Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Azadeh Hoseini"'
Autor:
Marjaneh Zarkesh, Sadroddin Mahdipour, Safoora Aghili, Atefeh Jafari, Seyyedeh Azadeh Hoseini Nouri, Afagh Hassanzadeh Rad, Maryam Ghalandari, Manijeh Tabrizi
Publikováno v:
PLoS ONE, Vol 18, Iss 12 (2023)
Externí odkaz:
https://doaj.org/article/94857fe7dd044d0eabb07887d54cc1eb
Autor:
Shahin Koohmanaee, Seyyedeh Azadeh Hoseini Nouri, Vahid Aminzadeh, Manijeh Tabrizi, Reza Bayat, Fatemeh Kharaee, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Saber Najafi Chakoosari, Setila Dalili, Ehsan Kazemnejad Leili
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 9, Iss 1 (2023)
Background: Neuronal ceroid lipofuscinoses (NCL) is a rare progressive neurodegenerative disorder caused by more than 530 mutations of at least 13 different genes (CLN 1-14). NCL is a part of the lysosomal disease characterized by the presence of
Externí odkaz:
https://doaj.org/article/cfd2a7a53c8f4319be8462368a1ee2f9
Autor:
Shahin Koohmanaee, Amirhossein Tamimi, Soroush Ahmadimacciani, Atena Tamimi, Vahid Aminzadeh, Marjaneh Zarkesh, Seyyedeh Azadeh Hoseini Nouri, Fatemeh Rajaeipoor, Manijeh Tabrizi, Setila Dalili
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 7, Iss 4, Pp 236-243 (2021)
Background: Gonadal dysgenesis, the most common cause of primary amenorrhea, is characterized by absent or underdeveloped ovaries. Although the coexistence of gonadal dysgenesis and Mayer-Rokitansky-Küster-Hauser (MRKH) has been reported, it is stil
Externí odkaz:
https://doaj.org/article/19c98e37393143cd851b981b389bcd95
Akademický článek
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Autor:
Koohmanaee, Shahin1, Nouri, Seyyedeh Azadeh Hoseini1, Aminzadeh, Vahid1, Tabrizi, Manijeh1, Bayat, Reza1, Kharaee, Fatemeh1, Shahrokhi, Maryam2, Rad, Afagh Hassanzadeh1, Chakoosari, Saber Najafi3, Dalili, Setila1 setiladalili1346@yahoo.com, Leili, Ehsan Kazemnejad1
Publikováno v:
Caspian Journal of Neurological Sciences. Winter2023, Vol. 9 Issue 1, p50-55. 6p.
Autor:
Nioosha Mostofinezhad, Saeed Reza Ghaffari, Zeinab Barati, Laya Fakhri, Fatemeh Hoseininasab, Faezeh Mohamadhashem, Azadeh Hoseini, Amir Hosein Mahmoudi, Somayeh Darzi Ramandi, Koosha Jalilian, Maryam Rafati, Hosna Amiri
Publikováno v:
Ophthalmic Genetics. 43:262-267
BACKGROUND Next-generation sequencing has been proven to be a reliable method for the detection of genetic causes in heterogeneous ocular disorders. In this report an NGS-based diagnostic approach was taken to uncover the genetic etiology in a patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2d57fb2c292793b7d4c075697aec4c
https://doi.org/10.1080/13816810.2021.2002915
https://doi.org/10.1080/13816810.2021.2002915
Autor:
Marjaneh Zarkesh, Seyyedeh Azadeh Hoseini Nouri, Shahin Koohmanaee, Amirhossein Tamimi, Manijeh Tabrizi, Vahid Aminzadeh, Soroush Ahmadimacciani, Setila Dalili, Fatemeh Rajaeipoor, Atena Tamimi
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 7, Iss 4, Pp 236-243 (2021)
Background: Gonadal dysgenesis, the most common cause of primary amenorrhea, is characterized by absent or underdeveloped ovaries. Although the coexistence of gonadal dysgenesis and Mayer-Rokitansky-Küster-Hauser (MRKH) has been reported, it is stil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a58860a7682036e92d5dae1a3ef895
https://doi.org/10.32598/cjns.7.27.3
https://doi.org/10.32598/cjns.7.27.3
Autor:
Saeed R. Ghaffari, Maryam Rafati, Mahdi Shadnoush, Shokooh Pourbabaee, Mohammad Aghighi, Siamak Mirab Samiee, Jamshid Kermanchi, Mohammad R. Alaei, Shadab Salehpour, Davoud Amirkashani, Aria Setoodeh, Peymaneh Sarkhail, Reza Shervin Badv, Majid Aminzadeh, Siamak Shiva, Peyman Eshraghi, Hossein Moravej, Mahin Hashemipour, Noushin Rostampour, َAmir Ali Hamidieh, Bibi Shahin Shamsian, Sedigheh Shams, Daniel Zamanfar, Ayoub Ebrahimi, Ali Otadi, Seyedeh Zahra Tara, Zeinab Barati, Laya Fakhri, Azadeh Hoseini, Hosna Amiri, Somayeh Ramandi, Niusha Mostofinezhad, Zahra Pahlevani Kani, Elham Mohammadyari, Mahsa Khosravi, Masoome Saadati, Fatemeh Hoseininasab, Hamid Reza Khorram Khorshid, Younes Modaberisaber
Publikováno v:
Human mutationREFERENCES. 43(4)
Mucopolysaccharidoses (MPSs) are rare, heterogeneous inborn errors of metabolism (IEM) diagnosed through a combination of clinical, biochemical, and genetic investigations. The aim of this study was molecular characterization of the largest cohort of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0435c10f3a5e98cc74a094eba486a8f6
https://pubmed.ncbi.nlm.nih.gov/35005816
https://pubmed.ncbi.nlm.nih.gov/35005816
Autor:
Maryam, Rafati, Faezeh, Mohamadhashem, Koosha, Jalilian, Fatemeh, Hoseininasab, Laya, Fakhri, Azadeh, Hoseini, Hosna, Amiri, Zeinab, Barati, Somayeh, Darzi Ramandi, Nioosha, Mostofinezhad, Amir Hosein, Mahmoudi, Saeed Reza, Ghaffari
Publikováno v:
Ophthalmic genetics. 43(2)
Next-generation sequencing has been proven to be a reliable method for the detection of genetic causes in heterogeneous ocular disorders. In this report an NGS-based diagnostic approach was taken to uncover the genetic etiology in a patient with colo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1848d75f0961dd0c272abef6047ad21a
https://pubmed.ncbi.nlm.nih.gov/34791963
https://pubmed.ncbi.nlm.nih.gov/34791963
Autor:
Sara Khorami Sarvestani, Azadeh Hoseini, Koosha Jalilian, Azadeh Soltani, Maryam Rafati, Saeed Reza Ghaffari, Haleh Soltanghoraee
Publikováno v:
Avicenna Journal of Medical Biotechnology
Background: Around 70% of all pregnancies (Including 15% of clinically-recognized ones) are lost due to various fetal or maternal disorders. Chromosomal aneuploidies are among the most common causes of pregnancy loss. Standard chromosome analysis usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2954e57d8932c5d4f36d59338084674a
https://pubmed.ncbi.nlm.nih.gov/34484644
https://pubmed.ncbi.nlm.nih.gov/34484644