Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kimia Najafi"'
Autor:
Amirmohammad Khalaji, Amir Hossein Behnoush, Yeganeh Pasebani, Ali Rafati, Tara Mahmoodi, Alireza Arzhangzadeh, Sima Shamshiri Khamene, Izat MohammadKhawajah, Mehdi Mehrani, Ali Vasheghani-Farahani, Farzad Masoudkabir, Kimia Najafi, Mani K. Askari, Anil Harrison, John R. Nelson, Kaveh Hosseini, Adrian V. Hernandez
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Triglyceride-glucose index (TyG), a surrogate marker of insulin resistance (IR), could be a potential prognostic marker in patients with acute coronary syndromes (ACS). We evaluated the effect of the TyG index on major adverse car
Externí odkaz:
https://doaj.org/article/a99532fca45f4e6ab99d78058c8184de
Autor:
Kaveh Hosseini, Amirmohammad Khalaji, Amir Hossein Behnoush, Hamidreza Soleimani, Saghar Mehrban, Zahra Amirsardari, Kimia Najafi, Mehrshad Fathian Sabet, Negin Sadat Hosseini Mohammadi, Shayan Shojaei, Farzad Masoudkabir, Hassan Aghajani, Mehdi Mehrani, Hadie Razjouyan, Adrian V. Hernandez
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Metabolic syndrome (MetS) poses an additional risk for the development of coronary artery disease and major adverse cardiac and cerebrovascular events (MACCE). In this study, we investigated the association between MetS and its components an
Externí odkaz:
https://doaj.org/article/1f500c2ca9894da98037fd694be06ef3
Autor:
Kaveh Hosseini, Hamidreza Soleimani, Kiarash Tavakoli, Milad Maghsoudi, Narges Heydari, Yasmin Farahvash, Ali Etemadi, Kimia Najafi, Mani K Askari, Rahul Gupta, Diaa Hakim, Kazem Rahimi
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0307120 (2024)
AimSleep duration has been suggested to be associated with hypertension (HTN). However, evidence of the nature of the relationship and its direction has been inconsistent. Therefore, we performed a meta-analysis to assess the relationship between sle
Externí odkaz:
https://doaj.org/article/d88bda7bae974574a33461e0bdd02bfa
Autor:
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Recurrent miscarriages occur in about 5% of couples trying to conceive. In the past decade, the products of miscarriage have been studied using array comparative genomic hybridization (a-CGH). Within the last decade, an association has been
Externí odkaz:
https://doaj.org/article/dfd9e1bd65df4bc1a6c09534993ad5b0
Autor:
Maryam Taghdiri, Atie Kashef, Golemaryam Abbassi, Azadeh Moshtagh, Neda Sadatian, Majid Fardaei, Kimia Najafi, Roxana Kariminejad
Publikováno v:
Clinical Case Reports, Vol 7, Iss 6, Pp 1149-1153 (2019)
Key Clinical Message Different mutations in glutamate receptor ionotropic delta 2 (GRID2) gene cause cerebellar ataxia in human. We report the largest homozygous deletion of the GRID2 gene reported to date, most probably causing complete loss of the
Externí odkaz:
https://doaj.org/article/43618e758e3d42cb93b887e02caf4695
Autor:
Kimia Najafi, Soheila Gholami, Azadeh Moshtagh, Masood Bazrgar, Neda Sadatian, Golemaryam Abbasi, Parvin Rostami, Soheila Khalili, Mojgan Babanejad, Bahareh Nourmohammadi, Negin Faramarzi Garous, Hossein Najmabadi, Roxana Kariminejad
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background Pregnancy loss affects 10%–15% of pregnancies and is caused by several factors, maternal and fetal. Most common cause is chromosomal aneuploidy and has traditionally been detected by karyotyping product of conception and/or feta
Externí odkaz:
https://doaj.org/article/ab057e8a446d4424b39cf48405a5896b
Autor:
Kimia Najafi, Roxana Kariminejad, Kaveh Hosseini, Azadeh Moshtagh, Gole Maryam Abbassi, Neda Sadatian, Masood Bazrgar, Ariana Kariminejad, Mohamad Hassan Kariminejad
Publikováno v:
Case Reports in Genetics, Vol 2017 (2017)
Introduction. Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive hypomyelinating leukodystrophy characterized by nystagmus, spastic quadriplegia, ataxia, and developmental delay. It is caused by mutation in the PLP1 gene. Case Description. W
Externí odkaz:
https://doaj.org/article/2754fb432cfb4b61bc9d493154964087
Autor:
Ariana Kariminejad, Siavash Ghaderi‐Sohi, Soheila Gholami, Kimia Najafi, Roxana Kariminejad, Raoul C. M. Hennekam
Publikováno v:
American journal of medical genetics. Part A, 191(2), 370-377. Wiley-Liss Inc.
The 5p13 microduplication syndrome is a contiguous gene syndrome characterized by developmental delay intellectual disability, hypotonia, unusual facies with marked variability, mild limb anomalies, and in some cases brain malformations. The duplicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8c974fa9377f260fb8cf5413891bc7
https://pure.amc.nl/en/publications/5p13-microduplication-in-a-malformed-fetus-and-his-unaffected-father(f9a4bc9c-790a-41c9-9c1b-878be48d5cff).html
https://pure.amc.nl/en/publications/5p13-microduplication-in-a-malformed-fetus-and-his-unaffected-father(f9a4bc9c-790a-41c9-9c1b-878be48d5cff).html
Autor:
Atie Kashef, Azadeh Moshtagh, Majid Fardaei, Roxana Kariminejad, Neda Sadatian, Kimia Najafi, Golemaryam Abbassi, Maryam Taghdiri
Publikováno v:
Clinical Case Reports, Vol 7, Iss 6, Pp 1149-1153 (2019)
Clinical Case Reports
Clinical Case Reports
Key Clinical Message Different mutations in glutamate receptor ionotropic delta 2 (GRID2) gene cause cerebellar ataxia in human. We report the largest homozygous deletion of the GRID2 gene reported to date, most probably causing complete loss of the
Autor:
Ariana Kariminejad, Kimia Najafi, Roxana Kariminejad, Hossein Najmabadi, Siavash Ghaderi-Sohi, Zohreh Mehrjoo, Fariba Ardalani
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Recurrent miscarriages occur in about 5% of couples trying to conceive. In the past decade, the products of miscarriage have been studied using array comparative genomic hybridization (a-CGH). Within the last decade, an association has been proposed