Coşkun, Oznur Tastan, Tahsin Akgün, Ersin Tan, Aslihan Ozoguz Erimis, Mustafa Ertas, Halil Atilla Idrisoglu, Aysun Soysal, Erdi Şahin, Hamid Hamzeiy, Yesim Parman, Filiz Koç, Başar Bilgiç, Hasmet Hanagasi, Arman Çakar, Esra Gürsoy, Feza Deymeer, Ece Kartal, Fikret Aysal, Seyit Zor, Gulsen Babacan Yildiz, Nilda Turgut, Baris Isak, Gulden Olgun, Robin Palvadeau, Cemile Kocoglu, Fulya Akçimen, Tuncay Seker, Ersen Kavak, Elif Bayraktar, Utku Norman, A. Nazli Basak, A. Ercument Cicek, Ceren Tunca, Oguzhan Karakahya, Piraye Oflazer, Nesli-Ece Sen, Nurten Uzun Adatepe, Kayihan Uluc, Hacer Durmus, Cavit Boz, Dilcan Kotan
Publikováno v:
Human Mutation
Olgun, Gulden/0000-0002-4467-1610; Sahin, Erdi/0000-0002-5792-2888; Tastan, Oznur/0000-0001-7058-5372; Akcimen, Fulya/0000-0003-0931-5247; Kartal, Ece/0000-0002-7720-455X WOS:000542467300001 PubMed ID: 32579787 The last decade has proven that amyotro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54aef9b9d80c46be68614b3500ccd9db
http://hdl.handle.net/20.500.12645/18569
http://hdl.handle.net/20.500.12645/18569
Autor:
Filiz Koç, Burcu Gökçe Çokal, Tahir Kurtuluş Yoldaş, Zeynep Ünlütürk, Melih Tutuncu, Can Ebru Bekircan-Kurt, Ersin Tan, Cavit Boz, Berin Inan, Mehmet Ali Akalin, Sevim Erdem-Ozdamar, Necdet Karli, Abdülcemal Özcan, Kayihan Uluc, Özden Kamışlı, İhsan Şükrü Şengün, Duygu Guner Ozcanyuz, Selda Keskin, Onur Bulut, Hafize Nalan Güneş, Burhanettin Uludag, Çağdaş Erdoğan, Pinar Kahraman-Koytak
Publikováno v:
Archives of Neuropsychiatry
[No Abstract Available]
Peripheral Nerve Soc
Abdi Ibrahim Pharmaceuticals
This work was funded by Abdi Ibrahim Pharmaceuticals
Peripheral Nerve Soc
Abdi Ibrahim Pharmaceuticals
This work was funded by Abdi Ibrahim Pharmaceuticals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7a00bebf05fb4df3c23ea6bd8b0f33
https://hdl.handle.net/11454/70205
https://hdl.handle.net/11454/70205
Autor:
Sinem Yazici, Feray Karaali-Savrun, Aysegul Gunduz, Nurten Uzun, Mehmet Ali Akalin, Feray Bolukbasi, Gülsun Ersen, Meral E. Kiziltan
WOS:000468130500014 PubMed ID: 30911241 Introduction: We aimed to analyze the frequency, clinical characteristics, medical treatment options and final functional status of Guillain-Barre syndrome (GBS) and its variants in a population from a tertiary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5519d78f9ce862bfb9188995500da9b0
https://doi.org/10.5152/npa.2017.18091
https://doi.org/10.5152/npa.2017.18091
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 39(9)
Hereditary spastic paraparesis (HSP) constitutes both genetic and clinically heterogeneous group of upper motor neuron diseases. Half of the individuals with autosomal dominant (AD) HSP have mutations in SPAST, ATL1, and REEP1 genes. This study was c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42aacafcfe8b44b6a1ff82568e6e31c
https://pubmed.ncbi.nlm.nih.gov/29907907
https://pubmed.ncbi.nlm.nih.gov/29907907
Publikováno v:
Noro Psikiyatri Arsivi. 53:188-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19b0f36f7895fd7e78da8d646484c7f7
https://doi.org/10.5152/npa.2015.11310
https://doi.org/10.5152/npa.2015.11310
Autor:
Mehmet Ali Akalin, Leyla Kose, Metin Hallac, Meral E. Kiziltan, Aysegul Gunduz, Nurten Uzun, Mecbure Nalbantoglu
Publikováno v:
Muscle & Nerve. 51:936-938
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::484f7cf1afb0cb06611ad1cdb13be86e
https://doi.org/10.1002/mus.24610
https://doi.org/10.1002/mus.24610
Autor:
Amr H. Sawalha, Adam Adler, Yesim Gulsen-Parman, Mahdi Alahgholi-Hajibehzad, Alexander Marx, Oner Dogan, Feza Deymeer, Fikret Aysal, Piraye Oflazer, Güher Saruhan-Direskeneli, Vuslat Yilmaz, Travis K. Hughes, Mehmet Ali Akalin, Sibel P. Yentür, Hacer Durmus
This study aims to investigate genetic susceptibility to early-onset and late-onset anti-acetylcholine receptor antibody positive myasthenia gravis (EOMG and LOMG) and anti-muscle specific kinase antibody positive MG (MuSK-MG) at genome-wide level in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab41880803428b2e79e732068f87a876
https://aperta.ulakbim.gov.tr/record/56575
https://aperta.ulakbim.gov.tr/record/56575
Autor:
Feray Karaali-Savrun, Nurten Uzun, Aysegul Gunduz, Mehmet Ali Akalin, Melih Tutuncu, Meral E. Kiziltan
Publikováno v:
Clinical Neurophysiology. 129:e77
Introduction The reports on tremor and different types of polyneuropathies have been increasing and it was suggested to be associated with cerebellar involvement in chronic inflammatory demyelinating polyneuropathy (CIDP). Apart from specific syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c688c187a3bde97e35144591baa3e51
https://doi.org/10.1016/j.clinph.2018.04.190
https://doi.org/10.1016/j.clinph.2018.04.190
Autor:
Aslihan Ozoguz, Piraye Oflazer, Aslı Gündoğdu Eken, Feza Deymeer, Yesim Parman, Hacer Durmus, Peter C. Sapp, A. Nazli Basak, Halil Güllüoğlu, Filiz Koç, Murat Gunel, Fikret Aysal, Ozlem Keskin, Mehmet Ali Akalin, Başar Bilgiç, Suna Lahut, Tahsin Akgün, Dilcan Kotan, Özgün Uyan, Mustafa Ertas, Nilgün Döşoğlu, John Landers, Pinar Kavak, Mehmet Zarifoglu, Nesli-Ece Sen, Ceren Saygı, Kaya Bilguvar, Hakan Gurvit, Özgür Ömür, Robert H. Brown, Hasmet Hanagasi, Ersin Tan, Güneş Birdal, Zeynep Sena Agim, Hilmi Ozcelik, Pamela Keagle, Ceren Iskender, Ece Kartal
PubMedID: 25681989 The frequency of amyotrophic lateral sclerosis (ALS) mutations has been extensively investigated in several populations; however, a systematic analysis in Turkish cases has not been reported so far. In this study, we screened 477 A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73fbf09c47c098ca022a6efb77fbe36d
https://hdl.handle.net/20.500.12605/20890
https://hdl.handle.net/20.500.12605/20890