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M A Melis

Showing results (41-50 of 58) with videos related to

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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.
British Journal of Haematology|December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndromeR Galanello, L Perseu, M A Melis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
The Year in Immunology|January 1, 1993
Rearrangement of immunoglobin heavy chain constant region in Italian populationU Cariota, A Brusco, C Boccazzi, et al.
Acta Haematologica|January 1, 1992
HbH disease in Sardinia: molecular, hematological and clinical aspectsR Galanello, B Aru, C Dessì, et al.
European Journal of Pediatrics|May 1, 1988
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophiesG Romeo, M Devoto, N Archidiacono, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
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.
British Journal of Haematology|December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndromeR Galanello, L Perseu, M A Melis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
The Year in Immunology|January 1, 1993
Rearrangement of immunoglobin heavy chain constant region in Italian populationU Cariota, A Brusco, C Boccazzi, et al.
Acta Haematologica|January 1, 1992
HbH disease in Sardinia: molecular, hematological and clinical aspectsR Galanello, B Aru, C Dessì, et al.
European Journal of Pediatrics|May 1, 1988
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophiesG Romeo, M Devoto, N Archidiacono, et al.
Pageof 6