E-LIB Suche - Ergebnisse für: ASHRAFZADEH, Farah

1

Transient blindness due to mild reversible encephalopathy i..:

Shekari, Shima ; Farsi, Farima ; Ashrafzadeh, Farah...
Clinical Case Reports. 12 (2024) 2 - p. , 2024

2

The diagnostic value of MRI findings in pediatric idiopathi..:

Seilanian Toosi, Farrokh ; Hashemi, Narges ; Emadzadeh, Maryam...
Child's Nervous System. 40 (2024) 7 - p. 2115-2123 , 2024

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

3

The prevalence of SMN gene deletion/duplication in spinal m..:

Shariati, Mohammad ; Davoudi, Alireza ; Boostani, Reza...
Egyptian Journal of Medical Human Genetics. 25 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

4

Motivation in caregiving among mothers of children with int..:

Hosseini, Seyed Javad ; Ramezani, Monir ; Ashrafzadeh, Farah.
BMC Pediatrics. 24 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

5

Correlation between Diagnostic Magnetic Resonance Imaging C..:

Beizaei, Behnam ; Toosi, Farrokh Seilanian ; Shahmoradi, Yousef...
Annals of Child Neurology. 32 (2024) 1 - p. 1-7 , 2024

Link: https://doi.org/10.26815..

6

Lunapark deficiency leads to an autosomal recessive neurode..:

Accogli, Andrea ; Zaki, Maha S ; Al-Owain, Mohammed...
Brain Communications. , 2023

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

7

Therapeutical impacts of transcranial direct current stimul..:

Ashrafzadeh, Farah ; Akhondian, Javad ; Hashemi, Narges...
Epilepsy Research. 190 (2023) - p. 107074 , 2023

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

8

Venous sinus stenting in pediatrics with normotensive pseud..:

Esmaeilzadeh, Mahla ; Hashemi, Narges ; Toosi, Mehran Beiraghi...
Journal of the Neurological Sciences. 455 (2023) - p. 121271 , 2023

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

9

Brain monoamine vesicular transport disease caused by homoz..:

Saida, Ken ; Maroofian, Reza ; Sengoku, Toru...
Genetics in Medicine. 25 (2023) 1 - p. 90-102 , 2023

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

10

Inherited deletion of 9p22.3‐p24.3 and duplication of 18p11..:

Ajami, Naser ; Kerachian, Mohammad Amin ; Toosi, Mehran Beiraghi...
Journal of Cellular and Molecular Medicine. 27 (2023) 4 - p. 496-505 , 2023

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

11

Clinico‐radiological features, molecular spectrum, and iden..:

Scala, Marcello ; Wortmann, Saskia B. ; Kaya, Namik...
Human Mutation. 43 (2022) 3 - p. 403-419 , 2022

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

12

Genotype–phenotype correlations and disease mechanisms in P..:

Borgia, Paola ; Baldassari, Simona ; Pedemonte, Nicoletta...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

13

TTC5syndrome: Clinical and molecular spectrum of a severe a..:

Musante, Luciana ; Faletra, Flavio ; Meier, Kolja...
American Journal of Medical Genetics Part A. 188 (2022) 9 - p. 2652-2665 , 2022

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

14

Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvat..:

Ghosh, Shereen G. ; Lee, Sangmoon ; Fabunan, Rudy...
Genetics in Medicine. 23 (2021) 3 - p. 524-533 , 2021

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

15

Comparison of birth weights of neonates of mothers receivin..:

Boskabadi, Hassan ; Maamouri, Gholamali ; Akhondian, Javad...
BMC Pregnancy and Childbirth. 21 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..