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Morteza Heidari
385  Ergebnisse:
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1

Standards of Fluid Biomarker Collection and Pre-analytical ..:

Santorelli, Filippo M. ; McLoughlin, Hayley S. ; Wolter, Justin M....
The Cerebellum.  23 (2023)  3 - p. 881-886 , 2023
Link: https://doi.org/10.1007/..
 
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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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3

Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causin..:

Gilani, Naser ; Bitarafan, Fatemeh ; Ozaslan, Mehmet...
Molecular Genetics & Genomic Medicine.  12 (2024)  6 - p. , 2024
Link: https://doi.org/10.1002/..
 
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4

A Comprehensive Overview of NF1 Mutations in Iranian Patien..:

Savad, Shahram ; Modarressi, Mohammad-Hossein ; Younesi, Sarang...
NeuroMolecular Medicine.  26 (2024)  1 - p. , 2024
Link: https://doi.org/10.1007/..
 
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5

An overview of early-onset cerebellar ataxia: a practical g..:

Hosseinpour, Sareh ; Bemanalizadeh, Maryam ; Mohammadi, Pouria..
Acta Neurologica Belgica.  , 2024
Link: https://doi.org/10.1007/..
 
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6

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/..
 
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7

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/..
 
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8

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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9

Consensus Recommendations for Clinical Outcome Assessments ..:

Klockgether, Thomas ; Synofzik, Matthis ; Alhusaini, Saud...
The Cerebellum.  23 (2023)  3 - p. 924-930 , 2023
Link: https://doi.org/10.1007/..
 
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10

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/..
 
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11

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/..
 
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12

Incidence of neurological complications following pediatric..:

Abdshah, Alireza ; Mirzaaghayan, Mohammadreza ; Heidari, Morteza...
Health Science Reports.  6 (2023)  1 - p. , 2023
Link: https://doi.org/10.1002/..
 
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13

A comprehensive overview of SMN and NAIP copy numbers in Ir..:

Savad, Shahram ; Ashrafi, Mahmoud Reza ; Samadaian, Niusha...
Scientific Reports.  13 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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14

Correction to: High genetic heterogeneity of leukodystrophi..:

Ashrafi, Mahmoudreza ; Kameli, Reyhaneh ; Hosseinpour, Sareh...
neurogenetics.  24 (2023)  4 - p. 317-318 , 2023
Link: https://doi.org/10.1007/..
 
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15

Standards of NGS Data Sharing and Analysis in Ataxias: Reco..:

Beijer, Danique ; Fogel, Brent L. ; Beltran, Sergi...
The Cerebellum.  23 (2023)  2 - p. 391-400 , 2023
Link: https://doi.org/10.1007/..
 
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