Suchergebnisse - "Moeinafshar, Aysan"

PubPharm (15)

1

Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

enthalten in: BMC medical genomics | 2024

von Ghasemi, M. | Tehrani Fateh, S. | Moeinafshar, A. | +13

2

Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

enthalten in: BMC medical genomics | 2024

von Ghasemi, M. | Tehrani Fateh, S. | Moeinafshar, A. | +13

3

Nephrectomy and IVC thrombectomy in renal cancer : a narrative review

enthalten in: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico | 2024

von Faegh, A. | Moeinafshar, A. | Rezaei, N.

4

Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors : current status and future directions

enthalten in: Cancer cell international | 2024

von Moeinafshar, A. | Nouri, M. | Shokrollahi, N. | +6

5

Circulating levels of inflammatory biomarkers in Huntington's disease : A systematic review and meta-analysis

enthalten in: Journal of neuroimmunology | 2023

von Soltani Khaboushan, A. | Moeinafshar, A. | Ersi, M. | +3

6

Alopecia areata-like pattern of baldness : the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2023

von Moeinafshar, A. | Tehrani Fateh, S. | Sadeghi, H. | +6

7

Genetically predicted smoking behaviors on Graves’ disease: A two-sample mendelian randomization

enthalten in: bioRxiv.org | 2023

von Akbarzadeh, M. | Pourganji, M. | Tabashiri, A. | +13

8

Genetically predicted 25-Hydroxyvitamin D levels on Hypothyroidism: A two-sample Mendelian Randomization

enthalten in: bioRxiv.org | 2023

von Akbarzadeh, M. | Fateh, S. | Moeinafshar, A. | +12

9

Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene

enthalten in: Neurological sciences | 2023

von Moeinafshar, A. | Tehrani Fateh, S. | Sadeghi, H. | +6

10

Clinical Functional Seizure Score (CFSS) : a simple algorithm for clinicians to suspect functional seizures

enthalten in: Frontiers in neurology | 2023

von Dashtkoohi, M. | Ranji-Bourachaloo, S. | Pouremamali, R. | +7