Arman Çakar (Çakar Arman, Arman Cakar)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 16

Top Venues

Brain : a journal of neurology

Brain communications

Amyotrophic lateral sclerosis & frontotemporal degeneration

Acta neurologica Belgica

This page only lists publications with an associated author ORCID identifier.

Publications

Reza Maroofian, Payam Sarraf, Thomas J O'Brien, Mona Kamel, Arman Çakar, Nour Elkhateeb, Tracy Lau, Siddaramappa Jagdish Patil, Christopher J Record, Alejandro Horga, Miriam Essid, Laila Selim, Hanene Benrhouma, Thouraya Ben Younes, Giovanni Zifarelli, Alistair T Pagnamenta, Peter Bauer, Mukhran Khundadze, Andrea Mirecki, Sara Mahmoud Kamel, Mohamed A Elmonem, Ehsan Ghayoor Karimiani, Yalda Jamshidi, Amaka C Offiah, Alexander M Rossor, Ilhem Ben Youssef-Turki, Christian A Hübner, Pinki Munot, Mary M Reilly, André E X Brown, Sara Nagy, Henry Houlden
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain : a journal of neurology 147 (7) (2024)
Arman Çakar, Reza Maroofian, Yesim Parman, Mary M Reilly, Henry Houlden
Novel and nano-rare genetic causes of paediatric-onset motor neuronopathies. Brain communications 6 (1) (2024)
Reza Maroofian, Payam Sarraf, Thomas J O'Brien, Mona Kamel, Arman Çakar, Nour Elkhateeb, Tracy Lau, Siddaramappa Jagdish Patil, Christopher J Record, Alejandro Horga, Miriam Essid, Laila Selim, Hanene Benrhouma, Thouraya Ben Younes, Giovanni Zifarelli, Alistair T Pagnamenta, Peter Bauer, Mukhran Khundadze, Andrea Mirecki, Sara Mahmoud Kamel, Mohamed A Elmonem, Ehsan Ghayoor Karimiani, Yalda Jamshidi, Amaka C Offiah, Alexander M Rossor, Ilhem Ben Youssef-Turki, Christian A Hübner, Pinki Munot, Mary M Reilly, André E X Brown, Sara Nagy, Henry Houlden
Reticulon 2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain : a journal of neurology (2024)
Arman Çakar, Reza Maroofian, Yesim Parman, Mary M Reilly, Henry Houlden
Novel and nano-rare genetic causes of paediatric-onset motor neuronopathies. Brain communications 6 (1) (2024)
Arman Çakar, Reza Maroofian, Yesim Parman, Mary M Reilly, Henry Houlden
Novel and nano-rare genetic causes of paediatric-onset motor neuronopathies. Brain communications 6 (1) (2024)
Reza Maroofian, Payam Sarraf, Thomas J O'Brien, Mona Kamel, Arman Çakar, Nour Elkhateeb, Tracy Lau, Siddaramappa Jagdish Patil, Christopher J Record, Alejandro Horga, Miriam Essid, Laila Selim, Hanene Benrhouma, Thouraya Ben Younes, Giovanni Zifarelli, Alistair T Pagnamenta, Peter Bauer, Mukhran Khundadze, Andrea Mirecki, Sara Mahmoud Kamel, Mohamed A Elmonem, Ehsan Ghayoor Karimiani, Yalda Jamshidi, Amaka C Offiah, Alexander M Rossor, Ilhem Ben Youssef-Turki, Christian A Hübner, Pinki Munot, Mary M Reilly, André E X Brown, Sara Nagy, Henry Houlden
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain : a journal of neurology 147 (7) (2024)
Reza Maroofian, Payam Sarraf, Thomas J O'Brien, Mona Kamel, Arman Çakar, Nour Elkhateeb, Tracy Lau, Siddaramappa Jagdish Patil, Christopher J Record, Alejandro Horga, Miriam Essid, Laila Selim, Hanene Benrhouma, Thouraya Ben Younes, Giovanni Zifarelli, Alistair T Pagnamenta, Peter Bauer, Mukhran Khundadze, Andrea Mirecki, Sara Mahmoud Kamel, Mohamed A Elmonem, Ehsan Ghayoor Karimiani, Yalda Jamshidi, Amaka C Offiah, Alexander M Rossor, Ilhem Ben Youssef-Turki, Christian A Hübner, Pinki Munot, Mary M Reilly, André E X Brown, Sara Nagy, Henry Houlden
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain : a journal of neurology 147 (7) (2024)
