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A Ponzone

Showing results (21-30 of 89) with videos related to

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La Nouvelle Presse Medicale|September 15, 1973
[Fluorescence and non-disjonction]H P Franceschini, C Fabris, A Ponzone
Journal of Inherited Metabolic Disease|January 1, 1985
Differential diagnosis of tetrahydrobiopterin deficiencyA Niederwieser, A Ponzone, H C Curtius
Minerva Pediatrica|May 26, 1975
[Blastic transformation of lymphocytes of newborn infants produced with human lymphoreticular RNA]M Fazio, C Bachi, P Nicola, et al.
Minerva Pediatrica|January 7, 1971
[Agammaglobulinemia with transitory recurrent agranulocytosis]N Svilokos, C Fabris, G Ciriotti, et al.
The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.
Minerva Pediatrica|September 1, 1971
[Importance of omphaloportography in the newborn]D Pavesio, A Balocco, A Ponzone, et al.
American Journal of Medical Genetics|May 14, 1999
Goldenhar anomaly in one of triplets derived from in vitro fertilizationS Ferraris, M Silengo, A Ponzone, et al.
Acta Paediatrica Scandinavica|May 1, 1973
Sex chromosome anomalies detection and fluorescenceC Fabris, P Franceschini, G Bogetti, et al.
Pediatrie|January 1, 1987
[Trial of indirect screening of tetrahydrobiopterin deficiency]S Ferraris, O Guardamagna, G Bracco, et al.
Acta Neurologica|July 1, 1974
[Clinico-anatomical studies in a case of spongious encephalopathy of the van Bogaert-Bertrand type]D Schiffer, R Torta, T Gaino, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
La Nouvelle Presse Medicale|September 15, 1973
[Fluorescence and non-disjonction]H P Franceschini, C Fabris, A Ponzone
Journal of Inherited Metabolic Disease|January 1, 1985
Differential diagnosis of tetrahydrobiopterin deficiencyA Niederwieser, A Ponzone, H C Curtius
Minerva Pediatrica|May 26, 1975
[Blastic transformation of lymphocytes of newborn infants produced with human lymphoreticular RNA]M Fazio, C Bachi, P Nicola, et al.
Minerva Pediatrica|January 7, 1971
[Agammaglobulinemia with transitory recurrent agranulocytosis]N Svilokos, C Fabris, G Ciriotti, et al.
The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.
Minerva Pediatrica|September 1, 1971
[Importance of omphaloportography in the newborn]D Pavesio, A Balocco, A Ponzone, et al.
American Journal of Medical Genetics|May 14, 1999
Goldenhar anomaly in one of triplets derived from in vitro fertilizationS Ferraris, M Silengo, A Ponzone, et al.
Acta Paediatrica Scandinavica|May 1, 1973
Sex chromosome anomalies detection and fluorescenceC Fabris, P Franceschini, G Bogetti, et al.
Pediatrie|January 1, 1987
[Trial of indirect screening of tetrahydrobiopterin deficiency]S Ferraris, O Guardamagna, G Bracco, et al.
Acta Neurologica|July 1, 1974
[Clinico-anatomical studies in a case of spongious encephalopathy of the van Bogaert-Bertrand type]D Schiffer, R Torta, T Gaino, et al.
Pageof 9