Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Houman Alizadeh"'
Autor:
Morteza Zarrabi, Masood Ghahvechi Akbari, Man Amanat, Anahita Majmaa, Ali Reza Moaiedi, Hadi Montazerlotfelahi, Masoumeh Nouri, Amir Ali Hamidieh, Reza Shervin Badv, Hossein Karimi, Ali Rabbani, Ali Mohebbi, Shahram Rahimi-Dehgolan, Rosa Rahimi, Ensieh Dehghan, Massoud Vosough, Saeed Abroun, Farhad Mahvelati Shamsabadi, Ali Reza Tavasoli, Houman Alizadeh, Neda Pak, Gholam Reza Zamani, Mahmoud Mohammadi, Mohsen Javadzadeh, Mohammad Ghofrani, Seyed Hossein Hassanpour, Morteza Heidari, Mohammad Mehdi Taghdiri, Mohamad Javad Mohseni, Zahra Noparast, Safdar Masoomi, Mehrdad Goudarzi, Masood Mohamadpour, Razieh Shodjaee, Solaleh Samimi, Monireh Mohammad, Mona Gholami, Nahid Vafaei, Leyli Koochakzadeh, Amir Valizadeh, Reza Azizi Malamiri, Mahmoud Reza Ashrafi
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Introduction The current multi-center, randomized, double-blind study was conducted among children with cerebral palsy (CP) to assess the safety and efficacy of umbilical cord blood mononuclear cell (UCB-MNC). We performed the diffusion tens
Externí odkaz:
https://doaj.org/article/6f139e136d1f4fa284713638f9f33fef
Publikováno v:
African Journal of Paediatric Surgery, Vol 19, Iss 1, Pp 13-17 (2022)
Introduction: Appendicitis is one of the most common paediatric surgical emergencies occurring in about 7% of healthy children. To make a definitive diagnosis preferably avoiding unnecessary X-ray radiation exposure, ultrasound is the ideal modality.
Externí odkaz:
https://doaj.org/article/232b081133ee4de199460187acb558ae
Autor:
Reyhaneh Kameli, Man Amanat, Zahra Rezaei, Sareh Hosseionpour, Sedigheh Nikbakht, Houman Alizadeh, Mahmoud Reza Ashrafi, Abdolmajid Omrani, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six. Defective RNASET2 leads to RNASET2-deficien
Externí odkaz:
https://doaj.org/article/da85c8a47676435d916fcf8992d52ec5
Autor:
Parviz Tabatabaie, Asghar Aghamohammadi, Setareh Mamishi, Anna Isaeian, Golnaz Heidari, Sina Abdollahzade, Pirouz Pirouzi, Nima Rezaei, Hassan Heidarnazhad, Bahram MirSaeid Ghazi, Mehdi Yeganeh, Taher Cheraghi, Hasan Abolhasani, Shiva Saghafi, Houman Alizadeh, Mohammad Reza Anaraki
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 7, Iss 2 (2008)
Bronchiectasis is a chronic debilitating condition characterized by abnormal dilated thick-walled bronchi. To investigate humoral immune function in bronchiectatic patients, this study was performed. Forty patients with established diagnosis of bronc
Externí odkaz:
https://doaj.org/article/05f15c3b403e496885eb4b239e5fcd51
Publikováno v:
Indian Journal of Otolaryngology and Head & Neck Surgery. 74:5806-5809
To assess the efficacy of intralesional injection of bleomycin for treatment of pediatric lymphangiomas in head and neck region in Iranian population. This prospective study was conducted from February 2017 to March 2019. All consecutive patients pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29fab49783bee63914cfc8ea3d7733b4
https://doi.org/10.1007/s12070-021-02411-4
https://doi.org/10.1007/s12070-021-02411-4
Publikováno v:
African Journal of Paediatric Surgery: AJPS
African Journal of Paediatric Surgery, Vol 19, Iss 1, Pp 13-17 (2022)
African Journal of Paediatric Surgery, Vol 19, Iss 1, Pp 13-17 (2022)
Introduction: Appendicitis is one of the most common paediatric surgical emergencies occurring in about 7% of healthy children. To make a definitive diagnosis preferably avoiding unnecessary X-ray radiation exposure, ultrasound is the ideal modality.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fff7e1e90d9d2dd0d4e95122e1d4d66
https://pubmed.ncbi.nlm.nih.gov/34916345
https://pubmed.ncbi.nlm.nih.gov/34916345
Autor:
Steven Cen, Amir Emami, Houman Alizadeh, Nazila Tayari, Fernando Fleischman, Leah Lin, Farhood Saremi
Publikováno v:
European Journal of Radiology. 89:60-66
Various degrees of aortic valve rotation may be seen in individuals with no history of congenital cardiovascular malformations, but its association with aortic sizes has not been studied.Gated computed tomographic (CT angiograms in 217 patients were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efcc3667bd23b11ecb2297deb2a535c6
https://doi.org/10.1016/j.ejrad.2017.01.009
https://doi.org/10.1016/j.ejrad.2017.01.009
Autor:
Sareh Hosseionpour, Mahmoud Reza Ashrafi, Masoud Garshasbi, Man Amanat, Reyhaneh Kameli, Abdolmajid Omrani, Sedigheh Nikbakht, Houman Alizadeh, Ali Reza Tavasoli, Zahra Rezaei
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Background Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six. Defective RNASET2 leads to RNASET2-deficient leukoen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da80e125e25432197d0b9fe0f5860bf
http://europepmc.org/articles/PMC6660666
http://europepmc.org/articles/PMC6660666
Autor:
Sareh Hosseinpour, Reyhaneh Kameli, Mohammad Barzegar, Shahram Sadeghvand, Houman Alizadeh, Nejat Mahdieh, Ali Reza Tavasoli, Mahmoud Reza Ashrafi, Zahra Rezaei
Publikováno v:
Iranian Journal of Pediatrics. 29
Megalencephalic leukoencephalopathy with subcortical cysts (MLC), a demyelination leukodystrophy, is usually characterized by early-onset macrocephaly and gradually progressive motor and mild mental deterioration. Variable clinical expression has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fe6f678e1872c1d36823337c8744a2c
https://doi.org/10.5812/ijp.91110
https://doi.org/10.5812/ijp.91110
Autor:
Sareh Hosseinpour, Houman Alizadeh, Nejat Mahdieh, Mahmoud Reza Ashrafi, Man Amanat, Masoud Mohammadpour, Ali Reza Tavasoli, Zahra Rezaei, Nahideh Khosroshahi
Publikováno v:
Neuropediatrics. 50(2)
Leukodystrophies are heterogeneous group of genetic white matter disorders with a wide range of neurologic and systemic manifestations. Defects in genes encoding aminoacyl tRNA (transfer ribonucleic acid) synthetase enzymes (aaRSs) are recently ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::641cf1685fbeb6402d01ab1245533705
https://pubmed.ncbi.nlm.nih.gov/30791064
https://pubmed.ncbi.nlm.nih.gov/30791064