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A Melis

Showing results (141-150 of 171) with videos related to

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British Journal of Haematology|August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemiaR Galanello, S Barella, L Maccioni, et al.
Experimental and Molecular Pathology|December 24, 2008
High frequencies of short alleles of NOS1 (CA)n polymorphism in beta(0)39 carriers from Corsica Island (France)I S Piras, A Falchi, A Melis, et al.
Clinical Genetics|July 1, 1992
Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierF Muntoni, A Mateddu, M G Marrosu, et al.
American Journal of Hematology|January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotypeD Gasperini, L Perseu, M A Melis, et al.
Journal of Medical Virology|December 1, 1993
Markers of hepatitis C virus infection in Sardinian blood donors: relationship with alanine aminotransferase levelsM E Lai, A P Mazzoleni, P Farci, et al.
Clinical Genetics|November 1, 1990
Fetal hydrops in Sardinia: implications for genetic counsellingR Galanello, M A Sanna, L Maccioni, et al.
Human Mutation|February 6, 1998
Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathyM A Melis, F Muntoni, M Cau, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1992
Pharmacology of gamma-aminobutyric acidA receptor complex after the in vivo administration of the anxioselective and anticonvulsant beta-carboline derivative abecarnilM Serra, M C Foddi, C A Ghiani, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.
Blood|April 15, 1990
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosomeR Galanello, M A Melis, A Podda, et al.
Pageof 18

Showing results (141-150 of 171) with videos related to

Sort By:
Pageof 18
British Journal of Haematology|August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemiaR Galanello, S Barella, L Maccioni, et al.
Experimental and Molecular Pathology|December 24, 2008
High frequencies of short alleles of NOS1 (CA)n polymorphism in beta(0)39 carriers from Corsica Island (France)I S Piras, A Falchi, A Melis, et al.
Clinical Genetics|July 1, 1992
Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierF Muntoni, A Mateddu, M G Marrosu, et al.
American Journal of Hematology|January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotypeD Gasperini, L Perseu, M A Melis, et al.
Journal of Medical Virology|December 1, 1993
Markers of hepatitis C virus infection in Sardinian blood donors: relationship with alanine aminotransferase levelsM E Lai, A P Mazzoleni, P Farci, et al.
Clinical Genetics|November 1, 1990
Fetal hydrops in Sardinia: implications for genetic counsellingR Galanello, M A Sanna, L Maccioni, et al.
Human Mutation|February 6, 1998
Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathyM A Melis, F Muntoni, M Cau, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1992
Pharmacology of gamma-aminobutyric acidA receptor complex after the in vivo administration of the anxioselective and anticonvulsant beta-carboline derivative abecarnilM Serra, M C Foddi, C A Ghiani, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.
Blood|April 15, 1990
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosomeR Galanello, M A Melis, A Podda, et al.
Pageof 18