Zobrazeno 1 - 10
of 470
pro vyhledávání: '"Vahid ziaee"'
Autor:
Kosar Asna Ashari, Nima Parvaneh, Kayvan Mirnia, Mehri Ayati, Maryam Saeedi, Farhad Salehzadeh, Mohammad Shahrooei, Razieh Sangsari, Pejman Rohani, Vahid Ziaee
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-7 (2024)
Abstract Background Gain of function (GOF) mutations in NOD-like receptor family CARD-containing 4 protein (NLRC4) gene induce a wide spectrum of autoinflammatory phenotypes. Currently, we categorize them into four groups: familial cold autoinflammat
Externí odkaz:
https://doaj.org/article/028afa411aba48dba285ddbd43f4f0f5
Autor:
Azadeh Zeinab Mirzaee, Setayesh Sadeghi, Reza Shiari, Vahid Ziaee, Amirhossein Karagah, Reza Sinaei, Shabnam Hajiani Ghotbabadi, Fatemeh Tahghighi, Mohammad Reza Fathi, Armin Shirvani, Aye Miremarati, Leila Ghasemi, Khosro Rahmani, Shahram Araghi, Vadood Javadi Parvaneh, Morteza Jaffaraghaei, Alireza Mohammadkarim
Publikováno v:
Biomedical and Biotechnology Research Journal, Vol 8, Iss 3, Pp 363-368 (2024)
Background: Systemic juvenile idiopathic arthritis (sJIA) is marked with arthritis and several features of systemic inflammation, including fever, rashes, hepatosplenomegaly, lymphadenopathy, and serositis. Interleukin-1 receptor blockers have been u
Externí odkaz:
https://doaj.org/article/08e68a9b3eb74ff8bf14222766789304
Autor:
Zahra Amirsardari, Fatemeh Amirsardari, Erfan Kohansal, Amir Ghaffari Jolfay, Maziar Gholampour Dehaki, Vahid Ziaee
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Background Kawasaki Disease (KD) involves arterial inflammation, primarily affecting the coronary arteries and leading to coronary artery lesions. Recent advancements in understanding the immunomodulatory roles of vitamin D have prompted inv
Externí odkaz:
https://doaj.org/article/749ae1eef74e49e3a6968c24e9d9ea33
Publikováno v:
Case Reports in Clinical Practice, Vol 8, Iss 5 (2024)
Pompe disease or type 2 glycogen storage disease (GSD), is an autosomal recessive disorder, occurs by deficiency of an enzyme (acid maltase) which degrades glycogen in lysosomes. It is classified into infantile and late onset types.Identifying PD pre
Externí odkaz:
https://doaj.org/article/f94baf9461f74b81bdd5eb95f0886f50
Publikováno v:
Reviews in Clinical Medicine, Vol 10, Iss 3, Pp 25-29 (2023)
Introduction: The symptoms and laboratory findings of Kawasaki disease (KD) and systemic-onset juvenile idiopathic arthritis (SoJIA) may overlap in the early phases. Coronary artery lesions are common complications seen in KD.Cases Presentation: In t
Externí odkaz:
https://doaj.org/article/d85d30b7328b408bbbefe7564e7f9713
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-9 (2023)
Abstract Background Wolman disease is a rare disease caused by the absence of functional liposomal acid lipase due to mutations in LIPA gene. It presents with organomegaly, malabsorption, and adrenal calcifications. The presentations can resemble hem
Externí odkaz:
https://doaj.org/article/916f641ff2894e8ba3e5076bbb1275aa
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-9 (2023)
Abstract Background Studies on Multisystem Inflammatory Syndrome in Children (MIS-C) and Kawasaki Disease (KD) have yielded inconsistent results and are lacking in Asian and African countries. This study aimed to compare the laboratory and clinical f
Externí odkaz:
https://doaj.org/article/0b09d817db054974bdfecf8af72eded2
Autor:
Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, Raheleh Assari, Morteza Heidari, Mohammadreza Fathi, Fatemeh Tahghighi Sharabian, Alireza Ronagh, Mohammad Shahrooei, Alireza Moafi, Nima Rezaei, Vahid Ziaee
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disease caused by mutations in the ADA2 gene. DADA2 has a broad spectrum of clinical presentations. Apart from systemic manifestations, we can
Externí odkaz:
https://doaj.org/article/4049764426fb404f90cf42653a6acc8d
Autor:
Elmira Hajiesmaeil Memar, Fatemeh Tahghighi, Sedigheh Yousefzadegan, Parisa Sadeghirad, Ashraf Mousavi, Ramin Zare Mahmoudabadi, Hossein Saeidi, Mehri Ayati, Sahar Naderi, Sara Memarian, Seyedmusa Zeinalabedin, Bahar Ashjaei, Hojatollah Raji, Leila Tahernia, Hosein Alimadadi, Vahid Ziaee
Publikováno v:
Case Reports in Surgery, Vol 2024 (2024)
Background. On December 2019, a novel coronavirus disease (COVID-19) spread worldwide and became a pandemic. Multisystem inflammatory syndrome in children (MIS-C) due to cytokine release syndrome following COVID-19 presents with various manifestation
Externí odkaz:
https://doaj.org/article/55f262ef11bb4c7f9a76f6a23e27c423
Autor:
Payman Sadeghi, Mojtaba Gorji, Raheleh Assari, Fatemeh Tahghighi, Seyed Reza Raeeskarami, Vahid Ziaee
Publikováno v:
Intensive Care Medicine Experimental, Vol 10, Iss 1, Pp 1-12 (2022)
Abstract Background Hyper-inflammatory syndrome in children and young adult occur 2–6 weeks after COVID-19 infection or closed contact with COVID-19 persons. In this study, the laboratory data and echocardiography and abdominal ultrasonography asse
Externí odkaz:
https://doaj.org/article/1faf4102e34d4f29a26f0cc3de896028