Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hassan Birjandi"'
Publikováno v:
Iranian Journal of Neonatology, Vol 13, Iss 4, Pp 17-20 (2022)
Background: The prenatal diagnosis of coarctation of aorta (CoA) remains a major challenge, as the false-positive diagnosis is fairly common. The purpose of this study was to find some useful prenatal sonographic markers compatible with the postnatal
Externí odkaz:
https://doaj.org/article/9152fd39a29144f58988aded9763fc45
Publikováno v:
Iranian Journal of Neonatology, Vol 10, Iss 1, Pp 86-88 (2019)
Background: Vein of Galen aneurysm (VGA) is the most common form of symptomatic cerebrovascular malformation in neonates. It develops in a fetus in the first trimester of pregnancy due to unknown reasons, but it is likely to have a genetic etiology.
Externí odkaz:
https://doaj.org/article/e85265577c944098ad9b1281668eabd1
Autor:
Reza Saeidi, Ashraf Mohammadzadeh, Ahmadshah Farhat, Mohammadreza Naghibi, Hassan Birjandi, Saeedreza Lotfi
Publikováno v:
Iranian Journal of Neonatology, Vol 8, Iss 3, Pp 78-81 (2017)
Background: One-third of all major congenital anomalies are Congenital heart disease (CHD) and Reported CHD prevalence increased over time and in Asian countries is more than western countries. Ectopia cordis (EC) is a rare congenital anomaly with an
Externí odkaz:
https://doaj.org/article/7d159f4f95004ca88427cd66e9dfad0e
Autor:
Hassan Mottaghi Moghaddam Shahri, Hojjat Mortezaeian, Ata Firouzi, Zahra Khajali, Hassan Birjandi, Mohammad Hassan Nezafati, Hassan Radmehr, Keyhan Sayadpour Zanjani
Publikováno v:
Annals of Vascular Surgery. 85:292-298
Coarctation of the aorta is a common cardiac disease in Turner syndrome. Evidence indicates that surgery and balloon angioplasty in infants and small children do not have any added risk of mortality or complication in these patients. Stenting in olde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf32f77c6becf83d88c11a7a365de04
https://doi.org/10.1016/j.avsg.2022.02.020
https://doi.org/10.1016/j.avsg.2022.02.020
Autor:
Constance Maurer, Olga Boleti, Paria Najarzadeh Torbati, Farzaneh Norouzi, Anna Nicole Rebekah Fowler, Shima Minaee, Khalid Hama Salih, Mehdi Taherpour, Hassan Birjandi, Behzad Alizadeh, Aso Faeq Salih, Moniba Bijari, Henry Houlden, Alan Michael Pittman, Reza Maroofian, Yahya H. Almashham, Ehsan Ghayoor Karimiani, Juan Pablo Kaski, Eissa Ali Faqeih, Farveh Vakilian, Yalda Jamshidi
Publikováno v:
Genes; Volume 14; Issue 1; Pages: 182
Inherited cardiomyopathies are a prevalent cause of heart failure and sudden cardiac death. Both hypertrophic (HCM) and dilated cardiomyopathy (DCM) are genetically heterogeneous and typically present with an autosomal dominant mode of transmission.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68a9afd3562cffde2ecd4e4aca21854
Autor:
Tamara T. Koopmann, Yalda Jamshidi, Mohammad Naghibi-Sistani, Heleen M. van der Klift, Hassan Birjandi, Zuhair Al-Hassnan, Abdullah Alwadai, Giovanni Zifarelli, Ehsan G. Karimiani, Sahar Sedighzadeh, Amir Bahreini, Nayereh Nouri, Merlene Peter, Kyoko Watanabe, Hermine A. van Duyvenvoorde, Claudia A. L. Ruivenkamp, Aalbertine K. K. Teunissen, Arend D. J. Ten Harkel, Sjoerd G. van Duinen, Monique C. Haak, Carlos E. Prada, Gijs W. E. Santen, Reza Maroofian
Publikováno v:
European Journal of Human Genetics, 31, 97-104. SPRINGERNATURE
Autosomal dominant variants in LDB3 (also known as ZASP), encoding the PDZ-LIM domain-binding factor, have been linked to a late onset phenotype of cardiomyopathy and myofibrillar myopathy in humans. However, despite knockout mice displaying a much m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af3fd1cb260d1f202ffaee8cd0bfa728
https://pubmed.ncbi.nlm.nih.gov/36253531
https://pubmed.ncbi.nlm.nih.gov/36253531
Autor:
Behzad Alizadeh, Hassan Mottaghi, Yalda Ravanshad, Fatemeh Tara, Shirin Sadat Ghiasi, Mohammadreza Naghibi, Hassan Birjandi, Elahe Heidari
Publikováno v:
Electronic Physician. 12:7668-7673
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bcc17aa67cc31577d8c0c6996d01712
https://doi.org/10.19082/7668
https://doi.org/10.19082/7668