DASTSOOZ, Hassan

DASTSOOZ, Hassan  

SCIENZE DELLA VITA E BIOLOGIA DEI SISTEMI  

Risultati 1 - 11 di 11 (tempo di esecuzione: 0.015 secondi).
Titolo Data di pubblicazione Autore(i) File
Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy 2020 Habibzadeh P.; Silawi M.; Dastsooz H.; Bahramjahan S.; Ezzatzadegan Jahromi S.; Ostovan V.R.; Yavarian M.; Mofatteh M.; Faghihi M.A.
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: A case series 2019 Mahjoub G.; Habibzadeh P.; Dastsooz H.; Mirzaei M.; Kavosi A.; Jamali L.; Javanmardi H.; Katibeh P.; Faghihi M.A.; Dastgheib S.A.
A Comprehensive Bioinformatics Analysis of UBE2C in Cancers 2019 Dastsooz H.; Cereda M.; Donna D.; Oliviero S.
Expanding the molecular and clinical phenotypes of FUT8-CDG 2020 Ng B.G.; Dastsooz H.; Silawi M.; Habibzadeh P.; Jahan S.B.; Fard M.A.F.; Halliday B.J.; Raymond K.; Ruzhnikov M.R.Z.; Tabatabaei Z.; Taghipour-Sheshdeh A.; Brimble E.; Robertson S.P.; Faghihi M.A.; Freeze H.H.
Expression signature of lncRNA APTR in clinicopathology of breast cancer: Its potential oncogenic function in dysregulation of ErbB signaling pathway 2021 Mansoori, Hosein; Darbeheshti, Farzaneh; Daraei, Abdolreza; Mokhtari, Maral; Tabei, Mohammad Bagher; Abdollahzadeh, Rasoul; Dastsooz, Hassan; Bastami, Milad; Nariman-Saleh-Fam, Ziba; Salmani, Hamzeh; Mansoori, Yaser; Tahmasebi, Sedigheh
Investigating the association between common DRD2/ANKK1 genetic polymorphisms and schizophrenia: a meta-analysis 2021 Habibzadeh P; Nemati A; Dastsooz H; Taghipour-Sheshdeh A; Mariam Paul P; Sahraian A ; Faghihi MA.
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: A case report 2019 Zareifar S.; Dastsooz H.; Shahriari M.; Faghihi M.A.; Shekarkhar G.; Bordbar M.; Zekavat O.R.; Shakibazad N.
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: A Case report 2019 Ziyaee F.; Shorafa E.; Dastsooz H.; Habibzadeh P.; Nemati H.; Saeed A.; Silawi M.; Farazi Fard M.A.; Faghihi M.A.; Dastgheib S.A.
A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: A case report 2018 Esmaeilzadeh H.; Bordbar M.R.; Dastsooz H.; Silawi M.; Fard M.A.F.; Adib A.; Kafashan A.; Tabatabaei Z.; Sadeghipour F.; Faghihi M.A.
A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment 2019 Habibzadeh P.; Inaloo S.; Silawi M.; Dastsooz H.; Farazi Fard M.A.; Sadeghipour F.; Faghihi Z.; Rezaeian M.; Yavarian M.; Bohm J.; Faghihi M.A.
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia 2019 Farazi Fard M.A.; Rebelo A.P.; Buglo E.; Nemati H.; Dastsooz H.; Gehweiler I.; Reich S.; Reichbauer J.; Quintans B.; Ordonez-Ugalde A.; Cortese A.; Courel S.; Abreu L.; Powell E.; Danzi M.; Martuscelli N.B.; Bis-Brewer D.M.; Tao F.; Zarei F.; Habibzadeh P.; Yavarian M.; Modarresi F.; Silawi M.; Tabatabaei Z.; Yousefi M.; Farpour H.R.; Kessler C.; Mangold E.; Kobeleva X.; Mueller A.J.; Haack T.B.; Tarnopolsky M.; Gan-Or Z.; Rouleau G.A.; Synofzik M.; Sobrido M.-J.; Jordanova A.; Schule R.; Zuchner S.; Faghihi M.A.