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Alavi, Afagh
78
results:
Search for persons
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Online (78)
Mediatypes
Articles (Online) (53)
OpenAccess-fulltext (25)
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english (73)
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1
A Novel Homozygous Variant in the MCOLN1 Gene Associated Wi..:
Ghasemi, Aida
;
Eslami Ardakani, Mahdieh
;
Togha, Mansoureh
...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. , 2024
Link:
https://doi.org/10.1017/..
?
2
Atypical presentations in an RTD patient and report of nove..:
Sabeghi, Donya
;
InanlooRahatloo, Kolsoum
;
Mirzadeh, Hanieh S.
...
Acta Neurologica Belgica. , 2024
Link:
https://doi.org/10.1007/..
?
3
Corrigendum to "NMNAT1 and hereditary spastic paraplegia (H..:
Sadr, Zahra
;
Ghasemi, Aida
;
Rohani, Mohammad
.
Neuromuscular Disorders. 35 (2024) - p. e1 , 2024
Link:
https://doi.org/10.1016/..
?
4
NMNAT1 and hereditary spastic paraplegia (HSP): expanding t..:
Sadr, Zahra
;
Ghasemi, Aida
;
Rohani, Mohammad
.
Neuromuscular Disorders. 33 (2023) 4 - p. 295-301 , 2023
Link:
https://doi.org/10.1016/..
?
5
Potential role of FKBP5 single‐nucleotide polymorphisms in ..:
Asadi‐Pooya, Ali A.
;
Simani, Leila
;
Asadollahi, Marjan
...
Epilepsia Open. 8 (2023) 2 - p. 479-486 , 2023
Link:
https://doi.org/10.1002/..
?
6
A new genetic variant, presenting as young onset rapidly pr..:
Eissazade, Negin
;
Alavi, Afagh
;
Lang, Anthony E.
...
Parkinsonism & Related Disorders. , 2023
Link:
https://doi.org/10.1016/..
?
7
Familial Hypermanganesemia in Iran:
Tabatabaee, Seyedeh Narges
;
Effat Nejad, Sajjad
;
Nikkhah, Ali
...
Movement Disorders Clinical Practice. 10 (2023) 5 - p. 850-853 , 2023
Link:
https://doi.org/10.1002/..
?
8
The first reports of FA2H-associated neurodegeneration from..:
Hashemi, Narges
;
Abadi, Reza Nejad Shahrokh
;
Alavi, Afagh
...
Neurological Sciences. 44 (2023) 12 - p. 4359-4362 , 2023
Link:
https://doi.org/10.1007/..
?
9
A founder mutation in COQ7, p.(Leu111Pro), causes pure here..:
Sadr, Zahra
;
Zare-Abdollahi, Davood
;
Rohani, Mohammad
.
Neurological Sciences. 44 (2023) 7 - p. 2599-2602 , 2023
Link:
https://doi.org/10.1007/..
?
10
White matter abnormalities in 15 subjects with SPG76:
Alkhalifa, Abdulrahman
;
Chen, Shihan
;
Hasiloglu, Zehra Isik
...
Journal of Neurology. 270 (2023) 12 - p. 5784-5792 , 2023
Link:
https://doi.org/10.1007/..
?
11
Estimation of Ambulation and Survival in Neurodegeneration ..:
Amini, Elahe
;
Rohani, Mohammad
;
Lang, Anthony E.
...
Movement Disorders Clinical Practice. 11 (2023) 1 - p. 53-62 , 2023
Link:
https://doi.org/10.1002/..
?
12
Identification of let-7f and miR-338 as plasma-based biomar..:
Daneshafrooz, Narges
;
Joghataei, Mohammad Taghi
;
Mehdizadeh, Mehdi
...
Scientific Reports. 12 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
13
The second family affected with a PRDM8-related disease:
Davarzani, Atefeh
;
Shahrokhi, Amin
;
Hashemi, Seyyed Saleh
...
Neurological Sciences. 43 (2022) 6 - p. 3847-3855 , 2022
Link:
https://doi.org/10.1007/..
?
14
Intellectual disability associated with craniofacial dysmor..:
Saghi, Mostafa
;
InanlooRahatloo, Kolsoum
;
Alavi, Afagh
..
BMC Medical Genomics. 15 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
15
White Matter Involvement in SPG76. A Retrospective MRI Anal..:
Alkhalifa, Abdulrahman
;
Chen, Shihan
;
Filosto, Massimiliano
...
Neurology. 98 (2022) 18_supplement - p. , 2022
Link:
https://doi.org/10.1212/..
1-15