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1.
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy.
J Med Genet
; 53(12): 850-858, 2016 12.
Article
in English
| MEDLINE | ID: mdl-27358180
2.
Co-occurrence of infantile epileptic seizures and childhood paroxysmal choreoathetosis in one family: clinical, EEG, and SPECT characterization of episodic events.
Mov Disord
; 17(1): 98-104, 2002 Jan.
Article
in English
| MEDLINE | ID: mdl-11835445
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