E-LIB Suche - Ergebnisse für: Emrahi, Leila

1

Two rare variants in the MYBPC3 gene associated with famili..:

Emrahi, Leila ; Hosseinzadeh, Hassan ; Tabrizi, Mehrnoush Toufan
Gene Reports. 26 (2022) - p. 101471 , 2022

2

The various regulatory functions of long noncoding RNAs in ..:

Heydarnezhad Asl, Mohammad ; Pasban Khelejani, Faezeh ; Bahojb Mahdavi, Seyedeh Zahra...
Journal of Cellular Biochemistry. 123 (2022) 6 - p. 995-1024 , 2022

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

3

Autosomal recessive cardiomyopathy and sudden cardiac death..:

Osborn, Daniel Peter Sayer ; Emrahi, Leila ; Clayton, Joshua...
Genetics in Medicine. 23 (2021) 4 - p. 787-792 , 2021

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

4

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/..

5

Expression study of CYP19A1 gene in a cohort of Iranian lei..:

Emrahi, Leila ; Behroozi, Javad ; Shahbazi, Shirin
Egyptian Journal of Medical Human Genetics. 19 (2018) 3 - p. 197-200 , 2018

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

6

Clinical utility of measuring expression levels of Stannioc..:

Hashemzadeh, Shahryar ; Arabzadeh, Amir Ahmad ; Estiar, Mehrdad Asghari...
Medical Oncology. 31 (2014) 10 - p. , 2014

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

7

Autosomal recessive cardiomyopathy and sudden cardiac death..:

Osborn, Daniel Peter Sayer ; Emrahi, Leila ; Clayton, Joshua...
Genetics in Medicine, 1098-3600, 2021, 23:4, s. 787-792. , 2021

Link: http://urn.kb.se/resolve..

8

Autosomal recessive cardiomyopathy and sudden cardiac death..:

Osborn, Daniel Peter Sayer ; Emrahi, Leila ; Clayton, Joshua...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026398/. , 2020

Link: http://www.ncbi.nlm.nih...

9

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

Sedghi, Maryam ; Moslemi, Ali‐Reza ; Olive, Montse...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856620/. , 2019

Link: http://www.ncbi.nlm.nih...

10

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

Sedghi, Maryam ; Moslemi, Ali‐Reza ; Olivé i Plana, Montserrat...
Reproducció del document publicat a: https://doi.org/10.1002/acn3.50912. , 2019

Link: http://hdl.handle.net/24..

11

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

Sedghi, Maryam ; Moslemi, Ali-Reza ; Olive, Montse...
Annals of Clinical and Translational Neurology, 2019, 6:11, s. 2197-2204. , 2019

Link: http://urn.kb.se/resolve..

12

New mutation in the NEBL gene in a family with Hypertrophic..:

Leila Emrahi ; Mehrnoush Toufan Tabrizi
https://mj.tbzmed.ac.ir/PDF/mj-43-323.pdf. , 2021

Link: https://doi.org/10.34172..

13

MYBPC3Δ25bp intronic deletion in hypertrophic cardiomyopath..:

Leila Emrahi ; Shirin Shahbazi ; Mehrnoush Toufan Tabrizi..
https://mj.tbzmed.ac.ir/PDF/mj-43-1-22.pdf. , 2021

Link: https://doi.org/10.34172..

14

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

Maryam Sedghi ; Ali‐Reza Moslemi ; Montse Olive...
https://doi.org/10.1002/acn3.50912. , 2019

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

15

Expression study of CYP19A1 gene in a cohort of Iranian lei..:

Leila Emrahi ; Javad Behroozi ; Shirin Shahbazi
http://www.sciencedirect.com/science/article/pii/S1110863017300873. , 2018

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