Zobrazeno 1 - 10
of 24
pro vyhledávání: '"leila Tahernia"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Necrotizing pneumonia (NP) is the destruction of the interstitial part of the lung due to severe infection. One cause of this rare and fatal condition in pediatrics is Acinetobacter. Severe infections, especially pneumonia, can p
Externí odkaz:
https://doaj.org/article/425ff86176494a5f82eef3a347635632
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:
Masoud Mohammadpour, Seyed Abbas Hassani, Meisam Sharifzadeh, Leila Tahernia, Setareh Mamishi, Bahareh Yaghmaie, Zeinab Najafi, Farzaneh Beirami, Mehrnoush Afsharipour, Maryam Minuyeefar, Mina Dolatzadeh, Neda Pak, Anahita Majmaa, Zahra Zamani, Shima Mahmoudi
Publikováno v:
International Journal of Clinical Practice, Vol 2022 (2022)
Introduction. In late February 2020, after we had informed about the presence of some cases of COVID-19 in Iran and its rapid spread throughout the country, we decided to make the necessary arrangements for patients with critical conditions in Pediat
Externí odkaz:
https://doaj.org/article/95f661c23a5e4fb29100e132281cfa7a
Autor:
Mohammad Vafaee‐Shahi, Saeide Ghasemi, Mehran Beiraghi Toosi, Mahmoud Reza Ashrafi, Reza Shervin Badv, Ali Reza Tavasoli, Leila Tahernia
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract We report a patient with complex clinical presentation including multiple neurological symptoms and eye involvement. Upon genetic investigation, the patient was found to carry a novel homozygous mutation in the NDUFS4 gene, thus adding to th
Externí odkaz:
https://doaj.org/article/58d33fd325714bb888c58f92bad9772c
Publikováno v:
Autoimmune Diseases, Vol 2017 (2017)
Background. Systemic lupus erythematosus (SLE) is a frequent rheumatology disorder among children. Since hepatic involvement is a common systemic manifestation in lupus, the frequency and type of hepatic involvement were determined in pediatric cases
Externí odkaz:
https://doaj.org/article/2274fa4ac9604bb0a98ca0c299fc5cec
Background: Herpes simplex virus type-2 could hardly lead to encephalitis in human-being. Some DNA viruses could be reactivated by COVID-19 infection such as HSV-1 and HSV-2 viruses. An uncommon presentation of HSV-2 was detected as cerebellitis in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c0f695b934a1d5f7a14b1091ce9bb6
https://doi.org/10.21203/rs.3.rs-2310381/v1
https://doi.org/10.21203/rs.3.rs-2310381/v1
Publikováno v:
The Open Public Health Journal. 15
Objective: To evaluate the role of ID in the pathogenesis of FS. Methods: In this case-control study (2014-2016), 70 children were studied, 35 children with FS and 35 (controls)children with febrile diseases without convulsion (The mean age of cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2617823be5ca0074d86953a4b8e744e7
https://doi.org/10.2174/18749445-v15-e2208102
https://doi.org/10.2174/18749445-v15-e2208102
Publikováno v:
Infectious Disorders - Drug Targets. 22
Background: A safe and effective rubella vaccine is available and prescribed in IRAN. Objective: This is a survey of CRS cases collected based on WHO criteria one decade after the MR vaccination campaign (2003) Methods: This Multi-stage prospective/c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::495b50bcf24909aebb4032a626e64a7e
https://doi.org/10.2174/1871526521666211213161712
https://doi.org/10.2174/1871526521666211213161712
Autor:
Masood Ghahvechi-Akbar, Reza Hajati, Davood Zare-Abdollahi, Afagh Alavi, Saeideh Ghasemi, Leila Tahernia, Mohammad Vafaee-Shahi, Atefeh Davarzani
Publikováno v:
Current Journal of Neurology
Background: Giant axonal neuropathy (GAN) is a very rare fatal neurodegenerative disorder with clinical and allelic heterogeneity. The disease is caused by mutations in the GAN (gigaxonin) gene. Herein, we reported the clinical presentations and resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25512049149c8fc68c28bd5be8c5f2cb
http://europepmc.org/articles/PMC8236428
http://europepmc.org/articles/PMC8236428
Publikováno v:
Clinical neurology and neurosurgery. 215
This is a case report of Methenyl Tetrahydrofolate synthetase deficiency (MTHFS deficiency) characterized by global developmental delay, cerebral hypomyelination, severe spastic tonicity in extremities, and microcephaly. Mutation in the MTHFS gene wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ec512bf0f77a32194a422097012c9c0
https://pubmed.ncbi.nlm.nih.gov/35219051
https://pubmed.ncbi.nlm.nih.gov/35219051