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G Scarano

Showing results (51-60 of 63) with videos related to

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Journal of Endocrinological Investigation|July 19, 2023
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveysM F Bedeschi, S Mora, F Antoniazzi, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
Assessing the memorization of TV commercials with the use of high resolution EEG: a pilot studyL Astolfi, R Soranzo, F Cincotti, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Case Reports in Medicine|July 26, 2019
Kounis Syndrome as First Manifestation of Allergic SensitizationD Forlani, G Scarano, A D'Alleva, et al.
Clinical Genetics|November 13, 2014
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patientsS Spena, D Milani, D Rusconi, et al.
Clinical Genetics|July 31, 2007
Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutationA Selicorni, S Russo, C Gervasini, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Clinical Genetics|May 31, 2017
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOHA Vetro, D Goidin, I Lesende, et al.
Journal of Medical Genetics|February 5, 2003
SHOX mutations detected by FISH and direct sequencing in patients with short statureL Stuppia, G Calabrese, V Gatta, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Journal of Endocrinological Investigation|July 19, 2023
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveysM F Bedeschi, S Mora, F Antoniazzi, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
Assessing the memorization of TV commercials with the use of high resolution EEG: a pilot studyL Astolfi, R Soranzo, F Cincotti, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Case Reports in Medicine|July 26, 2019
Kounis Syndrome as First Manifestation of Allergic SensitizationD Forlani, G Scarano, A D'Alleva, et al.
Clinical Genetics|November 13, 2014
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patientsS Spena, D Milani, D Rusconi, et al.
Clinical Genetics|July 31, 2007
Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutationA Selicorni, S Russo, C Gervasini, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Clinical Genetics|May 31, 2017
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOHA Vetro, D Goidin, I Lesende, et al.
Journal of Medical Genetics|February 5, 2003
SHOX mutations detected by FISH and direct sequencing in patients with short statureL Stuppia, G Calabrese, V Gatta, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 7