Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Parham Habibzadeh

Showing results (41-50 of 60) with videos related to

Pageof 6
Sort By:
Journal of Genetics|September 2, 2021
Investigating the association between common <i>DRD2/ANKK1</i> genetic polymorphisms and schizophrenia: a meta-analysisParham Habibzadeh, Azim Nemati, Hassan Dastsooz, et al.
BMC Medical Genetics|March 23, 2019
An immunocompetent patient with a nonsense mutation in NHEJ1 geneHossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, et al.
Biochemia Medica|August 11, 2020
Rate of re-positive RT-PCR test among patients recovered from COVID-19Parham Habibzadeh, Mohammad M Sajadi, Amir Emami, et al.
Cell Journal|November 27, 2021
Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in <i>DPAGT1</i> GeneZahra Tabatabaei, K Hadijeh Karbalaie, Parham Habibzadeh, et al.
BMC Gastroenterology|May 10, 2020
Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal EncephalomyopathyParham Habibzadeh, Mohammad Silawi, Hassan Dastsooz, et al.
BMC Medical Genetics|October 31, 2019
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case seriesGhazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, et al.
The Journal of Infectious Diseases|July 25, 2024
Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 InfectionZahra R Tehrani, Parham Habibzadeh, Robin Flinko, et al.
International Journal of Molecular Sciences|March 8, 2019
HDAC Inhibitors Induce <i>BDNF</i> Expression and Promote Neurite Outgrowth in Human Neural Progenitor Cells-Derived NeuronsAmir Bagheri, Parham Habibzadeh, Seyedeh Fatemeh Razavipour, et al.
BMC Medical Genetics|January 16, 2019
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case reportFateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, et al.
Frontiers in Neurology|September 26, 2019
A Novel <i>TTC19</i> Mutation in a Patient With Neurological, Psychological, and Gastrointestinal ImpairmentParham Habibzadeh, Soroor Inaloo, Mohammad Silawi, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Journal of Genetics|September 2, 2021
Investigating the association between common <i>DRD2/ANKK1</i> genetic polymorphisms and schizophrenia: a meta-analysisParham Habibzadeh, Azim Nemati, Hassan Dastsooz, et al.
BMC Medical Genetics|March 23, 2019
An immunocompetent patient with a nonsense mutation in NHEJ1 geneHossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, et al.
Biochemia Medica|August 11, 2020
Rate of re-positive RT-PCR test among patients recovered from COVID-19Parham Habibzadeh, Mohammad M Sajadi, Amir Emami, et al.
Cell Journal|November 27, 2021
Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in <i>DPAGT1</i> GeneZahra Tabatabaei, K Hadijeh Karbalaie, Parham Habibzadeh, et al.
BMC Gastroenterology|May 10, 2020
Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal EncephalomyopathyParham Habibzadeh, Mohammad Silawi, Hassan Dastsooz, et al.
BMC Medical Genetics|October 31, 2019
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case seriesGhazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, et al.
The Journal of Infectious Diseases|July 25, 2024
Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 InfectionZahra R Tehrani, Parham Habibzadeh, Robin Flinko, et al.
International Journal of Molecular Sciences|March 8, 2019
HDAC Inhibitors Induce <i>BDNF</i> Expression and Promote Neurite Outgrowth in Human Neural Progenitor Cells-Derived NeuronsAmir Bagheri, Parham Habibzadeh, Seyedeh Fatemeh Razavipour, et al.
BMC Medical Genetics|January 16, 2019
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case reportFateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, et al.
Frontiers in Neurology|September 26, 2019
A Novel <i>TTC19</i> Mutation in a Patient With Neurological, Psychological, and Gastrointestinal ImpairmentParham Habibzadeh, Soroor Inaloo, Mohammad Silawi, et al.
Pageof 6