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Lorenzo Sinibaldi

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 31, 2015
Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers-Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revisedLorenzo Sinibaldi, Gianluca Ursini, Marco Castori
Attention Deficit and Hyperactivity Disorders|February 16, 2018
Attention-deficit/hyperactivity disorder, joint hypermobility-related disorders and pain: expanding body-mind connections to the developmental ageCarolina Baeza-Velasco, Lorenzo Sinibaldi, Marco Castori
Prenatal Diagnosis|April 26, 2005
Reproductive history of a healthy woman with mosaic duplication of chromosome 4pLaura Bernardini, Lorenzo Sinibaldi, Caterina Ceccarini, et al.
La Radiologia Medica|August 6, 2014
Quantitative ultrasound at the phalanges in a cohort of monozygotic twins of different agesGiuseppe Guglielmi, Francesca De Terlizzi, Michelangelo Nasuto, et al.
Prenatal Diagnosis|May 29, 2013
Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosisAnna Capalbo, Lorenzo Sinibaldi, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Duplication 18q21.31-q22.2Caterina Ceccarini, Lorenzo Sinibaldi, Laura Bernardini, et al.
Plos One|December 24, 2011
Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific bindingViviana Caputo, Lorenzo Sinibaldi, Alessia Fiorentino, et al.
European Journal of Human Genetics : EJHG|April 15, 2004
Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian familyAntonio Novelli, Enza Maria Valente, Laura Bernardini, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasAlessandro De Luca, Laura Bernardini, Caterina Ceccarini, et al.
Schizophrenia Research|July 24, 2007
COMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophreniaAlessandro Bertolino, Grazia Caforio, Giuseppe Blasi, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 31, 2015
Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/ Ehlers-Danlos syndrome, hypermobility type: The link between connective tissue and psychological distress revisedLorenzo Sinibaldi, Gianluca Ursini, Marco Castori
Attention Deficit and Hyperactivity Disorders|February 16, 2018
Attention-deficit/hyperactivity disorder, joint hypermobility-related disorders and pain: expanding body-mind connections to the developmental ageCarolina Baeza-Velasco, Lorenzo Sinibaldi, Marco Castori
Prenatal Diagnosis|April 26, 2005
Reproductive history of a healthy woman with mosaic duplication of chromosome 4pLaura Bernardini, Lorenzo Sinibaldi, Caterina Ceccarini, et al.
La Radiologia Medica|August 6, 2014
Quantitative ultrasound at the phalanges in a cohort of monozygotic twins of different agesGiuseppe Guglielmi, Francesca De Terlizzi, Michelangelo Nasuto, et al.
Prenatal Diagnosis|May 29, 2013
Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosisAnna Capalbo, Lorenzo Sinibaldi, Laura Bernardini, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Duplication 18q21.31-q22.2Caterina Ceccarini, Lorenzo Sinibaldi, Laura Bernardini, et al.
Plos One|December 24, 2011
Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific bindingViviana Caputo, Lorenzo Sinibaldi, Alessia Fiorentino, et al.
European Journal of Human Genetics : EJHG|April 15, 2004
Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian familyAntonio Novelli, Enza Maria Valente, Laura Bernardini, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasAlessandro De Luca, Laura Bernardini, Caterina Ceccarini, et al.
Schizophrenia Research|July 24, 2007
COMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophreniaAlessandro Bertolino, Grazia Caforio, Giuseppe Blasi, et al.
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