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Daniela Antuzzi

Showing results (11-20 of 27) with videos related to

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Case Reports in Gastroenterology|September 8, 2011
Splenomegaly as a primary manifestation of Gaucher disease in a young adult womanGiuseppe Merra, Antonio Dal Lago, Roberta Ricci, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 15, 2016
Extensive irregular Mongolian blue spots as a clue for GM1 gangliosidosis type 1Giulia Bersani, Cristina Guerriero, Francesco Ricci, et al.
European Journal of Case Reports in Internal Medicine|February 14, 2019
Anderson-Fabry's Disease: A Rare but Treatable Case of Fever of Unknown OriginFrancesca Graziani, Aureliano Ruggio, Antonio Iaconelli, et al.
Annals of Emergency Medicine|January 7, 2003
Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic comaRita Gaspari, Andrea Arcangeli, Sonia Mensi, et al.
Human Pathology|March 13, 2012
Cardiac and skeletal myopathy in Fabry disease: a clinicopathologic correlative studyCristina Chimenti, Luca Padua, Costanza Pazzaglia, et al.
Circulation|August 18, 2004
Prevalence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathyCristina Chimenti, Maurizio Pieroni, Emanuela Morgante, et al.
European Journal of Internal Medicine|April 17, 2016
The impact of fever/hyperthermia in the diagnosis of Fabry: A retrospective analysisElena Verrecchia, Anna Zampetti, Daniela Antuzzi, et al.
Journal of Clinical Medicine|November 27, 2021
The Use of Chitotriosidase as a Marker of Active Sarcoidosis and in the Diagnosis of Fever of Unknown Origin (FUO)Angela Maria Di Francesco, Elena Verrecchia, Ludovico Luca Sicignano, et al.
Cytokine|January 22, 2013
Vascular endothelial growth factor (VEGF-a) in Fabry disease: association with cutaneous and systemic manifestations with vascular involvementAnna Zampetti, Maria Gnarra, Walter Borsini, et al.
Human Mutation|February 16, 2005
Identification and characterization of five novel MAN2B1 mutations in Italian patients with alpha-mannosidosisMichele Sbaragli, Lucia Bibi, Maria Gabriela Pittis, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Case Reports in Gastroenterology|September 8, 2011
Splenomegaly as a primary manifestation of Gaucher disease in a young adult womanGiuseppe Merra, Antonio Dal Lago, Roberta Ricci, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|January 15, 2016
Extensive irregular Mongolian blue spots as a clue for GM1 gangliosidosis type 1Giulia Bersani, Cristina Guerriero, Francesco Ricci, et al.
European Journal of Case Reports in Internal Medicine|February 14, 2019
Anderson-Fabry's Disease: A Rare but Treatable Case of Fever of Unknown OriginFrancesca Graziani, Aureliano Ruggio, Antonio Iaconelli, et al.
Annals of Emergency Medicine|January 7, 2003
Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic comaRita Gaspari, Andrea Arcangeli, Sonia Mensi, et al.
Human Pathology|March 13, 2012
Cardiac and skeletal myopathy in Fabry disease: a clinicopathologic correlative studyCristina Chimenti, Luca Padua, Costanza Pazzaglia, et al.
Circulation|August 18, 2004
Prevalence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathyCristina Chimenti, Maurizio Pieroni, Emanuela Morgante, et al.
European Journal of Internal Medicine|April 17, 2016
The impact of fever/hyperthermia in the diagnosis of Fabry: A retrospective analysisElena Verrecchia, Anna Zampetti, Daniela Antuzzi, et al.
Journal of Clinical Medicine|November 27, 2021
The Use of Chitotriosidase as a Marker of Active Sarcoidosis and in the Diagnosis of Fever of Unknown Origin (FUO)Angela Maria Di Francesco, Elena Verrecchia, Ludovico Luca Sicignano, et al.
Cytokine|January 22, 2013
Vascular endothelial growth factor (VEGF-a) in Fabry disease: association with cutaneous and systemic manifestations with vascular involvementAnna Zampetti, Maria Gnarra, Walter Borsini, et al.
Human Mutation|February 16, 2005
Identification and characterization of five novel MAN2B1 mutations in Italian patients with alpha-mannosidosisMichele Sbaragli, Lucia Bibi, Maria Gabriela Pittis, et al.
Pageof 3