Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Asieh Mosallanejad"'
Autor:
Hedyeh Saneifard, Marjan Shakiba, Mohammadreza Alaei, Asieh Mosallanejad, Shirin Ghanefard, Mehrdad Yasaei, Kimia Karimi Toudeshki
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 40, Iss , Pp 101124- (2024)
Niemann Pick Type C disease is a rare and progressive neurodegenerative lysosomal storage disorder caused by autosomal recessive mutations in the NPC1 and NPC2 genes. It is characterized by the accumulation of multiple lipid species in the endolysoso
Externí odkaz:
https://doaj.org/article/d77ce205b35a4fb19f0cb8bf467c1076
Autor:
Marjan Shakiba, Mehrdad Yasaei, Hedyeh Saneifard, Asieh Mosallanejad, Mohammad Reza Alaei, Farzad Kobarfard, Marjan Esfahanizadeh, Narges Anousheh
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 40, Iss , Pp 101103- (2024)
Inherited metabolic diseases (IMD) are a group of rare genetic disorders that can present with a variety of symptoms. Since these disorders are hard to treat once the symptoms occur, neonatal screening may be a logical strategy. Here we evaluate the
Externí odkaz:
https://doaj.org/article/70bbb3f9e5b946568cd671c51e298f11
Autor:
Mohammad Sadegh Adel Mehraban, Asieh Mosallanejad, Mehdi Mohammadi, Ozra Tabatabaei Malazy, Bagher Larijani
Publikováno v:
Journal of Medical Ethics and History of Medicine, Vol 17 (2024)
Complementary and alternative medicine (CAM) is a rapidly growing industry, with millions worldwide seeking these treatments for various ailments. While many CAM therapies have shown promise in improving health outcomes, there are also ethical challe
Externí odkaz:
https://doaj.org/article/e1f59fec2d9443ad9e723e95b2b432c2
Autor:
Tahereh Ashraf Ganjooei, Zanbagh Pirastehfar, Asieh Mosallanejad, Masoomeh Raoufi, Noushin Afshar Moghaddam, Mozhgan Hashemieh
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15‐year‐old
Externí odkaz:
https://doaj.org/article/19deb52ec67f4433b7c3d3b00728cbf7
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Due to the rarity of this disorder, paying attention to diagnostic clues is important. Low valine formula seems to be effective in improvement of patient's symptoms. Prevention of consanguineous marriage is the best way to prevent this disea
Externí odkaz:
https://doaj.org/article/542a5e82c5934621a83a98eb750dab4d
Autor:
Asieh Mosallanejad, Shahrzad Tabatabai, Marjan Shakiba, Mohammad Reza Alaei, Hedieh Saneifard
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 11, Pp SD07-SD08 (2016)
Ovarian hyperstimulation syndrome is a rare disease among preterm infants. This syndrome was first described in 1985 in four infants with a gestational age of
Externí odkaz:
https://doaj.org/article/c6c2e5f466a14808970550e715a9e4a9
Autor:
Asieh Mosallanejad, Fatemeh Sayarifard, Sima Hosseinverdi, Farzaneh Abbasi, Hosein Shabni Mirzaee, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 53, Iss 12 (2015)
There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal neuroma. The result of karyotype showed 47XX, with ex
Externí odkaz:
https://doaj.org/article/2983c0cbc92d41a9ae6dfc97199d6e10
Autor:
Masoud Movahedi, Marzieh Tavakol, Armin Hirbod-Mobarakeh, Mohammad Gharagozlou, Asghar Aghamohammadi, Zahra Tavakol, Kaveh Momenzadeh, Mohammad Nabavi, Abbas Dabbaghzade, Asieh Mosallanejad, Nima Rezaei
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 14, Iss 2 (2015)
Chronic urticaria is the most common skin diseases, characterized by chronic cutaneous lesions which severely debilitates patients in several aspects of their everyday life. Vitamin D is known to exert several actions in the immune system and to infl
Externí odkaz:
https://doaj.org/article/c0ea321f8a174d33b8135cf8b7d7d538
Autor:
Ali Sheikhy, Zahra Eydian, Aida Fallahzadeh, Marjan Shakiba, Mahmoud Hajipour, Mohammadreza Alaei, Asieh Mosallanejad, Hedyeh Saneifard
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(4)
Objectives Metabolic control during puberty is impaired in Type 1 Diabetes Mellitus (T1DM) patients due to increased insulin resistance. Metformin is one of the oral medications typically used in type 2 diabetes mellitus to reduce insulin resistance.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee68af6ad8c1f82f69a1d7c1c8b8e9df
https://pubmed.ncbi.nlm.nih.gov/35249270
https://pubmed.ncbi.nlm.nih.gov/35249270
Autor:
Ghamartaj Khanbabaee, Saleheh Tajalli, Marjan Shakiba, Mohammad Reza Khalilian, Hedyeh Saneifard, Mojtaba Lotfi, Asieh Mosallanejad, Mohammad Reza Alaei
Publikováno v:
Iranian Journal of Pediatrics. 31
Background: Morquio A, an autosomal recessive lysosomal storage disease, is caused by a defect in the enzyme N-acetyl-galactosamine-6-sulfatase. This leads to the accumulation of the glycosaminoglycans chondroitin-6-sulfate (C6S) and keratan sulfate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f18b9c44c0bb49527474e25c740aab
https://doi.org/10.5812/ijp.111562
https://doi.org/10.5812/ijp.111562