Sahand Tehrani Fateh

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 13

Top Topics

Urinary Tract Infection

Epithelial Mesenchymal Transition

Top Venues

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

BMC medical genomics

Cancer cell international

Biochemical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Nima Shokrollahi, Sahand Tehrani Fateh, Mohammad Nouri, Amirmohammad Behnam, Parinaz Moghimi, Hossein Sadeghi, Reza Mirfakhraie, Hassan Roudgari, Sanaz Jamshidi, Mohammad Miryounesi, Mohammad Reza Ghasemi
The first Iranian patient with You-Hoover-Fong syndrome and a review of the literature on 27 cases: expanding the genotypic and phenotypic spectrum. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (8) (2024)
Nima Shokrollahi, Sahand Tehrani Fateh, Mohammad Nouri, Amirmohammad Behnam, Parinaz Moghimi, Hossein Sadeghi, Reza Mirfakhraie, Hassan Roudgari, Sanaz Jamshidi, Mohammad Miryounesi, Mohammad Reza Ghasemi
The first Iranian patient with You-Hoover-Fong syndrome and a review of the literature on 27 cases: expanding the genotypic and phenotypic spectrum. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (8) (2024)
Nima Shokrollahi, Sahand Tehrani Fateh, Mohammad Nouri, Amirmohammad Behnam, Parinaz Moghimi, Hossein Sadeghi, Reza Mirfakhraie, Hassan Roudgari, Sanaz Jamshidi, Mohammad Miryounesi, Mohammad Reza Ghasemi
The first Iranian patient with You-Hoover-Fong syndrome and a review of the literature on 27 cases: expanding the genotypic and phenotypic spectrum. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Aysan Moeinafshar, Mohammad Nouri, Nima Shokrollahi, Mahdi Masrour, Amirmohammad Behnam, Sahand Tehrani Fateh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad Reza Ghasemi
Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions. Cancer cell international 24 (1) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Aysan Moeinafshar, Mohammad Nouri, Nima Shokrollahi, Mahdi Masrour, Amirmohammad Behnam, Sahand Tehrani Fateh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad Reza Ghasemi
Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions. Cancer cell international 24 (1) (2024)
Parinaz Moghimi, Feyzollah Hashemi-Gorji, Sanaz Jamshidi, Sahand Tehrani Fateh, Shadab Salehpour, Hossein Sadeghi, Fatemeh Norouzi Rostami, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad Reza Ghasemi
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort. Biochemical genetics (2024)
Aysan Moeinafshar, Mohammad Nouri, Nima Shokrollahi, Mahdi Masrour, Amirmohammad Behnam, Sahand Tehrani Fateh, Hossein Sadeghi, Mohammad Miryounesi, Mohammad Reza Ghasemi
Non-coding RNAs as potential therapeutic targets for receptor tyrosine kinase signaling in solid tumors: current status and future directions. Cancer cell international 24 (1) (2024)
Aysan Moeinafshar, Sahand Tehrani Fateh, Hossein Sadeghi, Parvaneh Karimzadeh, Reza Mirfakhraie, Feyzollah Hashemi-Gorji, Pegah Larki, Mohammad Miryounesi, Mohammad Reza Ghasemi
Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi
Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers. Clinical case reports 11 (10) (2023)
Sahand Tehrani Fateh, Saman Bagheri, Hossein Sadeghi, Shadab Salehpour, Fatemehsadat Fazeli Bavandpour, Behnia Sadeghi, Sanaz Jamshidi, Seyed Hassan Tonekaboni, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad Reza Ghasemi
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)