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Jessica Cohen-Pfeffer
Jessica Cohen-Pfeffer
Disease
Cerliponase alfa
Genetics
Phenotype
Diabetes mellitus
4
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3
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0
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Clinical utility of a sponsored gene panel testing program for pediatric epilepsy and CLN2 disease diagnosis: Results from 4246 tests
2021
Molecular Genetics and Metabolism
Tiffany Yar Pang
Fernanda Leal-Pardinas
Rebecca Truty
Dianalee McKnight
Britt Johnson
Ana Morales
Sara L. Bristow
Emanuela Izzo
Jessica Cohen-Pfeffer
Raman Sankar
Sookyong Koh
Elaine C. Wirrell
John Millichap
Swaroop Aradhya
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Intracerebroventricular cerliponase alfa for CLN2 disease: Clinical practice considerations from US clinics
2020
Molecular Genetics and Metabolism
Raymond Y. Wang
Emily de los Reyes
Lenora Lehwald
Erika F. Augustine
Elizabeth Berry-Kravis
Karen Butler
Natalie Cormier
Scott Demarest
Sam Lu
Jacqueline Madden
Joffre Olaya
Susan See
Amy Vierhile
James W. Wheless
Amy C. Yang
Jessica Cohen-Pfeffer
Dorna Chu
Fernanda Leal-Pardinas
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Cerliponase Alfa for the Treatment of Atypical Phenotypes of CLN2 Disease: A Retrospective Case Series.
2020
Journal of Child Neurology
Eva Wibbeler
Raymond Y. Wang
Emily de los Reyes
Nicola Specchio
Paul Gissen
Norberto Guelbert
Miriam Nickel
Christoph Schwering
Lenora Lehwald
Marina Trivisano
Laura Lee
Gianni Amato
Jessica Cohen-Pfeffer
Renée Shediac
Fernanda Leal-Pardinas
Angela Schulz
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Cerliponase alfa for the treatment of atypical phenotypes of CLN2 disease: A retrospective case series
2020
Molecular Genetics and Metabolism
Eva Wibbeler
Raymond Y. Wang
Emily de los Reyes
Nicola Specchio
Paul Gissen
Norberto Guelbert
Miriam Nickel
Christoph Schwering
Lenora Lehwald
Marina Trivisano
Laura Lee
Gianni Amato
Jessica Cohen-Pfeffer
Renée Shediac
Fernanda Leal-Pardinas
Angela Schulz
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