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Denia Ramirez-Montealegre

Showing results (1-10 of 13) with videos related to

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Human Molecular Genetics|October 28, 2005
Defective lysosomal arginine transport in juvenile Batten diseaseDenia Ramirez-Montealegre, David A Pearce
Neurology|August 8, 2007
Imaging of late infantile neuronal ceroid lipofuscinosis: a clinical rating scaleDenia Ramirez-Montealegre, David A Pearce
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2003
A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten diseaseYoojin Kim, Denia Ramirez-Montealegre, David A Pearce
Brain : a Journal of Neurology|June 2, 2006
Another disorder finds its geneDenia Ramirez-Montealegre, Paul G Rothberg, David A Pearce
Pediatric Radiology|October 13, 2017
Enhancement of multiple cranial and spinal nerves in vanishing white matter: expanding the differential diagnosisThomas Jose Eluvathingal Muttikkal, Denia Ramirez Montealegre, Julie Ann Matsumoto
Survey of Ophthalmology|June 23, 2009
Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eyeSara Bozorg, Denia Ramirez-Montealegre, Mina Chung, et al.
The Journal of Molecular Diagnostics : JMD|July 23, 2004
Homogeneous polymerase chain reaction nucleobase quenching assay to detect the 1-kbp deletion in CLN3 that causes Batten diseasePaul G Rothberg, Denia Ramirez-Montealegre, Sharon D Frazier, et al.
Pediatric Neurology|February 9, 2017
Acute Disseminated Encephalomyelitis: A Gray DistinctionAmal Abu Libdeh, Howard P Goodkin, Denia Ramirez-Montealegre, et al.
Nature Reviews. Neurology|February 21, 2019
Therapeutic landscape for Batten disease: current treatments and future prospectsTyler B Johnson, Jacob T Cain, Katherine A White, et al.
Developmental Medicine and Child Neurology|March 18, 2006
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosisHeather Adams, Elisabeth A de Blieck, Jonathan W Mink, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|October 28, 2005
Defective lysosomal arginine transport in juvenile Batten diseaseDenia Ramirez-Montealegre, David A Pearce
Neurology|August 8, 2007
Imaging of late infantile neuronal ceroid lipofuscinosis: a clinical rating scaleDenia Ramirez-Montealegre, David A Pearce
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2003
A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten diseaseYoojin Kim, Denia Ramirez-Montealegre, David A Pearce
Brain : a Journal of Neurology|June 2, 2006
Another disorder finds its geneDenia Ramirez-Montealegre, Paul G Rothberg, David A Pearce
Pediatric Radiology|October 13, 2017
Enhancement of multiple cranial and spinal nerves in vanishing white matter: expanding the differential diagnosisThomas Jose Eluvathingal Muttikkal, Denia Ramirez Montealegre, Julie Ann Matsumoto
Survey of Ophthalmology|June 23, 2009
Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eyeSara Bozorg, Denia Ramirez-Montealegre, Mina Chung, et al.
The Journal of Molecular Diagnostics : JMD|July 23, 2004
Homogeneous polymerase chain reaction nucleobase quenching assay to detect the 1-kbp deletion in CLN3 that causes Batten diseasePaul G Rothberg, Denia Ramirez-Montealegre, Sharon D Frazier, et al.
Pediatric Neurology|February 9, 2017
Acute Disseminated Encephalomyelitis: A Gray DistinctionAmal Abu Libdeh, Howard P Goodkin, Denia Ramirez-Montealegre, et al.
Nature Reviews. Neurology|February 21, 2019
Therapeutic landscape for Batten disease: current treatments and future prospectsTyler B Johnson, Jacob T Cain, Katherine A White, et al.
Developmental Medicine and Child Neurology|March 18, 2006
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosisHeather Adams, Elisabeth A de Blieck, Jonathan W Mink, et al.
Pageof 2