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au.\*:("MELIS, M. A")

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New case of contiguous gene syndrome at chromosome 8p11.2p12CAU, M; CONGIU, R; ORIGA, R et al.American journal of medical genetics. 2005, Vol 136A, Num 2, pp 221-222, issn 0148-7299, 2 p.Article

Hemoglobin Cagliari (β 60 [E4] VAL → GLU) : a novel unstable thalassemic hemoglobinopathyPODDA, A; GALANELLO, R; MACCIONI, L et al.Blood. 1991, Vol 77, Num 2, pp 371-375, issn 0006-4971, 5 p.Article

Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutationsGALANELLO, R; PAGLIETTI, M. E; ADDIS, M et al.Clinical genetics. 1988, Vol 33, Num 3, pp 151-155, issn 0009-9163Article

Longitudinal study of a newborn with a combination of deletion and nondeletion α-thalassemia-2GALANELLO, R; MELIS, M. A; MACCIONI, M. L et al.Pediatric research. 1984, Vol 18, Num 2, pp 158-162, issn 0031-3998Article

Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathyMUNTONI, F; MELIS, M. A; GANAU, A et al.American journal of human genetics. 1995, Vol 56, Num 1, pp 151-157, issn 0002-9297Article

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene : a European studyVAN ESSEN, A. J; ABBS, S; FERRARI, M et al.Human genetics. 1992, Vol 88, Num 3, pp 249-257, issn 0340-6717Article

Italian experience regarding the prevention of Duchenne and Becker muscular dystrophiesROMEO, G; DEVOTO, M; FELICETTI, L et al.European journal of pediatrics. 1988, Vol 147, Num 4, pp 412-415, issn 0340-6199Article

δ+-Thalassemia in SardiniaPIRASTU, M; GALANELLO, R; MELIS, M. A et al.Blood. 1983, Vol 62, Num 2, pp 341-345, issn 0006-4971Article

Hyperbilirubinaemia in heterozygous β-thalassaemia is related to co-inherited Gilbert's syndromeGALANELLO, R; PERSEU, L; MELIS, M. A et al.British journal of haematology. 1997, Vol 99, Num 2, pp 433-436, issn 0007-1048Article

Identification of a novel T-insertion polymorphism at the DMD locusMUNTONI, F; CAU, M; CONGIU, R et al.Human genetics. 1993, Vol 92, Num 1, issn 0340-6717, p. 103Article

Fetal hydrops in Sardinia : implications for genetic counsellingGALANELLO, R; SANNA, M. A; MACCIONI, L et al.Clinical genetics. 1990, Vol 38, Num 5, pp 327-331, issn 0009-9163Article

Interaction of heterozygous β°-thalassemia with single functional α-globulin geneGALANELLO, R; PAGLIETTI, E; MELIS, M. A et al.American journal of hematology. 1988, Vol 29, Num 2, pp 63-66, issn 0361-8609Article

Phenotype-genotype correlation in haemoglobin H disease in childhoodGALANELLO, R; PIRASTU, M; MELIS, M. A et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 425-429, issn 0022-2593Article

Heterozygous β-thalassemia with thalassemia intermedia phenotypeGASPERINI, D; PERSEU, L; MELIS, M. A et al.American journal of hematology. 1998, Vol 57, Num 1, pp 43-47, issn 0361-8609Article

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathyMUNTONI, F; DI LENARDA, A; MARROSU, M. G et al.Heart (London 1996). 1997, Vol 78, Num 6, pp 608-612, issn 1355-6037Article

Diagnosis of DMD carrier status in a family with No known affected malesMUNTONI, F; MATEDDU, A; CAU, M et al.Developmental medicine and child neurology (Print). 1993, Vol 35, Num 1, pp 70-73, issn 0012-1622Article

Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierMUNTONI, F; MATEDDU, A; MARROSU, M. G et al.Clinical genetics. 1992, Vol 42, Num 1, pp 35-38, issn 0009-9163Article

Molecular analysis of β°-thalassemia intermedia in SardiniaGALANELLO, R; DESSI, E; CAO, A et al.Blood. 1989, Vol 74, Num 2, pp 823-827, issn 0006-4971Article

A family with segregating triplicated alpha globin loci and beta thalassemiaGALANELLO, R; RUGGERI, R; PAGLIETTI, E et al.Blood. 1983, Vol 62, Num 5, pp 1035-1040, issn 0006-4971Article

Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathyMUNTONI, F; CAU, M; MELIS, M. A et al.The New England journal of medicine. 1993, Vol 329, Num 13, pp 921-925, issn 0028-4793Article

Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyMUNTONI, F; MATEDDU, A; CIANCHETTI, C et al.Journal of neurology, neurosurgery and psychiatry. 1993, Vol 56, Num 1, pp 26-31, issn 0022-3050Article

Germinal mosaicism in a Duchenne muscular dystrophy family : implications for genetic counsellingMELIS, M. A; CAU, M; CONGIU, R et al.Clinical genetics. 1993, Vol 43, Num 5, pp 247-249, issn 0009-9163Article

Pharmacology of γ-aminobutyric acidA receptor complex after the in vivo administration of the anxioselective and anticonvulsant β-carboline derivative abecarnilSERRA, M; FODDI, M. C; GHIANI, C. A et al.The Journal of pharmacology and experimental therapeutics. 1992, Vol 263, Num 3, pp 1360-1368, issn 0022-3565Article

Hemoglobin constitution of double heterozygotes for α or β-thalassemia and HB J SardegnaMACCIONI, L; GALANELLO, R; MELIS, M. A et al.Hemoglobin. 1984, Vol 8, Num 5, pp 497-507, issn 0363-0269Article

Phenotypic effect of heterozygous #7B-A and #7B-B°-thalassemia interactionMELIS, M. A; PIRASTU, M; GALANELLO, R et al.Blood. 1983, Vol 62, Num 1, pp 226-229, issn 0006-4971Article

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