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A Minassian

Showing results (161-170 of 324) with videos related to

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 13, 2007
Lafora-like ground-glass inclusions in hepatocytes of pediatric patients: a report of two casesAnne-Marie O'Shea, Gregory J Wilson, Simon C Ling, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 6, 2016
Lafora diseaseJulie Turnbull, Erica Tiberia, Pasquale Striano, et al.
International Journal of Antimicrobial Agents|June 13, 1998
A comparison between single-dose fosfomycin trometamol (Monuril) and a 5-day course of trimethoprim in the treatment of uncomplicated lower urinary tract infection in womenM A Minassian, D A Lewis, D Chattopadhyay, et al.
Archives of Biochemistry and Biophysics|November 23, 2006
Glycogen metabolism in tissues from a mouse model of Lafora diseaseWei Wang, Hannes Lohi, Alexander V Skurat, et al.
Canine Medicine and Genetics|December 28, 2021
Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United KingdomSaija Ahonen, Ian Seath, Clare Rusbridge, et al.
Urogynecology (Philadelphia, Pa.)|July 25, 2023
Treatment for Urinary Incontinence in Women Older Than 65 YearsGiulia I Lane, Elisabeth Erekson, Andrea Austin, et al.
Plos One|August 3, 2017
Lafora disease in miniature Wirehaired DachshundsLindsay Swain, Gill Key, Anna Tauro, et al.
Journal of Child Neurology|February 12, 2008
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolateJulie Turnbull, Santosh Kumar, Zhi-Ping Ren, et al.
Genome Medicine|June 1, 2017
Genome annotation for clinical genomic diagnostics: strengths and weaknessesCharles A Steward, Alasdair P J Parker, Berge A Minassian, et al.
Pediatric Neurology|December 3, 2014
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypesCyrus Boelman, Ana Marissa Lagman-Bartolome, Daune L MacGregor, et al.
Pageof 33

Showing results (161-170 of 324) with videos related to

Sort By:
Pageof 33
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 13, 2007
Lafora-like ground-glass inclusions in hepatocytes of pediatric patients: a report of two casesAnne-Marie O'Shea, Gregory J Wilson, Simon C Ling, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 6, 2016
Lafora diseaseJulie Turnbull, Erica Tiberia, Pasquale Striano, et al.
International Journal of Antimicrobial Agents|June 13, 1998
A comparison between single-dose fosfomycin trometamol (Monuril) and a 5-day course of trimethoprim in the treatment of uncomplicated lower urinary tract infection in womenM A Minassian, D A Lewis, D Chattopadhyay, et al.
Archives of Biochemistry and Biophysics|November 23, 2006
Glycogen metabolism in tissues from a mouse model of Lafora diseaseWei Wang, Hannes Lohi, Alexander V Skurat, et al.
Canine Medicine and Genetics|December 28, 2021
Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United KingdomSaija Ahonen, Ian Seath, Clare Rusbridge, et al.
Urogynecology (Philadelphia, Pa.)|July 25, 2023
Treatment for Urinary Incontinence in Women Older Than 65 YearsGiulia I Lane, Elisabeth Erekson, Andrea Austin, et al.
Plos One|August 3, 2017
Lafora disease in miniature Wirehaired DachshundsLindsay Swain, Gill Key, Anna Tauro, et al.
Journal of Child Neurology|February 12, 2008
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolateJulie Turnbull, Santosh Kumar, Zhi-Ping Ren, et al.
Genome Medicine|June 1, 2017
Genome annotation for clinical genomic diagnostics: strengths and weaknessesCharles A Steward, Alasdair P J Parker, Berge A Minassian, et al.
Pediatric Neurology|December 3, 2014
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypesCyrus Boelman, Ana Marissa Lagman-Bartolome, Daune L MacGregor, et al.
Pageof 33