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Tavasoli, Ali Reza
248
results:
Search for persons
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Format
Online (248)
Mediatypes
Articles (Online) (182)
Bookchapter (Online) (5)
OpenAccess-fulltext (61)
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english (228)
Sorted by: Relevance
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?
1
A comprehensive study of mutation and phenotypic heterogene..:
Hosseinpour, Sareh
;
Razmara, Ehsan
;
Heidari, Morteza
...
Brain and Development. 46 (2024) 4 - p. 167-179 , 2024
Link:
https://doi.org/10.1016/..
?
2
A comparative study on prophylactic efficacy of cinnarizine..:
Olfat, Mehrnaz
;
Hosseinpour, Sareh
;
Masoumi, Safdar
...
Cephalalgia. 44 (2024) 4 - p. , 2024
Link:
https://doi.org/10.1177/..
?
3
Distinct neurological phenotypes associated with biallelic ..:
Tasharrofi, Behnoosh
;
Najafi, Ali
;
Pourbakhtyaran, Elham
...
Molecular Biology Reports. 51 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
4
The genetic basis of early-onset hereditary ataxia in Iran:..:
Mahdieh, Nejat
;
Heidari, Morteza
;
Rezaei, Zahra
...
Human Genomics. 18 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
5
Identification of a Novel Homozygous GLS Gene Variant Assoc..:
Bazgir, Afsaneh
;
Agha Gholizadeh, Mehdi
;
Kahani, Seyyed Mohammad
..
Neurogenetics. , 2024
Link:
https://doi.org/10.1007/..
?
6
Normal Values of Nerve Conduction Studies in Children Aged ..:
Ghahvechi Akbari, Masood
;
Mahmoodpoor, Fazel
;
Ashrafi, Mahmoud Reza
...
Iranian Journal of Pediatrics. 33 (2023) 5 - p. , 2023
Link:
https://doi.org/10.5812/..
?
7
Phenotype and genotype heterogeneity of PLA2G6-associated n..:
Dehnavi, Ali Zare
;
Bemanalizadeh, Maryam
;
Kahani, Seyyed Mohammad
...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
8
Correction: Phenotype and genotype heterogeneity of PLA2G6-..:
Dehnavi, Ali Zare
;
Bemanalizadeh, Maryam
;
Kahani, Seyyed Mohammad
...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
9
Expanding phenotype heterogeneity of NARS2 by presenting su..:
Khodaeian, Mehrnoosh
;
Bitarafan, Fatemeh
;
Garrousi, Fatemeh
...
Journal of Clinical Laboratory Analysis. 37 (2023) 21-22 - p. , 2023
Link:
https://doi.org/10.1002/..
?
10
P366: Loss-of-function EGFR mutation in Bartter syndrome wi..:
Youssefian, Leila
;
Vahidnezhad, Hassan
;
Uitto, Jouni
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100394 , 2023
Link:
https://doi.org/10.1016/..
?
11
Phenotype and Genotype Heterogeneity of PLA2G6-associated N..:
Tavasoli, Ali Reza
;
Dehnavi, Ali Zare
;
Bemanalizadeh, Maryam
...
Neurology. 100 (2023) 17_supplement_2 - p. , 2023
Link:
https://doi.org/10.1212/..
?
12
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/..
?
13
Clinical and Genetic Characteristics of Limb-Girdle Muscula..:
Farshadmoghadam, Hossein
;
Zamani, Gholamreza
;
Ashrafi, Mahmoud Reza
..
Iranian Journal of Pediatrics. 33 (2023) 6 - p. , 2023
Link:
https://doi.org/10.5812/..
?
14
Expanding the neuroimaging findings of guanidinoacetate met..:
Afjei, Seyedeh Atiyeh
;
Mohammadi, Mohammad Farid
;
Pourbakhtyaran, Elham
...
neurogenetics. 24 (2023) 2 - p. 67-78 , 2023
Link:
https://doi.org/10.1007/..
?
15
Expanding the genetic spectrum of giant axonal neuropathy: ..:
Ashrafi, Mahmoud Reza
;
Dehnavi, Ali Zare
;
Tavasoli, Ali Reza
...
Molecular Genetics & Genomic Medicine. 11 (2023) 6 - p. , 2023
Link:
https://doi.org/10.1002/..
1-15