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Search Results - Candayan, Ayşe
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Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages
by
Candayan, Ayşe
,
Parman, Yeşim
,
Battaloğlu, Esra
Published in
Balkan medical journal
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Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity
by
Kurolap, Alina
,
Kreuder, Florian
,
Gonzaga-Jauregui, Claudia
,
Duvdevani, Morasha Plesser
,
Harel, Tamar
,
Tammer, Luna
,
Xin, Baozhong
,
Bakhtiari, Somayeh
,
Rice, James
,
van Eyk, Clare L.
,
Gecz, Jozef
,
Mah, Jean K.
,
Atkinson, Derek
,
Cope, Heidi
,
Sullivan, Jennifer A.
,
Douek, Alon M.
,
Colquhoun, Daniel
,
Henry, Jason
,
Wlodkowic, Donald
,
Parman, Yesim
,
Candayan, Ayşe
,
Kocasoy-Orhan, Elif
,
Ilivitzki, Anat
,
Soudry, Shiri
,
Leibu, Rina
,
Glaser, Fabian
,
Sency, Valerie
,
Ast, Gil
,
Shashi, Vandana
,
Fahey, Michael C.
,
Battaloğlu, Esra
,
Jordanova, Albena
,
Meiner, Vardiella
,
Innes, A. Micheil
,
Wang, Heng
,
Elpeleg, Orly
,
Kruer, Michael C.
,
Kaslin, Jan
,
Baris Feldman, Hagit
Published in
American journal of human genetics
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Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia
by
Perić, Stojan
,
Marković, Vladana
,
Candayan, Ayşe
,
De Vriendt, Els
,
Momčilović, Nikola
,
Savić, Andrija
,
Dragašević-Mišković, Nataša
,
Svetel, Marina
,
Stević, Zorica
,
Božović, Ivo
,
Mesaroš, Šarlota
,
Drulović, Jelena
,
Basta, Ivana
,
Petrović, Igor
,
Tamaš, Olivera
,
Mijajlović, Milija
,
Novaković, Ivana
,
Sokić, Dragoslav
,
Jordanova, Albena
Published in
Cells (Basel, Switzerland)
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Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder
by
Çakar, Arman
,
İnci, Meltem
,
Özdağ Acarlı, Ayşe Nur
,
Çomu, Sinan
,
Candayan, Ayşe
,
Battaloğlu, Esra
,
Tekgül, Şeyma
,
Başak, Ayşe Nazlı
,
Durmuş, Hacer
,
Parman, Yeşim
Published in
Acta neurologica Scandinavica
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Identification and Characterization of Novel Founder Mutations in NDRG1: Refining the Genetic Landscape of Charcot–Marie–Tooth Disease Type 4D in Bulgaria
by
Atkinson, Derek
,
Chamova, Teodora
,
Candayan, Ayse
,
Kastreva, Kristina
,
Asenov, Ognian
,
Litvinenko, Ivan
,
Estrada-Cuzcano, Alejandro
,
Els De Vriendt
,
Kukushev, Georgi
,
Tournev, Ivailo
,
Jordanova, Albena
Published in
International journal of molecular sciences
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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype
by
Candayan, Ayşe
,
Yunisova, Gulshan
,
Çakar, Arman
,
Durmuş, Hacer
,
Başak, A. Nazlı
,
Parman, Yeşim
,
Battaloğlu, Esra
Published in
Neurogenetics
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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features
by
Çakar, Arman
,
Şahin, Erdi
,
Tezel, Seden
,
Candayan, Ayşe
,
Samancı, Bedia
,
Battaloğlu, Esra
,
Başak, A. Nazlı
,
Bilgiç, Başar
,
Hanağası, Haşmet
,
Durmuş, Hacer
,
Parman, Yeşim
Published in
Acta neurologica Belgica
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MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability
by
Ylikallio, Emil
,
Woldegebriel, Rosa
,
Tumiati, Manuela
,
Isohanni, Pirjo
,
Ryan, Monique M
,
Stark, Zornitza
,
Walsh, Maie
,
Sawyer, Sarah L
,
Bell, Katrina M
,
Oshlack, Alicia
,
Lockhart, Paul J
,
Shcherbii, Mariia
,
Estrada-Cuzcano, Alejandro
,
Atkinson, Derek
,
Hartley, Taila
,
Tetreault, Martine
,
Cuppen, Inge
,
van der Pol, W Ludo
,
Candayan, Ayse
,
Battaloglu, Esra
,
Parman, Yesim
,
van Gassen, Koen L I
,
van den Boogaard, Marie-José H
,
Boycott, Kym M
,
Kauppi, Liisa
,
Jordanova, Albena
,
Lönnqvist, Tuula
,
Tyynismaa, Henna
Published in
Brain (London, England : 1878)
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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort
by
Candayan, Ayşe
,
Çakar, Arman
,
Yunisova, Gulshan
,
Özdağ Acarlı, Ayşe Nur
,
Atkinson, Derek
,
Topaloğlu, Pınar
,
Durmuş, Hacer
,
Yapıcı, Zuhal
,
Jordanova, Albena
,
Parman, Yeşim
,
Battaloğlu, Esra
Published in
Neurology. Genetics
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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort
Published in
Neurology. Genetics
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