Arman Çakar, Kamaci Ibrahim, Orhan Kocasoy Elif, Durmuş Hacer, Parman Yeşim
Pembrolizumab-induced peripheral nervous system damage: A combination of myositis/ myasthenia overlap syndrome and motor axonal polyneuropathy. Ideggyogyaszati szemle 76 (11-12) (2023)
Arman Çakar, Gulandam Bagırova, Hacer Durmuş, Oya Uyguner, Yeşim Parman
Phenotypic features of RETREG1-related Hereditary Sensory Autonomic Neuropathy. Journal of the peripheral nervous system : JPNS (2023)
Arman Çakar, Emre Pekbilir, Serdar Ceylaner, Hacer Durmuş, Esra Battaloğlu, Umut Şahin, Yeşim Parman
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia. Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Arman Çakar, Emre Pekbilir, Serdar Ceylaner, Hacer Durmuş, Esra Battaloğlu, Umut Şahin, Yeşim Parman
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia. Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Annette Lischka, Katja Eggermann, Christopher J Record, Maike F Dohrn, Petra Laššuthová, Florian Kraft, Matthias Begemann, Daniela Dey, Eggermann Thomas, Danique Beijer, Jana Šoukalová, Matilde Laura, Alexander M Rossor, Radim Mazanec, Jonas Van Lent, Pedro José Tomaselli, Martin Ungelenk, Karlien Y Debus, Shawna M E Feely, Dieter Gläser, Sujatha Jagadeesh, Madelena Martin, Geeta M Govindaraj, Pratibha Singhi, Revanth Baineni, Niranjan Biswal, Marisol Ibarra-Ramírez, Maryse Bonduelle, Burkhard Gess, Juan Romero Sánchez, Renu Suthar, Vrajesh Udani, Atchayaram Nalini, Gopikrishnan Unnikrishnan, Wilson Marques Junior, Sandra Mercier, Vincent Procaccio, Céline Bris, Beena Suresh, Vaishnavi Reddy, Mariola Skorupinska, Nathalie Bonello-Palot, Fanny Mochel, Georg Dahl, Karthika Sasidharan, Fiji M Devassikutty, Sheela Nampoothiri, Maria J Rodovalho Doriqui, Wolfgang Müller-Felber, Katharina Vill, Tobias B Haack, Andreas Dufke, Michael Abele, Rolf Stucka, Saima Siddiqi, Noor Ullah, Stephanie Spranger, Deborah Chiabrando, Behiye S Bolgül, Yesim Parman, Pavel Seeman, Angelika Lampert, Jörg B Schulz, John N Wood, James J Cox, Michaela Auer-Grumbach, Vincent Timmerman, Jonathan de Winter, Andreas C Themistocleous, Michael Shy, David L H Bennett, Jonathan Baets, Christian A Hübner, Enrico Leipold, Stephan Züchner, Miriam Elbracht, Arman Çakar, Jan Senderek, Thorsten Hornemann, C Geoffrey Woods, Mary M Reilly, Ingo Kurth
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies. Brain : a journal of neurology (2023)
Arman Çakar, Meltem İnci, Ayşe Nur Özdağ Acarlı, Sinan Çomu, Ayşe Candayan, Esra Battaloğlu, Şeyma Tekgül, Ayşe Nazlı Başak, Hacer Durmuş, Yeşim Parman
Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder. Acta neurologica Scandinavica 145 (5) (2022)
Arman Çakar, Erdi Şahin, Seden Tezel, Ayşe Candayan, Bedia Samancı, Esra Battaloğlu, A Nazlı Başak, Başar Bilgiç, Haşmet Hanağası, Hacer Durmuş, Yeşim Parman
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features. Acta neurologica Belgica (2021)
Ayse Candayan, Arman Çakar, Gulshan Yunisova, Ayşe Nur Özdağ Acarli, Derek Atkinson, Pınar Topaloğlu, Hacer Durmuş, Zuhal Yapıcı, Albena Jordanova, Yeşim Parman, Esra Battaloğlu
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort. Neurology. Genetics 7 (5) (2021)
Arman Çakar, Halil İbrahim Akçay, Tuncay Gündüz, Murat Kürtüncü
Paraplegia following lumbar puncture: a rare complication in spinal dural arteriovenous fistula. Acta neurologica Belgica 118 (4) (2018)

Arman Çakar.css-eqlu8i{font-size:small;padding-left:4px;} (Çakar Arman, Arman Cakar)

Publication Activity (10 Years)

Top Topics

Top Venues

Arman Çakar (Çakar Arman, Arman Cakar)