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Stefania Gianotti

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Epilepsia|September 30, 2005

Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutationBetul Baykan, Pasquale Striano, Stefania Gianotti, et al.

Epilepsia|April 23, 2004

Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: identification of a putative locus on chromosome 9q32-33Betül Baykan, Francesca Madia, Nerses Bebek, et al.

Computer Methods and Programs in Biomedicine|November 4, 2019

Texture analysis and multiple-instance learning for the classification of malignant lymphomasMarco Lippi, Stefania Gianotti, Angelo Fama, et al.

Nature Genetics|September 5, 2006

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractFederico Zara, Roberta Biancheri, Claudio Bruno, et al.

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Search research articles

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

Sort By:

Pageof 1

Epilepsia|September 30, 2005

Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutationBetul Baykan, Pasquale Striano, Stefania Gianotti, et al.

Epilepsia|April 23, 2004

Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: identification of a putative locus on chromosome 9q32-33Betül Baykan, Francesca Madia, Nerses Bebek, et al.

Computer Methods and Programs in Biomedicine|November 4, 2019

Texture analysis and multiple-instance learning for the classification of malignant lymphomasMarco Lippi, Stefania Gianotti, Angelo Fama, et al.

Nature Genetics|September 5, 2006

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractFederico Zara, Roberta Biancheri, Claudio Bruno, et al.

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