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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1998 1
2000 1
2004 1
2005 2
2006 6
2007 4
2008 2
2009 2
2010 3
2011 3
2012 5
2013 8
2014 7
2015 4
2016 6
2017 10
2018 7
2019 4
2020 4
2021 3
2022 4
2023 2
2024 3
2025 1
2026 2

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83 results

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Page 1
Rett syndrome.
Ghofrani M, Mahmoodian T. Ghofrani M, et al. Indian J Pediatr. 2000 Jul;67(7):539-40. doi: 10.1007/BF02760490. Indian J Pediatr. 2000. PMID: 10957842
Black thyroid syndrome.
Yusim A, Ghofrani M, Ocal IT, Roman S. Yusim A, et al. Among authors: ghofrani m. Thyroid. 2006 Aug;16(8):811-2. doi: 10.1089/thy.2006.16.811. Thyroid. 2006. PMID: 16910886 No abstract available.
Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities.
Kakar N, Mascarenhas S, Ali A, Azmatullah, Ijlal Haider SM, Badiger VA, Ghofrani MS, Kruse N, Hashmi SN, Pozojevic J, Balachandran S, Toft M, Malik S, Händler K, Fatima A, Iqbal Z, Shukla A, Spielmann M, Radhakrishnan P. Kakar N, et al. Among authors: ghofrani ms. Hum Genet. 2025 Jan;144(1):55-65. doi: 10.1007/s00439-024-02718-6. Epub 2024 Dec 21. Hum Genet. 2025. PMID: 39708122 Free PMC article.
Possible phenytoin-methylphenidate interaction.
Ghofrani M. Ghofrani M. Dev Med Child Neurol. 1988 Apr;30(2):267-8. doi: 10.1111/j.1469-8749.1988.tb04763.x. Dev Med Child Neurol. 1988. PMID: 3133263 No abstract available.
83 results