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Vito Guarnieri

Showing results (51-60 of 79) with videos related to

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Endocrine|June 17, 2011
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian familySandra Mastroianno, Massimo Torlontano, Alfredo Scillitani, et al.
Endocrine|November 28, 2024
Aberrant promoter methylation, expression and function of RASSF1A gene in a series of Italian parathyroid tumorsChiara Verdelli, Federico Pio Fabrizio, Paola Maroni, et al.
Molecular Genetics and Metabolism|July 14, 2012
CASR gene activating mutations in two families with autosomal dominant hypocalcemiaVito Guarnieri, Angela Valentina D'Elia, Filomena Baorda, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2006
HOXA1 gene variants influence head growth rates in humansLucia Anna Muscarella, Vito Guarnieri, Roberto Sacco, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 2010
Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three yearsVito Guarnieri, Lucie Canaff, Francisco H J Yun, et al.
Molecular Autism|August 4, 2010
Candidate gene study of HOXB1 in autism spectrum disorderLucia A Muscarella, Vito Guarnieri, Roberto Sacco, et al.
Endocrine Connections|November 4, 2017
<i>MEN1</i> gene mutation with parathyroid carcinoma: first report of a familial caseLuigia Cinque, Angelo Sparaneo, Antonio S Salcuni, et al.
European Journal of Endocrinology|June 27, 2014
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidismCristina Eller-Vainicher, Claudia Battista, Vito Guarnieri, et al.
European Journal of Endocrinology|January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disordersLucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
Human Mutation|August 31, 2018
A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletionGrazia Nardella, Grazia Visci, Vito Guarnieri, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Endocrine|June 17, 2011
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian familySandra Mastroianno, Massimo Torlontano, Alfredo Scillitani, et al.
Endocrine|November 28, 2024
Aberrant promoter methylation, expression and function of RASSF1A gene in a series of Italian parathyroid tumorsChiara Verdelli, Federico Pio Fabrizio, Paola Maroni, et al.
Molecular Genetics and Metabolism|July 14, 2012
CASR gene activating mutations in two families with autosomal dominant hypocalcemiaVito Guarnieri, Angela Valentina D'Elia, Filomena Baorda, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2006
HOXA1 gene variants influence head growth rates in humansLucia Anna Muscarella, Vito Guarnieri, Roberto Sacco, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 2010
Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three yearsVito Guarnieri, Lucie Canaff, Francisco H J Yun, et al.
Molecular Autism|August 4, 2010
Candidate gene study of HOXB1 in autism spectrum disorderLucia A Muscarella, Vito Guarnieri, Roberto Sacco, et al.
Endocrine Connections|November 4, 2017
<i>MEN1</i> gene mutation with parathyroid carcinoma: first report of a familial caseLuigia Cinque, Angelo Sparaneo, Antonio S Salcuni, et al.
European Journal of Endocrinology|June 27, 2014
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidismCristina Eller-Vainicher, Claudia Battista, Vito Guarnieri, et al.
European Journal of Endocrinology|January 17, 2022
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disordersLucie Canaff, Vito Guarnieri, Yoojung Kim, et al.
Human Mutation|August 31, 2018
A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletionGrazia Nardella, Grazia Visci, Vito Guarnieri, et al.
Pageof 8