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Paola De Filippi

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International Journal of Paediatric Dentistry|May 1, 2008
Deletion of PAX9 and oligodontia: a third family and review of the literatureAndrea Guala, Vittorio Falco, Guido Breedveld, et al.
Journal of Inherited Metabolic Disease|June 21, 2006
Dietary treatment in adult-onset type II glycogenosisSabrina Ravaglia, Anna Pichiecchio, Miriam Rossi, et al.
Molecular Genetics and Metabolism|June 19, 2012
Can genes influencing muscle function affect the therapeutic response to enzyme replacement therapy (ERT) in late-onset type II glycogenosis?Sabrina Ravaglia, Paola De Filippi, Anna Pichiecchio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2010
The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe diseasePaola de Filippi, Sabrina Ravaglia, Bruno Bembi, et al.
Oncotarget|March 17, 2016
Mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia: a report from the Italian AIEOP study groupSilvia Bresolin, Paola De Filippi, Francesca Vendemini, et al.
Cancer Genetics and Cytogenetics|January 22, 2004
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effectsEmanuela Maserati, Antonella Minelli, Giuseppe Menna, et al.
British Journal of Haematology|September 25, 2009
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemiaPaola De Filippi, Marco Zecca, Daniela Lisini, et al.
Pediatric Research|November 25, 2003
Abnormal cell surface antigen expression in individuals with variant CD45 splicing and histiocytosisSally Boxall, James McCormick, Peter Beverley, et al.
Pediatric Blood & Cancer|December 21, 2011
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemiaPaola De Filippi, Marco Zecca, Francesca Novara, et al.
British Journal of Haematology|February 21, 2006
Specific polymorphisms of cytokine genes are associated with different risks to develop single-system or multi-system childhood Langerhans cell histiocytosisPaola De Filippi, Carla Badulli, Mariaclara Cuccia, et al.
Pageof 2

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

Sort By:
Pageof 2
International Journal of Paediatric Dentistry|May 1, 2008
Deletion of PAX9 and oligodontia: a third family and review of the literatureAndrea Guala, Vittorio Falco, Guido Breedveld, et al.
Journal of Inherited Metabolic Disease|June 21, 2006
Dietary treatment in adult-onset type II glycogenosisSabrina Ravaglia, Anna Pichiecchio, Miriam Rossi, et al.
Molecular Genetics and Metabolism|June 19, 2012
Can genes influencing muscle function affect the therapeutic response to enzyme replacement therapy (ERT) in late-onset type II glycogenosis?Sabrina Ravaglia, Paola De Filippi, Anna Pichiecchio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2010
The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe diseasePaola de Filippi, Sabrina Ravaglia, Bruno Bembi, et al.
Oncotarget|March 17, 2016
Mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia: a report from the Italian AIEOP study groupSilvia Bresolin, Paola De Filippi, Francesca Vendemini, et al.
Cancer Genetics and Cytogenetics|January 22, 2004
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effectsEmanuela Maserati, Antonella Minelli, Giuseppe Menna, et al.
British Journal of Haematology|September 25, 2009
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemiaPaola De Filippi, Marco Zecca, Daniela Lisini, et al.
Pediatric Research|November 25, 2003
Abnormal cell surface antigen expression in individuals with variant CD45 splicing and histiocytosisSally Boxall, James McCormick, Peter Beverley, et al.
Pediatric Blood & Cancer|December 21, 2011
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemiaPaola De Filippi, Marco Zecca, Francesca Novara, et al.
British Journal of Haematology|February 21, 2006
Specific polymorphisms of cytokine genes are associated with different risks to develop single-system or multi-system childhood Langerhans cell histiocytosisPaola De Filippi, Carla Badulli, Mariaclara Cuccia, et al.
Pageof 2