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Soledad Kleppe

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Current Treatment Options in Neurology|June 7, 2003
Urea Cycle DisordersSoledad Kleppe, Asad Mian, Brendan Lee
Archivos Argentinos De Pediatria|October 30, 2023
Monochorionic twin pregnancy from the perspective of the theory of complexityCésar Meller, Soledad Kleppe, Horacio Aiello, et al.
Genes|February 24, 2024
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin AmericaMaria Agustina De Rosa, Maria T Bernardi, Soledad Kleppe, et al.
JCEM Case Reports|May 7, 2026
Infertility as a possible diagnostic feature of Carney complexPablo Knoblovits, Erika Abelleira, Gastón Rey Valzacchi, et al.
Archivos Argentinos De Pediatria|October 26, 2022
Initial management of acute hyperammonemia in pediatricsHernán Eiroa, Consuelo Durand, Marina Szlago, et al.
The Journal of Nutrition|October 7, 2004
Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolismFernando Scaglia, Nicola Brunetti-Pierri, Soledad Kleppe, et al.
Human Genetics|July 16, 2005
Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthaseSilke Leimkühler, Mathilde Charcosset, Philippe Latour, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 27, 2026
Apolipoprotein L1 (APOL1) and NephropathyAlanis Yael Szyferman, Soledad Kleppe, Fabrizio Cristiano, et al.
The Journal of Pediatrics|March 27, 2007
Ethical and legal implications of genetic testing in androgen insensitivity syndromeJonathan S Berg, Shannon L French, Laurence B McCullough, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 1, 2004
Long-term correction of ornithine transcarbamylase deficiency by WPRE-mediated overexpression using a helper-dependent adenovirusAsad Mian, W Michael McCormack, Viraj Mane, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Current Treatment Options in Neurology|June 7, 2003
Urea Cycle DisordersSoledad Kleppe, Asad Mian, Brendan Lee
Archivos Argentinos De Pediatria|October 30, 2023
Monochorionic twin pregnancy from the perspective of the theory of complexityCésar Meller, Soledad Kleppe, Horacio Aiello, et al.
Genes|February 24, 2024
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin AmericaMaria Agustina De Rosa, Maria T Bernardi, Soledad Kleppe, et al.
JCEM Case Reports|May 7, 2026
Infertility as a possible diagnostic feature of Carney complexPablo Knoblovits, Erika Abelleira, Gastón Rey Valzacchi, et al.
Archivos Argentinos De Pediatria|October 26, 2022
Initial management of acute hyperammonemia in pediatricsHernán Eiroa, Consuelo Durand, Marina Szlago, et al.
The Journal of Nutrition|October 7, 2004
Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolismFernando Scaglia, Nicola Brunetti-Pierri, Soledad Kleppe, et al.
Human Genetics|July 16, 2005
Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthaseSilke Leimkühler, Mathilde Charcosset, Philippe Latour, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 27, 2026
Apolipoprotein L1 (APOL1) and NephropathyAlanis Yael Szyferman, Soledad Kleppe, Fabrizio Cristiano, et al.
The Journal of Pediatrics|March 27, 2007
Ethical and legal implications of genetic testing in androgen insensitivity syndromeJonathan S Berg, Shannon L French, Laurence B McCullough, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 1, 2004
Long-term correction of ornithine transcarbamylase deficiency by WPRE-mediated overexpression using a helper-dependent adenovirusAsad Mian, W Michael McCormack, Viraj Mane, et al.
Pageof 2