Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Mahdkhah A"'
Autor:
Lotfinia, Iraj, Salehpoor, Firooz, Riazi, Ali, Aminmansoor, Bahram, Sourani, Arman, Mahdkhah, Ata
Publikováno v:
In Interdisciplinary Neurosurgery: Advanced Techniques and Case Management December 2023 34
Publikováno v:
In Interdisciplinary Neurosurgery: Advanced Techniques and Case Management December 2023 34
Publikováno v:
Interdisciplinary Neurosurgery, Vol 34, Iss , Pp 101840- (2023)
Introduction: Diastemamtomyelia is a rare congenital disorder, caused by longitudinal duplication of the spinal cord. Some patients are asymptomatic at birth, leading to delayed diagnosis. The average age of the patients at the time of diagnosis is 5
Externí odkaz:
https://doaj.org/article/e249ab2bdb824a3cbc11628dc50781a3
Publikováno v:
Interdisciplinary Neurosurgery, Vol 34, Iss , Pp 101809- (2023)
Introduction: Craniosynostosis is a congenital anomaly disturbing children’s cognitive disability and motor status and appearance. The present study aimed to determine the physical and neurocognitive outcomes of children with primary non-syndromic
Externí odkaz:
https://doaj.org/article/d132c37639f14017b1065dd62e745e8b
Autor:
Rezakhah, Amir, Kobets, Andrew J., Emami Sigaroudi, Faezeh, Mahdkhah, Ata, Barshan, Jalal, Gharajedaghi, Ali, Naseri Alavi, Seyed Ahmad
Publikováno v:
In World Neurosurgery July 2023 175:e1300-e1306
Publikováno v:
In Interdisciplinary Neurosurgery: Advanced Techniques and Case Management June 2023 32
Publikováno v:
Interdisciplinary Neurosurgery, Vol 33, Iss , Pp 101764- (2023)
Introduction: Pneumocephalus refers to the presence of air inside the cranial cavity. The presence of air in the cranial cavity without spinal involvement following penetrating trauma to the spine is a very rare condition. In this report, we present
Externí odkaz:
https://doaj.org/article/2f19445603574ae594b1c1bcf3ed2372
Publikováno v:
Interdisciplinary Neurosurgery, Vol 32, Iss , Pp 101757- (2023)
Background and objective: Craniosynostosis is the premature closure of one or more of the cranial sutures, which leads to skull deformities and other complications. Non-syndromic craniosynostosis (NSCS) usually involves only one cranial suture. Unico
Externí odkaz:
https://doaj.org/article/d24f857584d943c8b6d1a0cc684dec86
Autor:
Homayoun Tabesh, Ali Riazi, Mehdi Mahmoodkhani, Mohammad Sharafi, Arman Sourani, Ata Mahdkhah, Mina Foroughi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract A 6‐year‐old girl with persistent headaches and the visual problem was diagnosed as a delayed onset cranial pansynostosis with concurrent type 1.5 Arnold‐Chiari malformation. She underwent multi‐sutural reconstructive surgery and fol
Externí odkaz:
https://doaj.org/article/5c4977d8e74441c59711b432c3c26979
Autor:
Ata Mahdkhah, Firooz Salehpour, Iraj Lotfinia, Ali Riazi, Farhad Mirzaee, Saba Asghari Kaleibar
Publikováno v:
Interdisciplinary Neurosurgery, Vol 28, Iss , Pp 101471- (2022)
Alkaptonuria (AKU) is an uncommon disorder which is inherited as an autosomal recessive condition. Although intervertebral disc degeneration can be detected in the expected course of AKU, revealing of the disease by black disc color change in old pat
Externí odkaz:
https://doaj.org/article/fadfb0f28c8d4cd089a97cf3bb27a8c6