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Page 1
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Heidari A, Tongsook C, Najafipour R, Musante L, Vasli N, Garshasbi M, Hu H, Mittal K, McNaughton AJ, Sritharan K, Hudson M, Stehr H, Talebi S, Moradi M, Darvish H, Arshad Rafiq M, Mozhdehipanah H, Rashidinejad A, Samiei S, Ghadami M, Windpassinger C, Gillessen-Kaesbach G, Tzschach A, Ahmed I, Mikhailov A, Stavropoulos DJ, Carter MT, Keshavarz S, Ayub M, Najmabadi H, Liu X, Ropers HH, Macheroux P, Vincent JB. Heidari A, et al. Among authors: mozhdehipanah h. Hum Mol Genet. 2015 Oct 15;24(20):5697-710. doi: 10.1093/hmg/ddv286. Epub 2015 Jul 23. Hum Mol Genet. 2015. PMID: 26206890 Free PMC article.
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Harripaul R, Vasli N, Mikhailov A, Rafiq MA, Mittal K, Windpassinger C, Sheikh TI, Noor A, Mahmood H, Downey S, Johnson M, Vleuten K, Bell L, Ilyas M, Khan FS, Khan V, Moradi M, Ayaz M, Naeem F, Heidari A, Ahmed I, Ghadami S, Agha Z, Zeinali S, Qamar R, Mozhdehipanah H, John P, Mir A, Ansar M, French L, Ayub M, Vincent JB. Harripaul R, et al. Among authors: mozhdehipanah h. Mol Psychiatry. 2018 Apr;23(4):973-984. doi: 10.1038/mp.2017.60. Epub 2017 Apr 11. Mol Psychiatry. 2018. PMID: 28397838
Investigation of pregnancy tendency, reproductive characteristics, and disability in women with multiple sclerosis: A secondary data analysis of the national registry in Iran.
Ezabadi SG, Ashtari F, Baghbanian SM, Majdi-Nasab N, Madreseh E, Hatamian H, Faraji F, Bayati A, Kamali H, Sharifipour E, Mozhdehipanah H, Shahrbaf MA, Ayoubi S, Sahraian MA, Eskandarieh S. Ezabadi SG, et al. Among authors: mozhdehipanah h. Curr J Neurol. 2024 Apr 3;23(2):106-116. doi: 10.18502/cjn.v23i2.16839. Curr J Neurol. 2024. PMID: 39744653 Free PMC article.
Consanguineous marriage among familial multiple sclerosis subjects: A national registry-based study.
Salehi Z, Naghizadeh MM, Ezabadi SG, Ebrahimitirtashi A, Abbasi Kasbi N, Khodaie F, Aliyari S, Ashtari F, Baghbanian SM, Nabavi SM, Hosseini S, Razazian N, Shaygannejad V, Majdi-Nasab N, Harirchian MH, Bayati A, Kamali H, Hosseni Nejad Mir N, Beladi Moghadam N, Poursadeghfard M, Mozhdehipanah H, Jalali N, Nahayati MA, Faraji F, Kamyari N, Sahraian MA, Maghbooli Z, Eskandarieh S. Salehi Z, et al. Among authors: mozhdehipanah h. Heliyon. 2024 Jun 15;10(12):e32946. doi: 10.1016/j.heliyon.2024.e32946. eCollection 2024 Jun 30. Heliyon. 2024. PMID: 38984301 Free PMC article.
Time interval between the onset of symptoms and diagnosis of multiple sclerosis and the influential factors: A national registry-based study.
Khodaie F, Moghadasi AN, Hosseinnataj A, Baghbanian SM, Ashtari F, Razazian N, Poursadeghfard M, Majdi-Nasab N, Hatamian H, Hoseini S, Nahayati MA, Nabavi SM, Faraji F, Harirchian MH, Mir NHN, Moghadam NB, Sharifipour E, Bayati A, Kamali H, Mozhdehipanah H, Jalali N, Abotorabi-Zarchi M, Kamyari N, Nikbakht R, Azimi A, Navardi S, Heidari H, Sahraian MA, Eskandarieh S. Khodaie F, et al. Among authors: mozhdehipanah h. Clin Neurol Neurosurg. 2024 Apr;239:108221. doi: 10.1016/j.clineuro.2024.108221. Epub 2024 Mar 2. Clin Neurol Neurosurg. 2024. PMID: 38447483
Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene.
Rashvand Z, Najmabadi H, Kahrizi K, Mozhdehipanah H, Moradi M, Estaki Z, Taherkhani K, Nikzat N, Najafipour R, Omrani MD. Rashvand Z, et al. Among authors: mozhdehipanah h. Iran J Child Neurol. 2024 Winter;18(1):25-41. doi: 10.22037/ijcn.v18i1.42188. Epub 2024 Jan 18. Iran J Child Neurol. 2024. PMID: 38375126 Free PMC article.
Economic and Social Standing of Individuals in Iran Diagnosed with Multiple Sclerosis.
Ghadiri F, Sahraian MA, Ashtari F, Baghbanian SM, Majdi-Nasab N, Hatamian H, Faraji F, Bayati A, Sharifipour E, Jalali N, Mozhdehipanah H, Kamali H, Ayoubi S, Eskandarieh S, Naser Moghadasi A. Ghadiri F, et al. Among authors: mozhdehipanah h. Arch Iran Med. 2023 Aug 1;26(8):413-418. doi: 10.34172/aim.2023.63. Arch Iran Med. 2023. PMID: 38301102 Free PMC article.
Sex differences in cerebral venous sinus thrombosis after adenoviral vaccination against COVID-19.
Scutelnic A, van de Munckhof A, Krzywicka K, van Kammen MS, Lindgren E, Cordonnier C, Kleinig TJ, Field TS, Poli S, Lemmens R, Middeldorp S, Aaron S, Borhani-Haghighi A, Arauz A, Kremer Hovinga JA, Günther A, Putaala J, Wasay M, Conforto AB, de Sousa DA, Jood K, Tatlisumak T, Ferro JM, Coutinho JM, Arnold M, Heldner MR; Cerebral Venous Sinus Thrombosis with Thrombocytopenia Syndrome Study Group**. Scutelnic A, et al. Eur Stroke J. 2023 Dec;8(4):1001-1010. doi: 10.1177/23969873231185213. Epub 2023 Jul 11. Eur Stroke J. 2023. PMID: 37434312 Free PMC article.
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