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Homa Ghabeli
20  Ergebnisse:
Personensuche X
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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/..
 
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2

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/..
 
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3

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/..
 
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4

Novel homozygous frameshift variant in the ATCAY gene in an..:

Siavashani, Elham Salehi ; Ashrafi, Mahmoud Reza ; Ghabeli, Homa..
BMC Medical Genomics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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5

Virtual and In-person Electroencephalography (EEG) Training..:

Mohammadi, Mahmoud ; Badv, Reza Shervin ; Zamani, Gholam Reza...
Iranian Journal of Pediatrics.  33 (2023)  4 - p. , 2023
Link: https://doi.org/10.5812/..
 
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6

Genetic Analysis of Forty MLPA-Negative Duchenne Muscular D..:

Zamani, Gholam Reza ; Mohammadi, Mohammad Farid ; Tavasoli, Ali Reza...
Journal of Molecular Neuroscience.  72 (2022)  5 - p. 1098-1107 , 2022
Link: https://doi.org/10.1007/..
 
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7

Epilepsia Partialis Continua a Clinical Feature of a Missen..:

Ashrafi, Mahmoud Reza ; Haghighi, Roya ; Badv, Reza Shervin...
Journal of Molecular Neuroscience.  72 (2022)  5 - p. 1125-1132 , 2022
Link: https://doi.org/10.1007/..
 
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8

The quality of life in children with spinal muscular atroph..:

Zamani, Gholamreza ; Ashrafi, Mahmoud Reza ; Ghabeli, Homa...
BMC Pediatrics.  22 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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9

Follow‐up of 25 patients with treatable ataxia: A comprehen..:

Ashrafi, Mahmoud Reza ; Pourbakhtyaran, Elham ; Rohani, Mohammad...
Clinical Case Reports.  10 (2022)  4 - p. , 2022
Link: https://doi.org/10.1002/..
 
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10

Primary and Secondary Microcephaly, Global Developmental De..:

Tavasoli, Ali Reza ; Memar, Elmira Haji Esmaeil ; Ashrafi, Mahmoud Reza...
Journal of Molecular Neuroscience.  72 (2022)  4 - p. 719-729 , 2022
Link: https://doi.org/10.1007/..
 
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11

Childhood Guillain–Barre syndrome in the SARS‐CoV‐2 era: Is..:

Pourbakhtyaran, Elham ; Heidari, Morteza ; Akbari, Masood Ghahvechi...
Clinical Case Reports.  10 (2022)  12 - p. , 2022
Link: https://doi.org/10.1002/..
 
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12

Novel homozygous frameshift variant in the ATCAY gene in an..:

Elham Salehi Siavashani ; Mahmoud Reza Ashrafi ; Homa Ghabeli..
https://doi.org/10.1186/s12920-023-01643-3.  , 2023
Link: https://doi.org/10.1186/..
 
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13

Childhood Guillain–Barre syndrome in the SARS‐CoV‐2 era: Is..:

Elham Pourbakhtyaran ; Morteza Heidari ; Masood Ghahvechi Akbari...
https://doi.org/10.1002/ccr3.6772.  , 2022
Link: https://doi.org/10.1002/..
 
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14

The quality of life in children with spinal muscular atroph..:

Gholamreza Zamani ; Mahmoud Reza Ashrafi ; Homa Ghabeli...
https://doi.org/10.1186/s12887-022-03751-y.  , 2022
Link: https://doi.org/10.1186/..
 
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15

Follow‐up of 25 patients with treatable ataxia: A comprehen..:

Mahmoud Reza Ashrafi ; Elham Pourbakhtyaran ; Mohammad Rohani...
https://doi.org/10.1002/ccr3.5777.  , 2022
Link: https://doi.org/10.1002/..
 
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