Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Reihaneh, Mohsenipour"'
Autor:
Reihaneh Mohsenipour, Majid Aflatoonian, Hossein Alimadadi, Parisa Rahmani, Nazanin Esmaeili, Mohammad Yazdi, Farzaneh Abbasi, Fatemeh Solgi, Farshad Sharifi, Nahid Vafaii, Ali Mohebbi, Maryam Khazdouz
Publikováno v:
BMC Gastroenterology, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Chronic abdominal pain is a potential symptom of lead poisoning, which is often challenging to diagnose. This case–control study aimed to evaluate blood lead levels in pediatric patients with chronic abdominal pain. Methods The
Externí odkaz:
https://doaj.org/article/fb8a6c2fbcf14e928fe77924ab0170cc
Autor:
Payman Sadeghi, Golnaz Ghazizadeh Esslami, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Reihaneh Mohsenipour
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease characterized by some clinical signs (e.g., non-remitting fever, hepatosplenomegaly) and laboratory findings (e.g., cytopenia, increased ferritin level, hypofi
Externí odkaz:
https://doaj.org/article/ee55f422fdc14bd685c425f2b55b26af
Publikováno v:
International Journal of Nutrition Sciences, Vol 7, Iss 2, Pp 94-99 (2022)
Background: Total parenteral nutrition (TPN) is used to maintain the nutritional status of children in surgical wards which is essential not only for patients’ recovery, but also for normal growth and development. Given the high prevalence of TPN i
Externí odkaz:
https://doaj.org/article/fa2686f7665c4d179ca2c943763633b5
Autor:
Parisa Rahmani, Mohammad Roshanghalb, Hosein Alimadadi, Behnaz Bazargani, Nasir Fakhar, Reihaneh Mohsenipour
Publikováno v:
Tehran University Medical Journal, Vol 78, Iss 8, Pp 510-514 (2020)
Background: CNS infection can be focal or generalized. Meningitis, besides other etiologies, can occur after a viral infection or viral vaccine. Although meningitis can occur in at any age but it is more common in children less than five years old. A
Externí odkaz:
https://doaj.org/article/af62e8f8a5834d98b97095a0ca858954
Autor:
Ziba Mosayebi, Mohammadreza Mirzaaghayan, Reza Shabanian, Behdad Gharib, Elahe Movahedi, minoo dadkhah, Reihaneh Mohsenipour, Maryam Saeedi
Publikováno v:
Iranian Journal of Neonatology, Vol 11, Iss 2, Pp 112-116 (2020)
Background: Neonatal thrombotic diseases can cause mortality or serious morbidity and disability.Case report: In this report, we present a case of neonatal inferior vena cava thromboembolism with several underlyingfactors. Hereditary thrombophilia an
Externí odkaz:
https://doaj.org/article/c24b4ca1e89140bdbbfccd07b08842e2
Autor:
Reza Shervin Badv, Sara Memarian, Masoud Ghahvechi, Hossein Farshad Moghaddam, Maryam Saidi, Reihaneh Mohsenipour, Parisa Rahmani, Bahram Yarali, Mojtaba Gorji, Behdad Gharib
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 4, Iss 12, Pp 35-38 (2018)
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of
Externí odkaz:
https://doaj.org/article/fb28ad3022b04b1db09af02ae2d97dbe
Publikováno v:
J Diabetes Metab Disord
BACKGROUND: Obesity is a complicated phenomenon which is a combination of genetic, environmental, and psychological factors. Genetic factors of obesity play an important role in individual risk. It is well known that obese children have disturbed pub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1d08141ef372d8c9e523172c9afd3b
https://doi.org/10.1007/s40200-022-01011-5
https://doi.org/10.1007/s40200-022-01011-5
Autor:
Nima Rezaei, Reihaneh Mohsenipour, Parisa Tajdini, Fatemeh Sayarifard, Hamid Reza Khoramkhorshid, Sedigheh Madani
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 21:2296-2299
Background: In Congenital Disorder of Glycosylation (CDG) type Ia, homozygous mutations of the PMM2 gene cause phosphomannomutase 2 dysfunction. Case presentation: Herein, a 10-month-old girl is presented with severe hypotonia along with inappropriat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08fc92b86c3772f9b89ec607e63f8294
https://doi.org/10.2174/1871530321666210415105917
https://doi.org/10.2174/1871530321666210415105917
Autor:
Elmira Haji Esmaeli Memar, Reihaneh Mohsenipour, Seyedeh Taravat Sadrosadat, Parastoo Rostami
Publikováno v:
World Journal of Pediatrics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca07d5ec6440e614f553225099e05351
https://doi.org/10.1007/s12519-022-00662-x
https://doi.org/10.1007/s12519-022-00662-x
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 10 (2017)
Pericentric inversion of Chromosome 9 is one of the most common chromosomal abnormalities, which could be associated with various manifestations in some cases. Herein, a patient is presented with ambiguous genitalia that karyotyping revealed pericent
Externí odkaz:
https://doaj.org/article/9ccb883efa404322bebcfc867c2f9de4