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F De Luca

Showing results (41-50 of 350) with videos related to

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Rassegna Internazionale Di Clinica E Terapia|November 30, 1971
[Splenic rupture in a patient with Gaucher's disease]R A Schettino, F De Luca, V Sgambati
Molecular Genetics and Metabolism|August 28, 1998
Activating mutations of the Ca2+-sensing receptorE E Mancilla, F De Luca, J Baron
Gene|July 22, 1991
Mitochondrial DNA in the sea urchin Arbacia lixula: nucleotide sequence differences between two polymorphic molecules indicate asymmetry of mutationsC De Giorgi, F De Luca, C Saccone
Helvetica Paediatrica Acta|June 1, 1987
Obesity in a child with untreated coeliac diseaseS Conti Nibali, G Magazzù, F De Luca
Rassegna Internazionale Di Clinica E Terapia|September 15, 1971
[On a case of acute spontaneous chyloperitoneum]G Ruiz, R A Schettino, F De Luca
Minerva Pediatrica|April 30, 1981
[Clinical findings during a 3-year experience in screening newborn infants for congenital hypothyroidism]G Lombardo, F De Luca, M Gemelli, et al.
Acta Paediatrica Scandinavica|January 1, 1986
Hyperfunctioning thyroid nodules in children and adolescentsF de Luca, J L Chaussain, J C Job
Magnetic Resonance in Medicine|January 1, 1987
Maximum entropy method in phase-encoding NMR imagingB C De Simone, F De Luca, B Maraviglia
Histopathology|May 1, 1977
Morphological aspects of the endocrine pancreas in a prednisolone-treated infantG Barresi, C Inferrera, M Gemelli, et al.
Acta Neurologica|June 1, 1983
Myelographic features of redundant nerve roots of the cauda equinaA Gambardella, S Sorrentino, S Meoli, et al.
Pageof 35

Showing results (41-50 of 350) with videos related to

Sort By:
Pageof 35
Rassegna Internazionale Di Clinica E Terapia|November 30, 1971
[Splenic rupture in a patient with Gaucher's disease]R A Schettino, F De Luca, V Sgambati
Molecular Genetics and Metabolism|August 28, 1998
Activating mutations of the Ca2+-sensing receptorE E Mancilla, F De Luca, J Baron
Gene|July 22, 1991
Mitochondrial DNA in the sea urchin Arbacia lixula: nucleotide sequence differences between two polymorphic molecules indicate asymmetry of mutationsC De Giorgi, F De Luca, C Saccone
Helvetica Paediatrica Acta|June 1, 1987
Obesity in a child with untreated coeliac diseaseS Conti Nibali, G Magazzù, F De Luca
Rassegna Internazionale Di Clinica E Terapia|September 15, 1971
[On a case of acute spontaneous chyloperitoneum]G Ruiz, R A Schettino, F De Luca
Minerva Pediatrica|April 30, 1981
[Clinical findings during a 3-year experience in screening newborn infants for congenital hypothyroidism]G Lombardo, F De Luca, M Gemelli, et al.
Acta Paediatrica Scandinavica|January 1, 1986
Hyperfunctioning thyroid nodules in children and adolescentsF de Luca, J L Chaussain, J C Job
Magnetic Resonance in Medicine|January 1, 1987
Maximum entropy method in phase-encoding NMR imagingB C De Simone, F De Luca, B Maraviglia
Histopathology|May 1, 1977
Morphological aspects of the endocrine pancreas in a prednisolone-treated infantG Barresi, C Inferrera, M Gemelli, et al.
Acta Neurologica|June 1, 1983
Myelographic features of redundant nerve roots of the cauda equinaA Gambardella, S Sorrentino, S Meoli, et al.
Pageof 35