E-LIB Suche - Ergebnisse für: Sedghi, Maryam

1

Genetic variant profiling of neonatal diabetes mellitus in ..:

Mianesaz, Hamidreza ; Ghalamkari, Safoura ; Abbasi, Farzaneh...
Journal of Diabetes Investigation. , 2024

Link: https://doi.org/10.1111/..

2

On genotype-phenotype relationshipof dystrophinopathies amo..:

Basiri, Keivan ; Alizadeh, Maryam ; Ansari, Behnaz...
Current Journal of Neurology. , 2023

Link: https://doi.org/10.18502..

3

Association of SOD2 rs2758339, rs5746136 and rs2842980 poly..:

Asadi, Sara ; Abkar, Morteza ; Zamanzadeh, Zahra...
Genes & Genomics. 45 (2023) 9 - p. 1165-1178 , 2023

Link: https://doi.org/10.1007/..

4

Causative variants linked with limb girdle muscular dystrop..:

Mianesaz, Hamidreza ; Ghalamkari, Safoura ; Salehi, Mansoor...
Molecular Genetics & Genomic Medicine. 11 (2022) 2 - p. , 2022

Link: https://doi.org/10.1002/..

5

How realistic is static traffic assignment? Analyzing autom..:

Mirzahossein, Hamid ; Gholampour, Iman ; Sedghi, Maryam.
Transportation Research Interdisciplinary Perspectives. 9 (2021) - p. 100320 , 2021

Link: https://doi.org/10.1016/..

6

An ancestral 10-bp repeat expansion in VWA1 causes recessiv..:

Pagnamenta, Alistair T ; Kaiyrzhanov, Rauan ; Zou, Yaqun...
Brain. 144 (2021) 2 - p. 584-600 , 2021

Link: https://doi.org/10.1093/..

7

Site selection methodology for emergency centers in Silk Ro..:

Mirzahossein, Hamid ; Sedghi, Maryam ; Motevalli Habibi, Hossein.
Innovative Infrastructure Solutions. 5 (2020) 3 - p. , 2020

Link: https://doi.org/10.1007/..

8

Understanding the impact of DIS3 cancer-associated mutation..:

Fazel, Esmat ; Fattahpour, Shirin ; Abdali, Hossein..
Gene Reports. 20 (2020) - p. 100779 , 2020

Link: https://doi.org/10.1016/..

9

Recessive Charcot-Marie-Tooth and multiple sclerosis associ..:

Sedghi, Maryam ; Moslemi, Ali-Reza ; Cabrera-Serrano, Macarena...
Brain Communications. 1 (2019) 1 - p. , 2019

Link: https://doi.org/10.1093/..

10

Motor neuron diseases caused by a novel VRK1 variant – A ge..:

Sedghi, Maryam ; Moslemi, Ali‐Reza ; Olive, Montse...
Annals of Clinical and Translational Neurology. 6 (2019) 11 - p. 2197-2204 , 2019

Link: https://doi.org/10.1002/..

11

A novel homozygous DPH1 mutation causes intellectual disabi..:

Sekiguchi, Futoshi ; Nasiri, Jafar ; Sedghi, Maryam...
Journal of Human Genetics. 63 (2018) 4 - p. 487-491 , 2018

Link: https://doi.org/10.1038/..

12

The role of scheme cognitive and emotional processing in th..:

Sedghi, Maryam ; Najafi, Soheila
Global Journal of Psychology Research: New Trends and Issues. 8 (2018) 3 - p. 107-116 , 2018

Link: https://doi.org/10.18844..

13

Association of AHSG with alopecia and mental retardation (A..:

Reza Sailani, M. ; Jahanbani, Fereshteh ; Nasiri, Jafar...
Human Genetics. 136 (2017) 3 - p. 287-296 , 2017

Link: https://doi.org/10.1007/..

14

D5S351 and D5S1414 located at the spinal muscular atrophy c..:

Sedghi, Maryam ; Vallian, Sadeq
Meta Gene. 7 (2016) - p. 16-19 , 2016

Link: https://doi.org/10.1016/..

15

Mutations inGMPPBcause congenital myasthenic syndrome and b..:

Belaya, Katsiaryna ; Rodríguez Cruz, Pedro M. ; Liu, Wei Wei...
Brain. 138 (2015) 9 - p. 2493-2504 , 2015

Link: https://doi.org/10.1093/..