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A Quattrone

Showing results (181-190 of 273) with videos related to

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Human Genetics|November 28, 2006
Gene symbol: MECP2. Disease: Rett syndromeF L Conforti, R Mazzei, T Sprovieri, et al.
Human Genetics|June 29, 2007
Gene symbol: NOTCH3R Mazzei, F L Conforti, C Ungaro, et al.
Human Genetics|June 29, 2007
Gene symbol: NOTCH3R Mazzei, F L Conforti, C Ungaro, et al.
Genes, Brain, and Behavior|May 30, 2009
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individualsA Cerasa, M C Gioia, P Tarantino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic lociC Rodolico, A Toscano, A Patitucci, et al.
Theriogenology|February 4, 2026
Effects of maternal feed restriction on placental lactogen and its correlation with pregnancy-associated glycoproteins in pregnant ewesO Barbato, V L Barile, L Menchetti, et al.
Human Genetics|November 28, 2006
Gene symbol: MECP2. Disease: Rett syndromeF L Conforti, R Mazzei, A Patitucci, et al.
Journal of Negative Results in Biomedicine|March 1, 2006
Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosisI Manna, P Valentino, A La Russa, et al.
Neurology|June 20, 1998
Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI studyR L Oliveri, P Valentino, C Russo, et al.
Epilepsia|December 28, 1999
Apolipoprotein E polymorphisms and the risk of nonlesional temporal lobe epilepsyA Gambardella, U Aguglia, R Cittadella, et al.
Pageof 28

Showing results (181-190 of 273) with videos related to

Sort By:
Pageof 28
Human Genetics|November 28, 2006
Gene symbol: MECP2. Disease: Rett syndromeF L Conforti, R Mazzei, T Sprovieri, et al.
Human Genetics|June 29, 2007
Gene symbol: NOTCH3R Mazzei, F L Conforti, C Ungaro, et al.
Human Genetics|June 29, 2007
Gene symbol: NOTCH3R Mazzei, F L Conforti, C Ungaro, et al.
Genes, Brain, and Behavior|May 30, 2009
The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individualsA Cerasa, M C Gioia, P Tarantino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic lociC Rodolico, A Toscano, A Patitucci, et al.
Theriogenology|February 4, 2026
Effects of maternal feed restriction on placental lactogen and its correlation with pregnancy-associated glycoproteins in pregnant ewesO Barbato, V L Barile, L Menchetti, et al.
Human Genetics|November 28, 2006
Gene symbol: MECP2. Disease: Rett syndromeF L Conforti, R Mazzei, A Patitucci, et al.
Journal of Negative Results in Biomedicine|March 1, 2006
Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosisI Manna, P Valentino, A La Russa, et al.
Neurology|June 20, 1998
Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI studyR L Oliveri, P Valentino, C Russo, et al.
Epilepsia|December 28, 1999
Apolipoprotein E polymorphisms and the risk of nonlesional temporal lobe epilepsyA Gambardella, U Aguglia, R Cittadella, et al.
Pageof 28