“Karoli xəstəliyi olan pasientdə hemorraqik insult, kliniki hal”, ATUREK, 2016 “Miller-Fişer sindromu, kliniki hal”, ATUREK, 2017 “Neuromyelitis optica xəstələyin diaqnostik kriteriyaları və differensial dianqostikası”, ATUREK, 2018 “Mono and polytherapy in treatment of patients with epilepsy” (Mahalov Sh.I., Khalilova D.M., Mursalova A.A; Oncology - XXI Century, Podgorica, Montenegro, April 29-May 5 2018); “GM1-Gangliosidosis Type III Associated Parkinsonism” ( Rauan Kaiyrzhanov, Ulviyya Guliyeva, Sughra Gulieva, Kamran Salayev, Aytan Mursalova, Parvin Allahyarova, Matteo P Ferla, Henry Houlden, September 3, 2021); “AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range” (Kamran Salayev, Clarissa Rocca, Rauan Kaiyrzhanov, Ulviyya Guliyeva, Sughra Guliyeva, Aytan Mursalova, Fatima Rahman, Najwa Anwar, Faisal Zafar, Farida Jan, Nuzhat Rana 6, Shazia Maqbool; SYNAPS Study Group; QUEEN SQUARE Genomics; Stephanie Efthymiou, Henry Houlden, November 2022).
“Karoli xəstəliyi olan pasientdə hemorraqik insult, kliniki hal”, ATUREK, 2016 “Miller-Fişer sindromu, kliniki hal”, ATUREK, 2017 “Neuromyelitis optica xəstələyin diaqnostik kriteriyaları və differensial dianqostikası”, ATUREK, 2018 “Mono and polytherapy in treatment of patients with epilepsy” (Mahalov Sh.I., Khalilova D.M., Mursalova A.A; Oncology - XXI Century, Podgorica, Montenegro, April 29-May 5 2018); “GM1-Gangliosidosis Type III Associated Parkinsonism” ( Rauan Kaiyrzhanov, Ulviyya Guliyeva, Sughra Gulieva, Kamran Salayev, Aytan Mursalova, Parvin Allahyarova, Matteo P Ferla, Henry Houlden, September 3, 2021); “AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range” (Kamran Salayev, Clarissa Rocca, Rauan Kaiyrzhanov, Ulviyya Guliyeva, Sughra Guliyeva, Aytan Mursalova, Fatima Rahman, Najwa Anwar, Faisal Zafar, Farida Jan, Nuzhat Rana 6, Shazia Maqbool; SYNAPS Study Group; QUEEN SQUARE Genomics; Stephanie Efthymiou, Henry Houlden, November 2022).
