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Journal of Neurology
|
September 3, 2014
NADPH oxidase (NOX2) activity is a modifier of survival in ALS
Giuseppe Marrali, Federico Casale, Paolina Salamone, et al.
Reproductive Biomedicine Online
|
March 27, 2019
Inferring biallelism of two FSH receptor mutations associated with spontaneous ovarian hyperstimulation syndrome by evaluating FSH, LH and HCG cross-activity
Clara Lazzaretti, Laura Riccetti, Samantha Sperduti, et al.
Annals of the New York Academy of Sciences
|
November 17, 2006
Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCR
Silvia Galbiati, Gabriella Restagno, Barbara Foglieni, et al.
Neurology
|
October 27, 2012
Extensive genetics of ALS: a population-based study in Italy
Adriano Chiò, Andrea Calvo, Letizia Mazzini, et al.
Journal of Medical Screening
|
August 13, 1999
Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosis
P Gasparini, E Arbustini, G Restagno, et al.
Journal of Neurotrauma
|
October 6, 2006
In vivo characterization of traumatic brain injury neuropathology with structural and functional neuroimaging
Brian Levine, Esther Fujiwara, Charlene O'Connor, et al.
Clinical Chemistry
|
November 26, 2002
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology
Rosa Santacroce, Antonia Ratti, Francesco Caroli, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 22, 2014
The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients
Angelina Cistaro, Marco Pagani, Anna Montuschi, et al.
Neurobiology of Aging
|
May 20, 2009
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
Adriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Archives of Neurology
|
August 11, 2010
Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations
Adriano Chiò, Andrea Calvo, Cristina Moglia, et al.
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of 17
Search research articles
Search
Showing results (121-130 of 166) with videos related to
Sort By:
Page
of 17
Journal of Neurology
|
September 3, 2014
NADPH oxidase (NOX2) activity is a modifier of survival in ALS
Giuseppe Marrali, Federico Casale, Paolina Salamone, et al.
Reproductive Biomedicine Online
|
March 27, 2019
Inferring biallelism of two FSH receptor mutations associated with spontaneous ovarian hyperstimulation syndrome by evaluating FSH, LH and HCG cross-activity
Clara Lazzaretti, Laura Riccetti, Samantha Sperduti, et al.
Annals of the New York Academy of Sciences
|
November 17, 2006
Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCR
Silvia Galbiati, Gabriella Restagno, Barbara Foglieni, et al.
Neurology
|
October 27, 2012
Extensive genetics of ALS: a population-based study in Italy
Adriano Chiò, Andrea Calvo, Letizia Mazzini, et al.
Journal of Medical Screening
|
August 13, 1999
Analysis of 31 CFTR mutations by polymerase chain reaction/oligonucleotide ligation assay in a pilot screening of 4476 newborns for cystic fibrosis
P Gasparini, E Arbustini, G Restagno, et al.
Journal of Neurotrauma
|
October 6, 2006
In vivo characterization of traumatic brain injury neuropathology with structural and functional neuroimaging
Brian Levine, Esther Fujiwara, Charlene O'Connor, et al.
Clinical Chemistry
|
November 26, 2002
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology
Rosa Santacroce, Antonia Ratti, Francesco Caroli, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 22, 2014
The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients
Angelina Cistaro, Marco Pagani, Anna Montuschi, et al.
Neurobiology of Aging
|
May 20, 2009
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
Adriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Archives of Neurology
|
August 11, 2010
Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations
Adriano Chiò, Andrea Calvo, Cristina Moglia, et al.
Page
of 17