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L Badia

Showing results (31-40 of 43) with videos related to

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Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
Sangre|January 1, 1977
[Multiple myeloma transforming into acute leukaemia (author's transl)]J Mayans, J Redon, L Badia, et al.
Clinical Mass Spectrometry (Del Mar, Calif.)|August 28, 2024
Multiplexed therapeutic drug monitoring (TDM) of antiviral drugs by LC-MS/MSM Conti, T Matulli Cavedagna, E Ramazzotti, et al.
Revue Neurologique|September 17, 2019
Motor neuron disease with leukodystrophy due to CSF1R mutationP V S Souza, B M L Badia, L H L Silva, et al.
Revue Neurologique|September 17, 2019
Rapidly progressive bulbar-onset ALS due to SS18L1 mutationW B V R Pinto, L H L Silva, B M L Badia, et al.
Revue Neurologique|June 1, 2019
SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotypeP V S Souza, L H L Silva, B M L Badia, et al.
Revue Neurologique|November 24, 2022
Expanding the spectrum of TBK1-related disorders: Adult-onset non-5q spinal muscular atrophyW B V R Pinto, P V S Souza, I B Farias, et al.
European Journal of Neurology|October 22, 2020
Clinical and radiological profile of patients with spinal muscular atrophy type 4P V S Souza, W B V R Pinto, A Ricarte, et al.
Mitochondrion|July 5, 2019
Leigh syndrome caused by mitochondrial DNA-maintenance defects revealed by whole exome sequencingP V S Souza, Thiago Bortholin, Carlos Alberto Castro Teixeira, et al.
Journal of Viral Hepatitis|December 16, 2016
Safety and efficacy of direct-acting antivirals for the treatment of chronic hepatitis C in a real-world population aged 65 years and olderF Conti, S Brillanti, F Buonfiglioli, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
Sangre|January 1, 1977
[Multiple myeloma transforming into acute leukaemia (author's transl)]J Mayans, J Redon, L Badia, et al.
Clinical Mass Spectrometry (Del Mar, Calif.)|August 28, 2024
Multiplexed therapeutic drug monitoring (TDM) of antiviral drugs by LC-MS/MSM Conti, T Matulli Cavedagna, E Ramazzotti, et al.
Revue Neurologique|September 17, 2019
Motor neuron disease with leukodystrophy due to CSF1R mutationP V S Souza, B M L Badia, L H L Silva, et al.
Revue Neurologique|September 17, 2019
Rapidly progressive bulbar-onset ALS due to SS18L1 mutationW B V R Pinto, L H L Silva, B M L Badia, et al.
Revue Neurologique|June 1, 2019
SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotypeP V S Souza, L H L Silva, B M L Badia, et al.
Revue Neurologique|November 24, 2022
Expanding the spectrum of TBK1-related disorders: Adult-onset non-5q spinal muscular atrophyW B V R Pinto, P V S Souza, I B Farias, et al.
European Journal of Neurology|October 22, 2020
Clinical and radiological profile of patients with spinal muscular atrophy type 4P V S Souza, W B V R Pinto, A Ricarte, et al.
Mitochondrion|July 5, 2019
Leigh syndrome caused by mitochondrial DNA-maintenance defects revealed by whole exome sequencingP V S Souza, Thiago Bortholin, Carlos Alberto Castro Teixeira, et al.
Journal of Viral Hepatitis|December 16, 2016
Safety and efficacy of direct-acting antivirals for the treatment of chronic hepatitis C in a real-world population aged 65 years and olderF Conti, S Brillanti, F Buonfiglioli, et al.
Pageof 5