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Moazzeni, Hamidreza
23  results:
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1

Identification of a mutation in TNRC18 in a patient with cl..:

Khani, Marzieh ; Shamshiri, Hosein ; Nafissi, Shahriar...
Clinical Case Reports.  12 (2024)  1 - p. , 2024
Link: https://doi.org/10.1002/..
 
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2

Identification of UBA1 as the causative gene of an X‐linked..:

Khani, Marzieh ; Nafissi, Shahriar ; Shamshiri, Hosein...
European Journal of Neurology.  29 (2022)  12 - p. 3556-3563 , 2022
Link: https://doi.org/10.1111/..
 
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3

A case of adult onset Sandhoff disease that mimics Brown-Vi..:

Khani, Marzieh ; Shamshiri, Hosein ; Moazzeni, Hamidreza...
Neuromuscular Disorders.  31 (2021)  6 - p. 528-531 , 2021
Link: https://doi.org/10.1016/..
 
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4

BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and T..:

Khani, Marzieh ; Shamshiri, Hosein ; Taheri, Hanieh...
Neurobiology of Aging.  99 (2021)  - p. 102.e1-102.e10 , 2021
Link: https://doi.org/10.1016/..
 
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5

Description of combined ARHSP/JALS phenotype in some patien..:

Khani, Marzieh ; Shamshiri, Hosein ; Fatehi, Farzad...
Molecular Genetics & Genomic Medicine.  8 (2020)  7 - p. , 2020
Link: https://doi.org/10.1002/..
 
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6

A Splicing Variant in OCRL Gene Might Explain the Second Ca..:

Houshmand, Massoud ; Babamohammadi, Gholamreza ; Moazzeni, Hamidreza..
Journal of Human Genetics and Genomics.  3 (2020)  1 - p. , 2020
Link: https://doi.org/10.5812/..
 
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7

Insights into the regulatory molecules involved in glaucoma..:

Moazzeni, Hamidreza ; Khani, Marzieh ; Elahi, Elahe
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  184 (2020)  3 - p. 782-827 , 2020
Link: https://doi.org/10.1002/..
 
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8

Deep geno- and phenotyping in two consanguineous families w..:

Khani, Marzieh ; Taheri, Hanieh ; Shamshiri, Hosein...
Journal of Neurology.  268 (2020)  2 - p. 640-650 , 2020
Link: https://doi.org/10.1007/..
 
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9

Identification of genes involved in glaucoma pathogenesis u..:

Moazzeni, Hamidreza ; Mirrahimi, Mehraban ; Moghadam, Abolfazl...
Human Molecular Genetics.  28 (2019)  21 - p. 3637-3663 , 2019
Link: https://doi.org/10.1093/..
 
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10

FMNL2 with functions related to the cytoskeleton is partial..:

Elahi, Elahe ; Ghorbanpour, Elham ; Pasalar, Parvin..
Journal of Ophthalmic and Vision Research.  12 (2017)  4 - p. 407 , 2017
Link: https://doi.org/10.4103/..
 
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11

Identification of direct target genes of miR-7, miR-9, miR-..:

Moazzeni, Hamidreza ; Najafi, Ali ; Khani, Marzieh
Molecular and Cellular Probes.  34 (2017)  - p. 45-52 , 2017
Link: https://doi.org/10.1016/..
 
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12

Expression of CXCL6 and BBS5 that may be glaucoma relevant ..:

Moazzeni, Hamidreza ; Akbari, Mohammad Taghi ; Yazdani, Shahin.
Gene.  593 (2016)  1 - p. 76-83 , 2016
Link: https://doi.org/10.1016/..
 
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13

Diagnosis of cystathionine beta-synthase deficiency by gene..:

Suri, Fatemeh ; Narooie-Nejad, Mehrnaz ; Safari, Iman...
Journal of the Neurological Sciences.  347 (2014)  1-2 - p. 305-309 , 2014
Link: https://doi.org/10.1016/..
 
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14

FOXC1 in human trabecular meshwork cells is involved in reg..:

Paylakhi, Seyed Hassan ; Moazzeni, Hamidreza ; Yazdani, Shahin...
Experimental Eye Research.  111 (2013)  - p. 112-121 , 2013
Link: https://doi.org/10.1016/..
 
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15

Description of combined ARHSP/JALS phenotype in some patien..:

Khani, Marzieh ; Shamshiri, Hosein ; Fatehi, Farzad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336765/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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