Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Gilani, Abolfazl"'
Autor:
Hakimzadeh, Zahra1 (AUTHOR), Gilani, Abolfazl2 (AUTHOR), Yousefichaijan, Parsa3 (AUTHOR), Sarmadian, Roham4 (AUTHOR) rsarmadian@yahoo.com
Publikováno v:
Journal of Medical Case Reports. 2/24/2024, Vol. 18 Issue 1, p1-5. 5p.
Autor:
Salajegheh, Pouria1 (AUTHOR), Gilani, Abolfazl2 (AUTHOR), Yazdi, Farzaneh3 (AUTHOR), Sarmadian, Roham4 (AUTHOR), Habibzadeh, Adrina5,6 (AUTHOR) adrina.hbz77@gmail.com
Publikováno v:
Clinical Case Reports. Oct2023, Vol. 11 Issue 10, p1-4. 4p.
Autor:
Hojabri, Mahsa1 (AUTHOR), Gilani, Abolfazl2 (AUTHOR), Irilouzadian, Rana3 (AUTHOR), Nejad biglari, Habibe4 (AUTHOR), Sarmadian, Roham5 (AUTHOR) rsarmadian@yahoo.com
Publikováno v:
Clinical Medicine Insights: Case Reports. 7/18/2023, p1-8. 8p.
Autor:
Gilani, Abolfazl1 (AUTHOR), Sarmadian, Roham2 (AUTHOR) rsarmadian@yahoo.com, Kahbazi, Manijeh2 (AUTHOR), Yousefichaijan, Parsa3 (AUTHOR)
Publikováno v:
BMC Infectious Diseases. 12/28/2022, p1-4. 4p.
Autor:
Gilani, Abolfazl1, Khaniki, Saeedeh Hajebi2, Fard, Fatemeh Khazaei3, Sirjani, Ehsan Baradaran4, Sarmadian, Roham5 rsarmadian@yahoo.com
Publikováno v:
Vaccine Research. 2022, Vol. 9 Issue 2, p42-46. 5p.
Autor:
Sarmadian, Roham1 (AUTHOR), Gilani, Abolfazl2 (AUTHOR) Abol.gilani95@gmail.com, Biglari, Habibe Nejad3 (AUTHOR)
Publikováno v:
Oxford Medical Case Reports. Mar2023, Vol. 2023 Issue 3, p1-3. 3p.
Autor:
Hojabri, Mahsa, Gilani, Abolfazl, Irilouzadian, Rana, Nejad biglari, Habibe, Sarmadian, Roham
Supplemental material, sj-docx-1-icr-10.1177_11795476231188061 for Adolescence Onset Primary Coenzyme Q10 Deficiency With Rare CoQ8A Gene Mutation: A Case Report and Review of Literature by Mahsa Hojabri, Abolfazl Gilani, Rana Irilouzadian, Habibe Ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::770c212f5d1a28032f71bcbd04e8020b
Autor:
Ghoshouni, Hamed, Sarmadian, Roham, Irilouzadian, Rana, Biglari, Habibe Nejad, Gilani, Abolfazl
Supplemental material, sj-docx-1-hic-10.1177_23247096231168109 for A Rare Case of Cerebrotendinous Xanthomatosis Associated With a Mutation on COG8 Gene by Hamed Ghoshouni, Roham Sarmadian, Rana Irilouzadian, Habibe Nejad Biglari and Abolfazl Gilani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753ee0668ce91f899180ae4d6b9a2fe5
Autor:
Ghasemikhah, Reza, Hakimzadeh, Zahra, Gilani, Abolfazl, Sarmadian, Hossein, Sarmadian, Roham, Yousefbeigi, Negin
Publikováno v:
Clinical Case Reports; Jul2023, Vol. 11 Issue 7, p1-5, 5p
Autor:
Ghoshouni, Hamed, Sarmadian, Roham, Irilouzadian, Rana, Biglari, Habibe Nejad, Gilani, Abolfazl
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports; 4/21/2023, p1-4, 4p