E-LIB Suche - Ergebnisse für: Yalda Nilipour

1

A compound heterozygote case of glutaric aciduria type II i..:

Seyedtaghia, Mohammad Reza ; Jafarzadeh‐Esfehani, Reza ; Hosseini, Seyedmojtaba...
Molecular Genetics & Genomic Medicine. 12 (2024) 7 - p. , 2024

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

2

A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in ..:

Hesami, Hamed ; Ghasemi, Serwa ; Houshmand, Golnaz...
BMC Musculoskeletal Disorders. 25 (2024) 1 - p. , 2024

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

3

Phenotypic and genotyping spectrum of two Iranian cases wit..:

Babaee, Marzieh ; Nilipour, Yalda ; Alijanpour, Sahar...
Neuropathology. , 2024

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

4

Neutral lipid storage disease with myopathy: clinicopatholo..:

Shahriyari, Hamed ; Ramezani, Mahtab ; Nilipour, Yalda...
Neuromuscular Disorders. 35 (2024) - p. 19-24 , 2024

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

5

A novel heterozygous missense MYH7 mutation potentially cau..:

Naderi, Niloofar ; Mohsen-Pour, Neda ; Nilipour, Yalda...
BMC Cardiovascular Disorders. 23 (2023) 1 - p. , 2023

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

6

Glioma Tumor Grading Using Radiomics on Conventional MRI: A..:

Moodi, Farzan ; Khodadadi Shoushtari, Fereshteh ; Ghadimi, Delaram J....
Journal of Magnetic Resonance Imaging. , 2023

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

7

Nemaline myopathy: reclassification of previously reported ..:

Haghighi, Alireza ; Alvandi, Zahra ; Nilipour, Yalda...
European Journal of Human Genetics. 31 (2023) 11 - p. 1237-1250 , 2023

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

8

Megaconial congenital muscular dystrophy due to CHKB gene v..:

Zemorshidi, Fariba ; Nafissi, Shahriar ; Boostani, Reza...
Neuromuscular Disorders. 33 (2023) 7 - p. 589-595 , 2023

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

9

Co‐occurrence of celiac disease and glycogen storage diseas..:

Khani, Sina ; Soheili, Amirali ; Vahabi, Seyed Mohammad...
Clinical Case Reports. 11 (2023) 8 - p. , 2023

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

10

Bi‐allelic loss of function variant in the NRCAM gene is as..:

Elahi, Zohreh ; Soveyzi, Mohamad ; Nafissi, Shahriar...
Molecular Genetics & Genomic Medicine. 11 (2023) 4 - p. , 2023

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

11

Two cases of inclusion body myositis presenting with unusua..:

Heidar, Matineh ; Nilipour, Yalda ; Hajiakhoundi, Fahimeh.
Current Journal of Neurology. , 2022

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

12

Recommendations for Infantile-Onset and Late-Onset Pompe Di..:

Fatehi, Farzad ; Ashrafi, Mahmoud Reza ; Babaee, Marzieh...
Frontiers in Neurology. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

13

Clinical and genetic spectrum of a large cohort of patients..:

Alonso-Pérez, Jorge ; González-Quereda, Lidia ; Bruno, Claudio...
Brain. 145 (2021) 2 - p. 596-606 , 2021

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

14

Sporadic late-onset nemaline myopathy with monoclonal gammo..:

Okhovat, Ali Asghar ; Nilipour, Yalda ; Boostani, Reza...
Neuromuscular Disorders. 31 (2021) 1 - p. 29-34 , 2021

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

15

Neurological Complications of COVID-19: A Rare Case of Bila..:

Safarpour Lima, Behnam ; Mohammadi Khorasani, Negar ; Aghamiri, Seyed Hossein..
The Journal of Emergency Medicine. 61 (2021) 6 - p. e160-e163 , 2021

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