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American Journal of Medical Genetics. Part A
|
August 23, 2019
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations
Marta Gatti, Stefania Magri, Lorenzo Nanetti, et al.
Talanta
|
October 31, 2008
Chemical profiling and classification of illicit heroin by principal component analysis, calculation of inter sample correlation and artificial neural networks
Pierre Esseiva, Frederic Anglada, Laurence Dujourdy, et al.
Neurobiology of Aging
|
March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling
Cinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neuroscience Letters
|
May 2, 2018
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients
Alessia Mongelli, Lidia Sarro, Elena Rizzo, et al.
Journal of the Neurological Sciences
|
May 1, 2019
Neuropsychological features of adult form of Alexander disease
Lara Draghi, Ettore Salsano, Laura Farina, et al.
Journal of Forensic Sciences
|
August 8, 2015
A Practical Guide for the Formulation of Propositions in the Bayesian Approach to DNA Evidence Interpretation in an Adversarial Environment
Simone Gittelson, Tim Kalafut, Steven Myers, et al.
Journal of Neuromuscular Diseases
|
May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literature
Elena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.
Frontiers in Genetics
|
December 27, 2016
Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent Concerns
Alex Biedermann, Christophe Champod, Graham Jackson, et al.
Journal of Neurochemistry
|
March 16, 2026
Neurotrophic Modulation Restores Motor and Developmental Defects in Zebrafish Models of ints11 Deficiency
Anna Pistocchi, Elena Chiricozzi, Matilde Molteni, et al.
Experimental Neurology
|
March 18, 2009
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference
Maria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, et al.
Page
of 21
Search research articles
Search
Showing results (91-100 of 204) with videos related to
Sort By:
Page
of 21
American Journal of Medical Genetics. Part A
|
August 23, 2019
From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations
Marta Gatti, Stefania Magri, Lorenzo Nanetti, et al.
Talanta
|
October 31, 2008
Chemical profiling and classification of illicit heroin by principal component analysis, calculation of inter sample correlation and artificial neural networks
Pierre Esseiva, Frederic Anglada, Laurence Dujourdy, et al.
Neurobiology of Aging
|
March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling
Cinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neuroscience Letters
|
May 2, 2018
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients
Alessia Mongelli, Lidia Sarro, Elena Rizzo, et al.
Journal of the Neurological Sciences
|
May 1, 2019
Neuropsychological features of adult form of Alexander disease
Lara Draghi, Ettore Salsano, Laura Farina, et al.
Journal of Forensic Sciences
|
August 8, 2015
A Practical Guide for the Formulation of Propositions in the Bayesian Approach to DNA Evidence Interpretation in an Adversarial Environment
Simone Gittelson, Tim Kalafut, Steven Myers, et al.
Journal of Neuromuscular Diseases
|
May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literature
Elena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.
Frontiers in Genetics
|
December 27, 2016
Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent Concerns
Alex Biedermann, Christophe Champod, Graham Jackson, et al.
Journal of Neurochemistry
|
March 16, 2026
Neurotrophic Modulation Restores Motor and Developmental Defects in Zebrafish Models of ints11 Deficiency
Anna Pistocchi, Elena Chiricozzi, Matilde Molteni, et al.
Experimental Neurology
|
March 18, 2009
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference
Maria Stella Lombardi, Leonie Jaspers, Christine Spronkmans, et al.
Page
of 21