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Fulvia Baldinotti

Showing results (1-10 of 35) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 20, 2019
Paternity in 5α-Reductase-2 Deficiency: Report of Two Brothers with Spontaneous or Assisted Fertility and Literature ReviewSilvano Bertelloni, Fulvia Baldinotti, Giampiero I Baroncelli, et al.
Frontiers in Endocrinology|May 1, 2024
Gonadal dysfunction in a man with Noonan syndrome from the <i>LZTR1</i> variant: case report and review of literatureFrancesca Orsolini, Luisa Pignata, Fulvia Baldinotti, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominantAntonella Fogli, Roberta Battini, Fulvia Baldinotti, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominantAntonella Fogli, Roberta Battini, Fulvia Baldinotti, et al.
Fertility and Sterility|May 12, 2004
Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic manAngelo Valetto, Veronica Bertini, Erika Rapalini, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 30, 2004
Premature ovarian failure and fragile X premutation: a study on 45 womenCecilia Bussani, Laura Papi, Roberta Sestini, et al.
Hormones (Athens, Greece)|April 30, 2013
IGF-I generation test in prepubertal children with Noonan syndrome due to mutations in the PTPN11 geneSilvano Bertelloni, Giampiero I Baroncelli, Eleonora Dati, et al.
Analytical Biochemistry|July 13, 2004
HPLC assay for guanidinoacetate methyltransferaseMaria Grazia Alessandrì, Lisa Celati, Roberta Battini, et al.
American Journal of Physical Medicine & Rehabilitation|September 26, 2003
Electrodiagnostic evidence of phrenic nerve demyelination in Charcot-Marie-Tooth disease 1ALaura Sagliocco, Giovanni Orlandi, Rosa Calabrese, et al.
American Journal of Medical Genetics|January 25, 2002
Response to local dihydrotestosterone treatment in a patient with partial androgen-insensitivity syndrome due to a novel mutation in the androgen receptor geneCarlo Foresta, Andrea Bettella, Alberto Ferlin, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 20, 2019
Paternity in 5α-Reductase-2 Deficiency: Report of Two Brothers with Spontaneous or Assisted Fertility and Literature ReviewSilvano Bertelloni, Fulvia Baldinotti, Giampiero I Baroncelli, et al.
Frontiers in Endocrinology|May 1, 2024
Gonadal dysfunction in a man with Noonan syndrome from the <i>LZTR1</i> variant: case report and review of literatureFrancesca Orsolini, Luisa Pignata, Fulvia Baldinotti, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominantAntonella Fogli, Roberta Battini, Fulvia Baldinotti, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominantAntonella Fogli, Roberta Battini, Fulvia Baldinotti, et al.
Fertility and Sterility|May 12, 2004
Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic manAngelo Valetto, Veronica Bertini, Erika Rapalini, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 30, 2004
Premature ovarian failure and fragile X premutation: a study on 45 womenCecilia Bussani, Laura Papi, Roberta Sestini, et al.
Hormones (Athens, Greece)|April 30, 2013
IGF-I generation test in prepubertal children with Noonan syndrome due to mutations in the PTPN11 geneSilvano Bertelloni, Giampiero I Baroncelli, Eleonora Dati, et al.
Analytical Biochemistry|July 13, 2004
HPLC assay for guanidinoacetate methyltransferaseMaria Grazia Alessandrì, Lisa Celati, Roberta Battini, et al.
American Journal of Physical Medicine & Rehabilitation|September 26, 2003
Electrodiagnostic evidence of phrenic nerve demyelination in Charcot-Marie-Tooth disease 1ALaura Sagliocco, Giovanni Orlandi, Rosa Calabrese, et al.
American Journal of Medical Genetics|January 25, 2002
Response to local dihydrotestosterone treatment in a patient with partial androgen-insensitivity syndrome due to a novel mutation in the androgen receptor geneCarlo Foresta, Andrea Bettella, Alberto Ferlin, et al.
Pageof 4