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M Valente

Showing results (671-680 of 945) with videos related to

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Annals of Neurology|October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic studyO Bandmann, E M Valente, P Holmans, et al.
Techniques in Coloproctology|November 15, 2022
What is the real morbidity after emergency colectomy for Crohn's disease? A propensity score matched studyT M Connelly, C Clancy, J Y Cheong, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
A family study on primary blepharospasmG Defazio, D Martino, M S Aniello, et al.
Arquivos De Neuro-Psiquiatria|December 16, 1998
[Glutaric aciduria type 1: phenotypic variability. Report of 6 patients]E B Casella, A U Bresolin, M Valente, et al.
Il Giornale Di Chirurgia|December 7, 2005
[Giant mucocele of appendix. Case report]M Pittaluga, R Lombezzi, G Fantino, et al.
Journal of Medical Genetics|February 4, 2005
NPHP1 gene deletion is a rare cause of Joubert syndrome related disordersM Castori, E M Valente, M A Donati, et al.
Journal of Agricultural and Food Chemistry|January 28, 2009
Preparation of achiral and chiral (E)-enaminopyran-2,4-diones and their phytotoxic activityLuiz C Dias, Antônio J Demuner, Vânia M M Valente, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4AF Brancati, E M Valente, N P Davies, et al.
Thorax|March 18, 2008
Overexpression of squamous cell carcinoma antigen in idiopathic pulmonary fibrosis: clinicopathological correlationsF Calabrese, F Lunardi, C Giacometti, et al.
Kidney International|August 11, 2006
Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the associationG Caridi, M Dagnino, A Rossi, et al.
Pageof 95

Showing results (671-680 of 945) with videos related to

Sort By:
Pageof 95
Annals of Neurology|October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic studyO Bandmann, E M Valente, P Holmans, et al.
Techniques in Coloproctology|November 15, 2022
What is the real morbidity after emergency colectomy for Crohn's disease? A propensity score matched studyT M Connelly, C Clancy, J Y Cheong, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
A family study on primary blepharospasmG Defazio, D Martino, M S Aniello, et al.
Arquivos De Neuro-Psiquiatria|December 16, 1998
[Glutaric aciduria type 1: phenotypic variability. Report of 6 patients]E B Casella, A U Bresolin, M Valente, et al.
Il Giornale Di Chirurgia|December 7, 2005
[Giant mucocele of appendix. Case report]M Pittaluga, R Lombezzi, G Fantino, et al.
Journal of Medical Genetics|February 4, 2005
NPHP1 gene deletion is a rare cause of Joubert syndrome related disordersM Castori, E M Valente, M A Donati, et al.
Journal of Agricultural and Food Chemistry|January 28, 2009
Preparation of achiral and chiral (E)-enaminopyran-2,4-diones and their phytotoxic activityLuiz C Dias, Antônio J Demuner, Vânia M M Valente, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4AF Brancati, E M Valente, N P Davies, et al.
Thorax|March 18, 2008
Overexpression of squamous cell carcinoma antigen in idiopathic pulmonary fibrosis: clinicopathological correlationsF Calabrese, F Lunardi, C Giacometti, et al.
Kidney International|August 11, 2006
Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the associationG Caridi, M Dagnino, A Rossi, et al.
Pageof 95