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Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy.

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Title: Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy.
Authors: Naderian, Ramtin1,2 (AUTHOR), Vafaeian, Farzane3 (AUTHOR), Hoseini, Seyyed Mohamad3 (AUTHOR) Dr.hoseini8700@gmail.com, Sanami, Samira4 (AUTHOR) samirasanami34@yahoo.com
Source: BMC Neurology. 5/29/2025, Vol. 25 Issue 1, p1-6. 6p.
Database: Academic Search Ultimate
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  Data: Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy.
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  Data: <searchLink fieldCode="AR" term="%22Naderian%2C+Ramtin%22">Naderian, Ramtin</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vafaeian%2C+Farzane%22">Vafaeian, Farzane</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hoseini%2C+Seyyed+Mohamad%22">Hoseini, Seyyed Mohamad</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> Dr.hoseini8700@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Sanami%2C+Samira%22">Sanami, Samira</searchLink><relatesTo>4</relatesTo> (AUTHOR)<i> samirasanami34@yahoo.com</i>
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  Data: <searchLink fieldCode="JN" term="%22BMC+Neurology%22">BMC Neurology</searchLink>. 5/29/2025, Vol. 25 Issue 1, p1-6. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=185521028
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      – Type: doi
        Value: 10.1186/s12883-025-04253-x
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      – Code: eng
        Text: English
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      – TitleFull: Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy.
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            NameFull: Naderian, Ramtin
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            NameFull: Vafaeian, Farzane
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            NameFull: Hoseini, Seyyed Mohamad
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              Text: 5/29/2025
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              Y: 2025
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