The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population by Mahdieh, Nejat, Heidari, Morteza, Rezaei, Zahra, Tavasoli, Ali Reza, Hosseinpour, Sareh, Rasulinejad, Maryam, Dehnavi, Ali Zare, Ghahvechi Akbari, Masoud, Badv, Reza Shervin, Vafaei, Elahe, Mohebbi, Ali, Mohammadi, Pouria, Hosseiny, Seyyed Mohammad Mahdi, Azizimalamiri, Reza, Nikkhah, Ali, Pourbakhtyaran, Elham, Rohani, Mohammad, Khanbanha, Narges, Nikbakht, Sedigheh, Movahedinia, Mojtaba, Karimi, Parviz, Ghabeli, Homa, Hosseini, Seyed Ahmad, Rashidi, Fatemeh Sadat, Garshasbi, Masoud, Kashani, Morteza Rezvani, Ghiasvand, Noor M, Zuchner, Stephan, Synofzik, Matthis, Ashrafi, Mahmoud Reza

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Phenotypic continuum of NFU1‐related disorders by Kaiyrzhanov, Rauan, Zaki, Maha S., Lau, Tracy, Sen, Sambuddha, Azizimalamiri, Reza, Zamani, Mina, Sayin, Gözde Yeşil, Hilander, Taru, Efthymiou, Stephanie, Chelban, Viorica, Brown, Ruth, Thompson, Kyle, Scarano, Maria Irene, Ganesh, Jaya, Koneev, Kairgali, Gülaçar, Ismail Musab, Person, Richard, Sadykova, Dinara, Maidyrov, Yerdan, Seifi, Tahereh, Zadagali, Aizhan, Bernard, Geneviève, Allis, Katrina, Elloumi, Houda Zghal, Lindy, Amanda, Taghiabadi, Ehsan, Verma, Sumit, Logan, Rachel, Kirmse, Brian, Bai, Renkui, Khalaf, Shaimaa M., Abdel‐Hamid, Mohamed S., Sedaghat, Alireza, Shariati, Gholamreza, Issa, Mahmoud, Zeighami, Jawaher, Elbendary, Hasnaa M., Brown, Garry, Taylor, Robert W., Galehdari, Hamid, Gleeson, Joseph J., Carroll, Christopher J., Cowan, James A., Moreno‐De‐Luca, Andres, Houlden, Henry, Maroofian, Reza

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Medication‐resistant acute focal motor seizures in a child with COVID‐19 affecting the CNS by Sadeghian, Saeid, Momen, Aliakbar, Jelodar, Gholamreza, Nasiri, Shahram, Azizimalamiri, Reza

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Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics by De Pace, Raffaella, Maroofian, Reza, Paimboeuf, Adeline, Zamani, Mina, Zaki, Maha S, Sadeghian, Saeid, Azizimalamiri, Reza, Galehdari, Hamid, Zeighami, Jawaher, Williamson, Chad D, Fleming, Emily, Zhou, Dihong, Gannon, Jennifer L, Thiffault, Isabelle, Roze, Emmanuel, Suri, Mohnish, Zifarelli, Giovanni, Bauer, Peter, Houlden, Henry, Severino, Mariasavina, Patten, Shunmoogum A, Farrow, Emily, Bonifacino, Juan S

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A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies by Hosseinpour, Sareh, Razmara, Ehsan, Heidari, Morteza, Rezaei, Zahra, Ashrafi, Mahmoud Reza, Dehnavi, Ali Zare, Kameli, Reyhaneh, Bereshneh, Ali Hosseini, Vahidnezhad, Hassan, Azizimalamiri, Reza, Zamani, Zahra, Pak, Neda, Rasulinezhad, Maryam, Mohammadi, Bahram, Ghabeli, Homa, Ghafouri, Mohammad, Mohammadi, Mahmoud, Zamani, Gholam Reza, Badv, Reza Shervin, Saket, Sasan, Rabbani, Bahareh, Mahdieh, Nejat, Ahani, Ali, Garshasbi, Masoud, Tavasoli, Ali Reza

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Impacts of the international economic sanctions on Iranian patients with epilepsy by Asadi-Pooya, Ali A., Azizimalamiri, Reza, Badv, Reza Shervin, Yarali, Bahram, Asadollahi, Marjan, Homayoun, Maryam, Sharifi, Samira

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Experimental Therapeutic Strategies in Epilepsies Using Anti-Seizure Medications by Rahim, Fakher, Azizimalamiri, Reza, Sayyah, Mehdi, Malayeri, Alireza

