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Michele Valiante

Showing results (1-10 of 21) with videos related to

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Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|January 26, 2017
Familial melanoma and multiple primary melanomaPaola DE Simone, Michele Valiante, Vitaliano Silipo
European Journal of Medical Genetics|September 3, 2013
Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature reviewMarco Castori, Michele Valiante, Giulia Pascolini, et al.
European Journal of Medical Genetics|June 24, 2020
Answer to Letter to the Editor regarding the article "Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion"Giulia Pascolini, Michele Valiante, Irene Bottillo, et al.
European Journal of Medical Genetics|August 18, 2019
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletionGiulia Pascolini, Michele Valiante, Irene Bottillo, et al.
Minerva Pediatrica|April 14, 2018
Incidental finding of an Xq microdeletion in a girl with trichorhinophalangeal syndrome type I harboring a novel TRPS1 nonsense mutationGiulia Pascolini, Michele Valiante, Silvia Majore, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 13, 2026
Concomitant dominant optic atrophy and juvenile glaucoma in two siblings with a novel OPA1 splicing variantGloria Roberti, Antonio Calabrese, Michele Valiante, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndromeMarco Castori, Michele Valiante, Marco Ritelli, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Elsahy-Waters syndrome: Evidence for autosomal recessive inheritanceMarco Castori, Piero Cascone, Michele Valiante, et al.
Blood Cells, Molecules & Diseases|September 24, 2013
TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern ItalyFrancesca Clementina Radio, Silvia Majore, Francesco Binni, et al.
Psychiatric Genetics|February 7, 2019
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 geneGiulia Pascolini, Silvia Majore, Michele Valiante, et al.
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Showing results (1-10 of 21) with videos related to

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Pageof 3
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|January 26, 2017
Familial melanoma and multiple primary melanomaPaola DE Simone, Michele Valiante, Vitaliano Silipo
European Journal of Medical Genetics|September 3, 2013
Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature reviewMarco Castori, Michele Valiante, Giulia Pascolini, et al.
European Journal of Medical Genetics|June 24, 2020
Answer to Letter to the Editor regarding the article "Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion"Giulia Pascolini, Michele Valiante, Irene Bottillo, et al.
European Journal of Medical Genetics|August 18, 2019
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletionGiulia Pascolini, Michele Valiante, Irene Bottillo, et al.
Minerva Pediatrica|April 14, 2018
Incidental finding of an Xq microdeletion in a girl with trichorhinophalangeal syndrome type I harboring a novel TRPS1 nonsense mutationGiulia Pascolini, Michele Valiante, Silvia Majore, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 13, 2026
Concomitant dominant optic atrophy and juvenile glaucoma in two siblings with a novel OPA1 splicing variantGloria Roberti, Antonio Calabrese, Michele Valiante, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndromeMarco Castori, Michele Valiante, Marco Ritelli, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Elsahy-Waters syndrome: Evidence for autosomal recessive inheritanceMarco Castori, Piero Cascone, Michele Valiante, et al.
Blood Cells, Molecules & Diseases|September 24, 2013
TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern ItalyFrancesca Clementina Radio, Silvia Majore, Francesco Binni, et al.
Psychiatric Genetics|February 7, 2019
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 geneGiulia Pascolini, Silvia Majore, Michele Valiante, et al.
Pageof 3