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B Colombo

Showing results (191-200 of 243) with videos related to

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British Journal of Haematology|March 1, 1993
Iron status in red cell pyruvate kinase deficiency: study of Italian casesA Zanella, A Berzuini, M B Colombo, et al.
Biochimica Et Biophysica Acta|September 27, 1977
Chemical characterization of a new haemoglobin variant haemoglobin J Cubujuqui (alpha2141(HC3)Arg replaced by Ser beta2)G F Sáenz, J Elizondo, M A Alvarado, et al.
Neurology|February 20, 1999
Comparison of MS clinical phenotypes using conventional and magnetization transfer MRIM Filippi, G Iannucci, C Tortorella, et al.
Haematologica|May 1, 1988
The molecular heterogeneity of chronic lymphocytic leukemia: further dataG Martinez, R Ferreira, A Hernandez, et al.
British Journal of Rheumatology|December 1, 1991
Immunoglobulin heavy chain gene polymorphisms in Italian patients with psoriasis and psoriatic arthritisL I Sakkas, A Marchesoni, L A Kerr, et al.
Sangre|June 1, 1988
[Prenatal diagnosis of carriers of hemophilia B in a Cuban family using DNA analysis]A Hernández, G Martínez, L Corral, et al.
International Journal of Immunopathology and Pharmacology|October 4, 2008
Consequences of long-lasting persistent allergic rhinitis in adolescentsG L Marseglia, M Grignani, P Civallero, et al.
American Journal of Human Genetics|November 1, 1986
Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypesA Di Rienzo, A Novelletto, M C Aliquò, et al.
Journal of Neurology|August 1, 1995
Acute myelopathy of unknown aetiology: a clinical, neurophysiological and MRI study of short- and long-term prognostic factorsV Martinelli, G Comi, M Rovaris, et al.
Acta Neurologica Scandinavica|September 1, 1991
Paraclinical tests in acute-onset optic neuritis: basal data and results of a short follow-upV Martinelli, G Comi, M Filippi, et al.
Pageof 25

Showing results (191-200 of 243) with videos related to

Sort By:
Pageof 25
British Journal of Haematology|March 1, 1993
Iron status in red cell pyruvate kinase deficiency: study of Italian casesA Zanella, A Berzuini, M B Colombo, et al.
Biochimica Et Biophysica Acta|September 27, 1977
Chemical characterization of a new haemoglobin variant haemoglobin J Cubujuqui (alpha2141(HC3)Arg replaced by Ser beta2)G F Sáenz, J Elizondo, M A Alvarado, et al.
Neurology|February 20, 1999
Comparison of MS clinical phenotypes using conventional and magnetization transfer MRIM Filippi, G Iannucci, C Tortorella, et al.
Haematologica|May 1, 1988
The molecular heterogeneity of chronic lymphocytic leukemia: further dataG Martinez, R Ferreira, A Hernandez, et al.
British Journal of Rheumatology|December 1, 1991
Immunoglobulin heavy chain gene polymorphisms in Italian patients with psoriasis and psoriatic arthritisL I Sakkas, A Marchesoni, L A Kerr, et al.
Sangre|June 1, 1988
[Prenatal diagnosis of carriers of hemophilia B in a Cuban family using DNA analysis]A Hernández, G Martínez, L Corral, et al.
International Journal of Immunopathology and Pharmacology|October 4, 2008
Consequences of long-lasting persistent allergic rhinitis in adolescentsG L Marseglia, M Grignani, P Civallero, et al.
American Journal of Human Genetics|November 1, 1986
Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypesA Di Rienzo, A Novelletto, M C Aliquò, et al.
Journal of Neurology|August 1, 1995
Acute myelopathy of unknown aetiology: a clinical, neurophysiological and MRI study of short- and long-term prognostic factorsV Martinelli, G Comi, M Rovaris, et al.
Acta Neurologica Scandinavica|September 1, 1991
Paraclinical tests in acute-onset optic neuritis: basal data and results of a short follow-upV Martinelli, G Comi, M Filippi, et al.
Pageof 25