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Volatolomics of Sardinian and Spanish Bituminaria : Characterization of Different Accessions Using Chemometrics

Molecules (Basel, Switzerland), 2021-08, Vol.26 (17), p.5247

2021

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The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011)

BioMed research international, 2013-01, Vol.2013, p.739010-8

2013

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The role of institutional investors in enacting stewardship by corporate boards

Corporate governance (Bradford), 2018-07, Vol.18 (4), p.728-747

2018

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Essential Oil Composition of Myrtle (Myrtus communis) Leaves

Journal of herbs, spices & medicinal plants, 2011-01, Vol.17 (1), p.21-34

2011

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Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome

British journal of haematology, 1997-11, Vol.99 (2), p.433-436

1997

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Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy

Heart (British Cardiac Society), 1997-12, Vol.78 (6), p.608-612

1997

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Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy

American journal of human genetics, 1995, Vol.56 (1), p.151-157

1995

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Bio‐agronomic characterization and implications on the potential use as forage of Bituminaria bituminosa and B. morisiana accessions

Grass and forage science, 2018-06, Vol.73 (2), p.284-296

2018

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Human mutation, 2013-09, Vol.34 (9), p.1208-1215

2013

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Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families

European journal of paediatric neurology, 1998, Vol.2 (5), p.255-261

1998

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A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron

Haematologica (Roma), 2008-10, Vol.93 (10), p.1473-1479

2008

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Heterozygous β‐thalassemia with thalassemia intermedia phenotype

American journal of hematology, 1998-01, Vol.57 (1), p.43-47

1998

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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Brain (London, England : 1878), 2014-05, Vol.137 (5), p.1361-1373

2014

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Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy

The New England journal of medicine, 1993-09, Vol.329 (13), p.921-925

1993

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Optimal efficacy of interferon-free HCV retreatment after protease inhibitor failure in real life

Clinical microbiology and infection, 2017-10, Vol.23 (10), p.777.e1-777.e4

2017

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Hemoglobin Cagliari (β 60 [E4] VAL → GLU): A Novel Unstable Thalassemic Hemoglobinopathy

Blood, 1991-01, Vol.77 (2), p.371-375

1991

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X-linked dilated cardiomyopathy and the dystrophin gene

Neuromuscular disorders : NMD, 1999-07, Vol.9 (5), p.339-346

1999

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Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy

Journal of neurology, neurosurgery and psychiatry, 1993-01, Vol.56 (1), p.26-31

1993

Volltextzugriff (PDF)

HCV NS3 sequencing as a reliable and clinically useful tool for the assessment of genotype and resistance mutations for clinical samples with different HCV-RNA levels

Journal of antimicrobial chemotherapy, 2016-03, Vol.71 (3), p.739-750

2016

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Identification of a novel T-insertion polymorphism at the DMD locus

Human genetics, 1993-08, Vol.92 (1), p.103-103

1993

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Results of Membrane-activated Chelator Stroke Intervention Randomized Trial of DP-b99 in Acute Ischemic Stroke

Stroke (1970), 2013-03, Vol.44 (3), p.580-584

2013

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New case of contiguous gene syndrome at chromosome 8p11.2p12

American journal of medical genetics. Part A, 2005-07, Vol.136A (2), p.221-222

2005

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Diagnosis of DMD Carrier Status in a Family with No Known Affected Males

Developmental medicine and child neurology, 1993-01, Vol.35 (1), p.70-73

1993

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Volatolomics of Sardinian and Spanish Bituminaria : Characterization of Different Accessions Using Chemometrics

The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011)

The role of institutional investors in enacting stewardship by corporate boards

Essential Oil Composition of Myrtle (Myrtus communis) Leaves

Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy

Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy

Bio‐agronomic characterization and implications on the potential use as forage of Bituminaria bituminosa and B. morisiana accessions

Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: I: Fetal risks

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: II: Maternal risks

Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families

A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron

Heterozygous β‐thalassemia with thalassemia intermedia phenotype

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy

Optimal efficacy of interferon-free HCV retreatment after protease inhibitor failure in real life

Hemoglobin Cagliari (β 60 [E4] VAL → GLU): A Novel Unstable Thalassemic Hemoglobinopathy

X-linked dilated cardiomyopathy and the dystrophin gene

Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy

HCV NS3 sequencing as a reliable and clinically useful tool for the assessment of genotype and resistance mutations for clinical samples with different HCV-RNA levels

Identification of a novel T-insertion polymorphism at the DMD locus

Results of Membrane-activated Chelator Stroke Intervention Randomized Trial of DP-b99 in Acute Ischemic Stroke

New case of contiguous gene syndrome at chromosome 8p11.2p12

Diagnosis of DMD Carrier Status in a Family with No Known Affected Males

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