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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) gene
V 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 classification
A 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 Region
A 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 mutations
C 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 caffeine
Gabriela 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 adulthood
B 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 clinicians
C Mariotti, A Ferruta, C Gellera, et al.
Neurology
|
January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
A 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 families
C 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 spectrometry
Daniele Z Souza, Paula O Boehl, Eloisa Comiran, et al.
Page
of 43
Search research articles
Search
Showing results (71-80 of 421) with videos related to
Sort By:
Page
of 43
Human Molecular Genetics
|
August 1, 1995
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene
V 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 classification
A 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 Region
A 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 mutations
C 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 caffeine
Gabriela 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 adulthood
B 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 clinicians
C Mariotti, A Ferruta, C Gellera, et al.
Neurology
|
January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
A 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 families
C 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 spectrometry
Daniele Z Souza, Paula O Boehl, Eloisa Comiran, et al.
Page
of 43