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G Brunello

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 13, 2021
AMH and AMHR2 Involvement in Congenital Disorders of Sex DevelopmentFranco G Brunello, Rodolfo A Rey
International Journal of Oral and Maxillofacial Surgery|July 19, 2017
The bone lid technique in oral surgery: a case series studyS Sivolella, G Brunello, F Fistarol, et al.
Biochimie|February 8, 2022
MotSASi: Functional short linear motifs (SLiMs) prediction based on genomic single nucleotide variants and structural dataMariano Martín, Franco G Brunello, Carlos P Modenutti, et al.
Journal of the Endocrine Society|September 30, 2021
Diagnosis of Male Central Hypogonadism During ChildhoodRomina P Grinspon, Sebastián Castro, Franco G Brunello, et al.
The American Journal of Pathology|November 14, 2000
Astrocytic alterations in interleukin-6/Soluble interleukin-6 receptor alpha double-transgenic miceA G Brunello, J Weissenberger, A Kappeler, et al.
Biotechnology Advances|April 18, 2016
Powder-based 3D printing for bone tissue engineeringG Brunello, S Sivolella, R Meneghello, et al.
European Journal of Medical Genetics|July 11, 2006
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndromeL Sorasio, G B Ferrero, E Garelli, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[Steinert's myotonic dystrophy: severe neonatal form with unknown family history]P Tonetto, R Spola, R Bagna, et al.
Human Reproduction (Oxford, England)|March 18, 2025
Clinical presentation of congenital hypogonadotropic hypogonadism in males with delayed puberty according to genetic etiology: a systematic review and meta-analysis after reclassification of gene variantsSebastián Castro, Franco G Brunello, Gabriela Sansó, et al.
Human Molecular Genetics|February 27, 2026
Updated compendium of genes and variants associated with congenital hypogonadotropic hypogonadism: systematic review, classification pipeline, and network analysisFranco G Brunello, Sebastián Castro, Jonathan Zaiat, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 13, 2021
AMH and AMHR2 Involvement in Congenital Disorders of Sex DevelopmentFranco G Brunello, Rodolfo A Rey
International Journal of Oral and Maxillofacial Surgery|July 19, 2017
The bone lid technique in oral surgery: a case series studyS Sivolella, G Brunello, F Fistarol, et al.
Biochimie|February 8, 2022
MotSASi: Functional short linear motifs (SLiMs) prediction based on genomic single nucleotide variants and structural dataMariano Martín, Franco G Brunello, Carlos P Modenutti, et al.
Journal of the Endocrine Society|September 30, 2021
Diagnosis of Male Central Hypogonadism During ChildhoodRomina P Grinspon, Sebastián Castro, Franco G Brunello, et al.
The American Journal of Pathology|November 14, 2000
Astrocytic alterations in interleukin-6/Soluble interleukin-6 receptor alpha double-transgenic miceA G Brunello, J Weissenberger, A Kappeler, et al.
Biotechnology Advances|April 18, 2016
Powder-based 3D printing for bone tissue engineeringG Brunello, S Sivolella, R Meneghello, et al.
European Journal of Medical Genetics|July 11, 2006
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndromeL Sorasio, G B Ferrero, E Garelli, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[Steinert's myotonic dystrophy: severe neonatal form with unknown family history]P Tonetto, R Spola, R Bagna, et al.
Human Reproduction (Oxford, England)|March 18, 2025
Clinical presentation of congenital hypogonadotropic hypogonadism in males with delayed puberty according to genetic etiology: a systematic review and meta-analysis after reclassification of gene variantsSebastián Castro, Franco G Brunello, Gabriela Sansó, et al.
Human Molecular Genetics|February 27, 2026
Updated compendium of genes and variants associated with congenital hypogonadotropic hypogonadism: systematic review, classification pipeline, and network analysisFranco G Brunello, Sebastián Castro, Jonathan Zaiat, et al.
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