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ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations by Laugwitz, Lucia, Cheng, Fubo, Collins, Stephan C, Hustinx, Alexander, Navarro, Nicolas, Welsch, Simon, Cox, Helen, Hsieh, Tzung-Chien, Vijayananth, Aswinkumar, Buchert, Rebecca, Bender, Benjamin, Efthymiou, Stephanie, Murphy, David, Zafar, Faisal, Rana, Nuzhat, Grasshoff, Ute, Falb, Ruth J, Grimmel, Mona, Seibt, Annette, Zheng, Wenxu, Ghaedi, Hamid, Thirion, Marie, Couette, Sébastien, Azizimalamiri, Reza, Sadeghian, Saeid, Galehdari, Hamid, Zamani, Mina, Zeighami, Jawaher, Sedaghat, Alireza, Ramshe, Samira Molaei, Zare, Ali, Alipoor, Behnam, Klee, Dirk, Sturm, Marc, Ossowski, Stephan, Houlden, Henry, Riess, Olaf, Wieczorek, Dagmar, Gavin, Ryan, Maroofian, Reza, Krawitz, Peter, Yalcin, Binnaz, Distelmaier, Felix, Haack, Tobias B

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Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders by Ortigoza‐Escobar, Juan Darío, Zamani, Mina, Dorison, Nathalie, Sadeghian, Saeid, Azizimalamiri, Reza, Alvi, Javeria Raza, Sultan, Tipu, Galehdari, Hamid, Shariati, Gholamreza, Saberi, Alihossein, Leeuwen, Lisette, Zifarelli, Giovanni, Bauer, Peter, d'Hardemare, Vincent, Doummar, Diane, Roze, Emmanuel, Travaglini, Lorena, Nicita, Francesco, Ojea Ponce, Núria, Zahraei, Seyed Mohammadsaleh, Alabdi, Lama, Tamim, Abdullah, Hashem, Mais O., Ababneh, Faroug, Morrow, Michelle M, Curry, Cynthia, Tam, Allison, Ruedy, Jessica, Bhambhani, Vikas, Veith, Regan, Strømme, Petter, Efthymiou, Stephanie, Alkuraya, Fowzan S, Moreno‐De‐Luca, Andres, Burglen, Lydie, Houlden, Henry, Maroofian, Reza

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Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders by Maroofian, Reza, Kaiyrzhanov, Rauan, Cali, Elisa, Zamani, Mina, Zaki, Maha S, Ferla, Matteo, Tortora, Domenico, Sadeghian, Saeid, Saadi, Saadia Maryam, Abdullah, Uzma, Karimiani, Ehsan Ghayoor, Efthymiou, Stephanie, Yeşil, Gözde, Alavi, Shahryar, Al Shamsi, Aisha M, Tajsharghi, Homa, Abdel-Hamid, Mohamed S, Saadi, Nebal Waill, Al Mutairi, Fuad, Alabdi, Lama, Beetz, Christian, Ali, Zafar, Toosi, Mehran Beiraghi, Rudnik-Schöneborn, Sabine, Babaei, Meisam, Isohanni, Pirjo, Muhammad, Jameel, Khan, Sheraz, Al Shalan, Maha, Hickey, Scott E, Marom, Daphna, Elhanan, Emil, Kurian, Manju A, Marafi, Dana, Saberi, Alihossein, Hamid, Mohammad, Spaull, Robert, Meng, Linyan, Lalani, Seema, Maqbool, Shazia, Rahman, Fatima, Seeger, Jürgen, Palculict, Timothy Blake, Lau, Tracy, Murphy, David, Mencacci, Niccolo Emanuele, Steindl, Katharina, Begemann, Anais, Rauch, Anita, Akbas, Sinan, Aslanger, Ayça Dilruba, Salpietro, Vincenzo, Yousaf, Hammad, Ben-Shachar, Shay, Ejeskär, Katarina, Al Aqeel, Aida I, High, Frances A, Armstrong-Javors, Amy E, Zahraei, Seyed Mohammadsaleh, Seifi, Tahereh, Zeighami, Jawaher, Shariati, Gholamreza, Sedaghat, Alireza, Asl, Samaneh Noroozi, Shahrooei, Mohmmad, Zifarelli, Giovanni, Burglen, Lydie, Ravelli, Claudia, Zschocke, Johannes, Schatz, Ulrich A, Ghavideldarestani, Maryam, Kamel, Walaa A, Van Esch, Hilde, Hackenberg, Annette, Taylor, Jenny C, Al-Gazali, Lihadh, Bauer, Peter, Gleeson, Joseph J, Alkuraya, Fowzan Sami, Lupski, James R, Galehdari, Hamid, Azizimalamiri, Reza, Chung, Wendy K, Baig, Shahid Mahmood, Houlden, Henry, Severino, Mariasavina

