Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Shahin Abdollahi Fakhim"'
Publikováno v:
مجله پزشکی دانشگاه علوم پزشکی تبریز, Vol 43, Iss 1, Pp 160-166 (2021)
Background: Cleft lip and palate are the most common congenital malformations of the head and neck. These disorders have high economic cost for families and impose a heavy psychological burden on children. Performing early primary reconstructive surg
Externí odkaz:
https://doaj.org/article/b5ba652c952f440f809c6294fe4f91cb
Publikováno v:
مجله پزشکی دانشگاه علوم پزشکی تبریز, Vol 42, Iss 6, Pp 684-691 (2021)
Background: Sleep-disordered breathing is a common problem in children and is associated with increased cardiovascular morbidity. The circulating level of C-reactive protein, a pro-inflammatory protein, is associated with increased risk for atheroscl
Externí odkaz:
https://doaj.org/article/7d96c0d906384074beae3e21a7669ee2
Autor:
Maghsood Shakeer, Amir Mehdizadeh, Rana Ezzeddini, Babollah Ghasemi, Yalda Jabbari Moghaddam, Shahin Abdollahi Fakhim, Masoud Saleh Moghaddam, Masoud Darabi
Publikováno v:
The Journal of Qazvin University of Medical Sciences, Vol 22, Iss 4, Pp 4-12 (2018)
Background: Inflammatory and obstructive tonsillar diseases are among the most common diseases in childhood, and tonsillectomy is one of the most common surgical procedures in children. Current evidence indicates the potential association between cho
Externí odkaz:
https://doaj.org/article/224bab9a89b44ac2be01ce2da8debc16
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 28, Iss 2, Pp 135-139 (2016)
Introduction: Orofacial clefts are among the most common congenital anomalies. Patients presenting with orofacial clefts often require surgery or other complex procedures. A cleft lip or palate can be a single anomaly or a part of multiple congenital
Externí odkaz:
https://doaj.org/article/391faabc1ee44221923e3e01e67081f6
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 26, Iss 4, Pp 263-266 (2014)
Introduction: First branchial cleft anomalies manifest with duplication of the external auditory canal. Case Report: This report features a rare case of microtia and congenital middle ear and canal cholesteatoma with first branchial fistula. External
Externí odkaz:
https://doaj.org/article/041c86773c2d4727811772d6bc87187f
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 25, Iss 73, Pp 259-262 (2013)
Introduction: Tessier facial cleft is among the rarest facial clefts reported in literatures and there are many issues arguing about its multidisciplinary repairing techniques. Tessier number 4 and 5 are extremely rare facial anomalies. There are few
Externí odkaz:
https://doaj.org/article/5a3e70c9a56245a79f875d0dbf7c9f7b
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 24, Iss 66, Pp 45-50 (2012)
Introduction: Nager syndrome is a malformation resulting from problems in the development of the first and second branchial arches and limb buds. The cause of the abnormal development of the pharyngeal arches in Nager syndrome is unknown. It is also
Externí odkaz:
https://doaj.org/article/881d4a3187364687bcf5eed367f1c2f2
Autor:
Lida Jabbari Gharehgheshlaghi, Yalda Yazdani, Zahra Hasanpour Segherlou, Shahin Abdollahi Fakhim, Masoud Nouri-Vaskeh
Background: Different timelines are preferred for repair surgeries in patients with unilateral complete cleft lip and palate (UCLP). The aim of this study was to evaluate the effects of early palatoplasty on procedural related blood loss (anemia) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3aacf4c349d5c5febb04f0945dd448d
https://doi.org/10.21203/rs.3.rs-1325620/v1
https://doi.org/10.21203/rs.3.rs-1325620/v1
Publikováno v:
The Cleft Palate-Craniofacial Journal. 58:1281-1286
Objective: Orofacial clefts (OFCs) can occur as an isolated defect or as a manifestation of other syndromes. The current study aimed to evaluate demographic characteristics and distribution of different types of accompanying anomalies for OFCs in the
Publikováno v:
Journal of stomatology, oral and maxillofacial surgery. 123(1)
This study aimed to compare the developmental characteristics of bony nasopharyngeal (NP) in children with cleft palate (CP) and non-cleft subjects.This study was conducted on 64 non-syndromic CP patients who underwent repair surgery and 23 non-cleft