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S Acierno

Showing results (1-10 of 34) with videos related to

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Journal of Human Genetics|September 15, 2004
Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)Kiyonori Miura, James S Acierno, Stephanie B Seminara
Accident; Analysis and Prevention|June 19, 2004
Vehicle mismatch: injury patterns and severityS Acierno, R Kaufman, F P Rivara, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|September 28, 2010
Surface and wire EMG crosstalk in neighbouring musclesM Solomonow, R Baratta, M Bernardi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
A locus for autosomal recessive idiopathic hypogonadotropic hypogonadism on chromosome 19p13.3James S Acierno, Jenna K Shagoury, Yøusef Bo-Abbas, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|November 1, 1996
The role of vitamin D in normal prostate growth and differentiationB R Konety, G G Schwartz, J S Acierno, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genesYousef Bo-Abbas, James S Acierno, Jenna K Shagoury, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2002
Hypogonadotropic hypogonadism and cerebellar ataxia: detailed phenotypic characterization of a large, extended kindredStephanie B Seminara, James S Acierno, Najim A Abdulwahid, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 geneNelly Pitteloud, James S Acierno, Astrid U Meysing, et al.
Neurology|June 25, 2003
Familial schwannomatosis: exclusion of the NF2 locus as the germline eventM MacCollin, C Willett, B Heinrich, et al.
Endocrine Reviews|January 31, 2019
Clinical Management of Congenital Hypogonadotropic HypogonadismJacques Young, Cheng Xu, Georgios E Papadakis, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Journal of Human Genetics|September 15, 2004
Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)Kiyonori Miura, James S Acierno, Stephanie B Seminara
Accident; Analysis and Prevention|June 19, 2004
Vehicle mismatch: injury patterns and severityS Acierno, R Kaufman, F P Rivara, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|September 28, 2010
Surface and wire EMG crosstalk in neighbouring musclesM Solomonow, R Baratta, M Bernardi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
A locus for autosomal recessive idiopathic hypogonadotropic hypogonadism on chromosome 19p13.3James S Acierno, Jenna K Shagoury, Yøusef Bo-Abbas, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|November 1, 1996
The role of vitamin D in normal prostate growth and differentiationB R Konety, G G Schwartz, J S Acierno, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genesYousef Bo-Abbas, James S Acierno, Jenna K Shagoury, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2002
Hypogonadotropic hypogonadism and cerebellar ataxia: detailed phenotypic characterization of a large, extended kindredStephanie B Seminara, James S Acierno, Najim A Abdulwahid, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 geneNelly Pitteloud, James S Acierno, Astrid U Meysing, et al.
Neurology|June 25, 2003
Familial schwannomatosis: exclusion of the NF2 locus as the germline eventM MacCollin, C Willett, B Heinrich, et al.
Endocrine Reviews|January 31, 2019
Clinical Management of Congenital Hypogonadotropic HypogonadismJacques Young, Cheng Xu, Georgios E Papadakis, et al.
Pageof 4