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R Militerni

Showing results (1-10 of 12) with videos related to

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European Journal of Endocrinology|July 31, 1999
Intellectual outcome at 12 years of age in congenital hypothyroidismM Salerno, R Militerni, S Di Maio, et al.
Journal of Endocrinological Investigation|November 1, 1995
Prognostic factors in the intellectual development at 7 years of age in children with congenital hypothyroidismM Salerno, S Di Maio, R Militerni, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1982
[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?]M M Rinaldi, R Militerni, A Pascotto, et al.
American Journal of Medical Genetics|February 25, 2000
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samplesA M Persico, R Militerni, C Bravaccio, et al.
Psychiatric Genetics|August 30, 2001
No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorderA M Persico, R Militerni, C Bravaccio, et al.
American Journal of Medical Genetics|December 20, 2000
Adenosine deaminase alleles and autistic disorder: case-control and family-based association studiesA M Persico, R Militerni, C Bravaccio, et al.
Molecular Psychiatry|August 23, 2002
Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic childrenA M Persico, T Pascucci, S Puglisi-Allegra, et al.
Molecular Psychiatry|March 5, 2008
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expressionC Lintas, R Sacco, K Garbett, et al.
Psychiatric Genetics|May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probandsA M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry|July 9, 2008
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1L Palmieri, V Papaleo, V Porcelli, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Endocrinology|July 31, 1999
Intellectual outcome at 12 years of age in congenital hypothyroidismM Salerno, R Militerni, S Di Maio, et al.
Journal of Endocrinological Investigation|November 1, 1995
Prognostic factors in the intellectual development at 7 years of age in children with congenital hypothyroidismM Salerno, S Di Maio, R Militerni, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1982
[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?]M M Rinaldi, R Militerni, A Pascotto, et al.
American Journal of Medical Genetics|February 25, 2000
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samplesA M Persico, R Militerni, C Bravaccio, et al.
Psychiatric Genetics|August 30, 2001
No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorderA M Persico, R Militerni, C Bravaccio, et al.
American Journal of Medical Genetics|December 20, 2000
Adenosine deaminase alleles and autistic disorder: case-control and family-based association studiesA M Persico, R Militerni, C Bravaccio, et al.
Molecular Psychiatry|August 23, 2002
Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic childrenA M Persico, T Pascucci, S Puglisi-Allegra, et al.
Molecular Psychiatry|March 5, 2008
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expressionC Lintas, R Sacco, K Garbett, et al.
Psychiatric Genetics|May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probandsA M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry|July 9, 2008
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1L Palmieri, V Papaleo, V Porcelli, et al.
Pageof 2