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Diana Rodriguez

Showing results (101-110 of 193) with videos related to

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The Journal of Investigative Dermatology|April 30, 2010
NF-1Score: a prediction score for internal neurofibromas in neurofibromatosis-1Emilie Sbidian, Pierre Wolkenstein, Laurence Valeyrie-Allanore, et al.
European Journal of Medical Genetics|January 14, 2009
POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.
Parkinsonism & Related Disorders|February 5, 2025
Atypical ADCY5-related movement disorders: Highlighting adolescent/adult-onset cervical dystoniaFloriane Quazza, Florence Riant, Martina Patera, et al.
Nefrologia|June 18, 2024
Correlation of plasmatic sodium determined by the laboratory and that determined by the dialysis machineJoaquim Casals, José Jesús Broseta, Rosa María Fernández, et al.
Annals of Neurology|February 26, 2003
Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathyMichael E Shy, Grace Hobson, Manisha Jain, et al.
Orphanet Journal of Rare Diseases|May 6, 2011
Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in FranceTu Anh Duong, Emilie Sbidian, Laurence Valeyrie-Allanore, et al.
Experimental Cell Research|July 3, 2007
Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander diseaseCyril Mignot, Cécile Delarasse, Séverine Escaich, et al.
Brain & Development|April 7, 2007
Early neurological phenotype in 4 children with biallelic PRODH mutationsAlexandra Afenjar, Marie-Laure Moutard, Diane Doummar, et al.
Annals of Neurology|July 28, 2005
Dominant form of vanishing white matter-like leukoencephalopathyPierre Labauge, Anne Fogli, Giovanni Castelnovo, et al.
Frontiers in Neurology|June 15, 2026
Highlighting the value of polymyography in childhood onset movement disordersRaffaella Moretti, Claudia Ravelli, Yara Ahmar, et al.
Pageof 20

Showing results (101-110 of 193) with videos related to

Sort By:
Pageof 20
The Journal of Investigative Dermatology|April 30, 2010
NF-1Score: a prediction score for internal neurofibromas in neurofibromatosis-1Emilie Sbidian, Pierre Wolkenstein, Laurence Valeyrie-Allanore, et al.
European Journal of Medical Genetics|January 14, 2009
POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.
Parkinsonism & Related Disorders|February 5, 2025
Atypical ADCY5-related movement disorders: Highlighting adolescent/adult-onset cervical dystoniaFloriane Quazza, Florence Riant, Martina Patera, et al.
Nefrologia|June 18, 2024
Correlation of plasmatic sodium determined by the laboratory and that determined by the dialysis machineJoaquim Casals, José Jesús Broseta, Rosa María Fernández, et al.
Annals of Neurology|February 26, 2003
Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathyMichael E Shy, Grace Hobson, Manisha Jain, et al.
Orphanet Journal of Rare Diseases|May 6, 2011
Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in FranceTu Anh Duong, Emilie Sbidian, Laurence Valeyrie-Allanore, et al.
Experimental Cell Research|July 3, 2007
Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander diseaseCyril Mignot, Cécile Delarasse, Séverine Escaich, et al.
Brain & Development|April 7, 2007
Early neurological phenotype in 4 children with biallelic PRODH mutationsAlexandra Afenjar, Marie-Laure Moutard, Diane Doummar, et al.
Annals of Neurology|July 28, 2005
Dominant form of vanishing white matter-like leukoencephalopathyPierre Labauge, Anne Fogli, Giovanni Castelnovo, et al.
Frontiers in Neurology|June 15, 2026
Highlighting the value of polymyography in childhood onset movement disordersRaffaella Moretti, Claudia Ravelli, Yara Ahmar, et al.
Pageof 20