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G Loudianos

Showing results (11-20 of 23) with videos related to

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Blood|January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin geneP Moi, G Loudianos, J Lavinha, et al.
Italian Journal of Gastroenterology and Hepatology|October 6, 1998
Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected membersM Merli, M Patriarca, G Loudianos, et al.
Blood|March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutationsS Murru, G Loudianos, M Deiana, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Molecular analysis of atypical beta-thalassemia heterozygotesM Pirastu, M S Ristaldi, G Loudianos, et al.
Human Genetics|December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patientsG Loudianos, V Dessì, A Angius, et al.
Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.
Journal of Medical Genetics|April 1, 1990
Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNAM C Rosatelli, R Sardu, T Tuveri, et al.
Prenatal Diagnosis|October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markersG Loudianos, A L Figus, A Loi, et al.
British Journal of Haematology|April 1, 1990
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian populationM S Ristaldi, S Murru, G Loudianos, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Haplotype and mutation analysis in Greek patients with Wilson diseaseG Loudianos, V Dessì, M Lovicu, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Blood|January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin geneP Moi, G Loudianos, J Lavinha, et al.
Italian Journal of Gastroenterology and Hepatology|October 6, 1998
Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected membersM Merli, M Patriarca, G Loudianos, et al.
Blood|March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutationsS Murru, G Loudianos, M Deiana, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Molecular analysis of atypical beta-thalassemia heterozygotesM Pirastu, M S Ristaldi, G Loudianos, et al.
Human Genetics|December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patientsG Loudianos, V Dessì, A Angius, et al.
Prilozi|January 31, 2012
Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case ReportZ S Gucev, N Pop-Jordanova, V Calovska, et al.
Journal of Medical Genetics|April 1, 1990
Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNAM C Rosatelli, R Sardu, T Tuveri, et al.
Prenatal Diagnosis|October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markersG Loudianos, A L Figus, A Loi, et al.
British Journal of Haematology|April 1, 1990
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian populationM S Ristaldi, S Murru, G Loudianos, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Haplotype and mutation analysis in Greek patients with Wilson diseaseG Loudianos, V Dessì, M Lovicu, et al.
Pageof 3