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C Mariotti

Showing results (71-80 of 421) with videos related to

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Human Molecular Genetics|August 1, 1995
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) geneV Tiranti, P Chariot, F Carella, et al.
Journal of Pharmaceutical and Biomedical Analysis|July 4, 2018
Interval importance index to select relevant ATR-FTIR wavenumber Intervals for falsified drug classificationA Kahmann, M J Anzanello, F S Fogliatto, et al.
Pathologica|March 8, 2012
Breast cancer and primary systemic therapy. Results of the Consensus Meeting on the recommendations for pathological examination and histological report of breast cancer specimens in the Marche RegionA Santinelli, M De Nictolis, V Mambelli, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.
International Journal of Toxicology|March 13, 2012
Toxicological effects of a mixture used in weight loss products: p-synephrine associated with ephedrine, salicin, and caffeineGabriela C Schmitt, Marcelo D Arbo, Andréia L Lorensi, et al.
European Journal of Neurology|January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthoodB P C van de Warrenburg, J van Gaalen, S Boesch, et al.
European Neurology|July 1, 2010
Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring cliniciansC Mariotti, A Ferruta, C Gellera, et al.
Neurology|January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaA Brussino, C Gellera, A Saluto, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Analytica Chimica Acta|May 31, 2011
Determination of amphetamine-type stimulants in oral fluid by solid-phase microextraction and gas chromatography-mass spectrometryDaniele Z Souza, Paula O Boehl, Eloisa Comiran, et al.
Pageof 43

Showing results (71-80 of 421) with videos related to

Sort By:
Pageof 43
Human Molecular Genetics|August 1, 1995
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) geneV Tiranti, P Chariot, F Carella, et al.
Journal of Pharmaceutical and Biomedical Analysis|July 4, 2018
Interval importance index to select relevant ATR-FTIR wavenumber Intervals for falsified drug classificationA Kahmann, M J Anzanello, F S Fogliatto, et al.
Pathologica|March 8, 2012
Breast cancer and primary systemic therapy. Results of the Consensus Meeting on the recommendations for pathological examination and histological report of breast cancer specimens in the Marche RegionA Santinelli, M De Nictolis, V Mambelli, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.
International Journal of Toxicology|March 13, 2012
Toxicological effects of a mixture used in weight loss products: p-synephrine associated with ephedrine, salicin, and caffeineGabriela C Schmitt, Marcelo D Arbo, Andréia L Lorensi, et al.
European Journal of Neurology|January 15, 2014
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthoodB P C van de Warrenburg, J van Gaalen, S Boesch, et al.
European Neurology|July 1, 2010
Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring cliniciansC Mariotti, A Ferruta, C Gellera, et al.
Neurology|January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaA Brussino, C Gellera, A Saluto, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Analytica Chimica Acta|May 31, 2011
Determination of amphetamine-type stimulants in oral fluid by solid-phase microextraction and gas chromatography-mass spectrometryDaniele Z Souza, Paula O Boehl, Eloisa Comiran, et al.
Pageof 43