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Putative founder effect of Arg338 AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families by Becker, Aurélie, Felici, Charlotte, Lambert, Laëtitia, Saint Martin, Anne, Abi‐Warde, Marie‐Thérèse, Schaefer, Elise, Zix, Christian, Zamani, Mina, Sadeghian, Saeid, Zeighami, Jawaher, Seifi, Tahereh, Azizimalamiri, Reza, Shariati, Gholamreza, Galehdari, Hamid, Selig, Mareike, Ding, Can, Duerinckx, Sarah, Pirson, Isabelle, Abramowicz, Marc, Clément, Guillemette, Leheup, Bruno, Jonveaux, Philippe, Lefort, Geneviève, Bronner, Myriam, Renaud, Mathilde, Bonnet, Céline

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High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry by Ashrafi, Mahmoudreza, Kameli, Reyhaneh, Hosseinpour, Sareh, Razmara, Ehsan, Zamani, Zahra, Rezaei, Zahra, Mashayekhi, Raziyeh, Pak, Neda, Barzegar, Mohammad, Azizimalamiri, Reza, Kashani, Morteza Rezvani, Khosroshahi, Nahideh, Rasulinezhad, Maryam, Heidari, Morteza, Amanat, Man, Abdi, Alireza, Mohammadi, Bahram, Mohammadi, Mahmoud, Zamani, Gholam Reza, Badv, Reza Shervin, Omrani, Abdolmajid, Nikbakht, Sedigheh, Bereshneh, Ali Hosseini, Movahedinia, Mojtaba, Moghaddam, Hossein Farshad, Ardakani, Hossein Shojaaldini, Akbari, Masood Ghahvechi, Tousi, Mehran Beiraghi, Shahi, Mohammad Vafaee, Hosseini, Firouzeh, Amouzadeh, Masoud Hassanvand, Hosseini, Seyed Ahmad, Nikkhah, Ali, Khajeh, Ali, Alizadeh, Hooman, Yarali, Bahram, Rohani, Mohammad, Karimi, Parviz, Elahi, Hadi Montazer Lotf, Hosseiny, Seyyed Mohamad Mahdi, Sadeghzadeh, Masoumeh Sadat, Mohebbi, Hossein, Moghadam, Maryam Hosseini, Aryan, Hajar, Vahidnezhad, Hassan, Soveizi, Mahdieh, Rabbani, Bahareh, Rabbani, Ali, Mahdieh, Nejat, Garshasbi, Masoud, Tavasoli, Ali Reza

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Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry by Ashrafi, Mahmoudreza, Kameli, Reyhaneh, Hosseinpour, Sareh, Razmara, Ehsan, Zamani, Zahra, Rezaei, Zahra, Mashayekhi, Raziyeh, Pak, Neda, Barzegar, Mohammad, Azizimalamiri, Reza, Kashani, Morteza Rezvani, Khosroshahi, Nahideh, Rasulinezhad, Maryam, Heidari, Morteza, Amanat, Man, Abdi, Alireza, Mohammadi, Bahram, Mohammadi, Mahmoud, Zamani, Gholam Reza, Badv, Reza Shervin, Omrani, Abdolmajid, Nikbakht, Sedigheh, Bereshneh, Ali Hosseini, Movahedinia, Mojtaba, Moghaddam, Hossein Farshad, Ardakani, Hossein Shojaaldini, Akbari, Masood Ghahvechi, Tousi, Mehran Beiraghi, Shahi, Mohammad Vafaee, Hosseini, Firouzeh, Amouzadeh, Masoud Hassanvand, Hosseini, Seyed Ahmad, Nikkhah, Ali, Khajeh, Ali, Alizadeh, Hooman, Yarali, Bahram, Rohani, Mohammad, Karimi, Parviz, Elahi, Hadi Montazer Lotf, Hosseiny, Seyyed Mohamad Mahdi, Sadeghzadeh, Masoumeh Sadat, Mohebbi, Hossein, Moghadam, Maryam Hosseini, Aryan, Hajar, Vahidnezhad, Hassan, Soveizi, Mahdieh, Rabbani, Bahareh, Rabbani, Ali, Mahdieh, Nejat, Garshasbi, Masoud, Tavasoli, Ali Reza

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We need well-designed multicenter studies to investigate neurologic manifestations of coronavirus disease 2019 by Ashrafi, Mahmoud Reza, Mohammadi, Mahmoud, Zamani, Gholamreza, Khosroshahi, Nahid, Shervin Badv, Reza, Tavasoli, Alireza, Heidari, Morteza, Yarali, Bahram, Azizimalamiri, Reza

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