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Gerald M Fenichel

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Adolescent Medicine (Philadelphia, Pa.)|September 25, 2002
Neurocutaneous syndromesDina Dahan, Gerald M Fenichel, Refaat El-Said
Archives of Neurology|October 13, 2004
Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegiaPeter Hedera, Gerald M Fenichel, Marcia Blair, et al.
Seizure|August 19, 2007
Levetiracetam monotherapy in juvenile myoclonic epilepsyDeron V Sharpe, Anup D Patel, Bassel Abou-Khalil, et al.
Journal of Neuropathology and Experimental Neurology|October 6, 2006
Limb-girdle muscular dystrophy in the United StatesSteven A Moore, Christopher J Shilling, Steven Westra, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Adolescent Medicine (Philadelphia, Pa.)|September 25, 2002
Neurocutaneous syndromesDina Dahan, Gerald M Fenichel, Refaat El-Said
Archives of Neurology|October 13, 2004
Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegiaPeter Hedera, Gerald M Fenichel, Marcia Blair, et al.
Seizure|August 19, 2007
Levetiracetam monotherapy in juvenile myoclonic epilepsyDeron V Sharpe, Anup D Patel, Bassel Abou-Khalil, et al.
Journal of Neuropathology and Experimental Neurology|October 6, 2006
Limb-girdle muscular dystrophy in the United StatesSteven A Moore, Christopher J Shilling, Steven Westra, et al.
Pageof 1