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Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for IKs

British journal of pharmacology, 2010-01, Vol.159 (1), p.93-101

2010

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Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for I Ks

British journal of pharmacology, 2010-01, Vol.159 (1), p.93-101

2010

Volltextzugriff (PDF)

Dexrazoxane protects the heart from acute doxorubicin-induced QT prolongation: a key role for IKs : QT Safety

British journal of pharmacology, 2010, Vol.159 (1), p.93-101

2010

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Electrophysiological effects of azimilide in an in vitro model of simulated-ischemia and reperfusion in guinea-pig ventricular myocardium

European journal of pharmacology, 2005-08, Vol.518 (2-3), p.165-174

2005

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Pont Vasco de Gama : les fondations maritimes

Travaux (Paris), 1998 (743), p.33-41

1998

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Sensitivity and Specificity of the In Vitro Guinea Pig Papillary Muscle Action Potential Duration for the Assessment of Drug-Induced Torsades De Pointes Liability in Humans

Handbook of experimental pharmacology, 2015, Vol.229, p.205

Ducroq, Joffrey

2015

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Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype–phenotype correlations as a strategy for molecular diagnosis

Human mutation, 2004-04, Vol.23 (4), p.306-317

2004

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The effect of serum matrix and gender on cortisol measurement by commonly used immunoassays

Annals of clinical biochemistry, 2014-05, Vol.51 (3), p.379-385

2014

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Retinal Dehydrogenase 12 ( RDH12) Mutations in Leber Congenital Amaurosis

American journal of human genetics, 2004-10, Vol.75 (4), p.639-646

2004

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Measurement of urinary free cortisol by tandem mass spectrometry and comparison with results obtained by gas chromatography-mass spectrometry and two commercial immunoassays

Annals of clinical biochemistry, 2008-07, Vol.45 (Pt 4), p.380

2008

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Association of spontaneous and procedure-related bleeds with short- and long-term mortality after acute coronary syndromes: an analysis from the PLATO trial

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2015-11, Vol.11 (7), p.737

2015

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Analysis of serum bile acids by isotope dilution-mass spectrometry to assess the performance of routine total bile acid methods

Annals of clinical biochemistry, 2010-11, Vol.47 (Pt 6), p.535

2010

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Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis

American journal of human genetics, 1999-04, Vol.64 (4), p.1225-1228

1999

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Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

European journal of human genetics : EJHG, 2001-08, Vol.9 (8), p.561-571

2001

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Postharvest treatment of mango: Potential use of essential oil with thymol to control anthracnose development

Fruits (1978), 2018-05, Vol.73 (3), p.153-157

2018

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A third locus for dominant optic atrophy on chromosome 22q

Journal of medical genetics, 2005-01, Vol.42 (1), p.e1-e1

2005

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Development of a rapid assay for the analysis of serum cortisol and its implementation into a routine service laboratory

Annals of clinical biochemistry, 2013-07, Vol.50 (Pt 4), p.345

2013

Volltextzugriff (PDF)

Spectrum of retGC1 mutations in Leber's congenital amaurosis

European journal of human genetics : EJHG, 2000-08, Vol.8 (8), p.578-582

2000

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A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3

American journal of human genetics, 1999-04, Vol.64 (4), p.1141-1146

1999

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Human cytomegalovirus-infected cells have unstable assembly of major histocompatibility complex class I complexes and are resistant to lysis by cytotoxic T lymphocytes

Journal of Virology, 1994-05, Vol.68 (5), p.2822-2829

1994

Volltextzugriff (PDF)

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus

Journal of medical genetics, 1999-06, Vol.36 (6), p.447-451

1999

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Leber Congenital Amaurosis

Molecular Genetics and Metabolism, 1999-10, Vol.68 (2), p.200-208

1999

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A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q

European journal of human genetics : EJHG, 2003-12, Vol.11 (12), p.966-971

2003

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Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration

American journal of human genetics, 2000-08, Vol.67 (2), p.487-491

Allikmets, Rando

2000

Volltextzugriff (PDF)

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish inquisition

Human genetics, 2000-09, Vol.107 (3), p.276-284

2000

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Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for IKs

Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for I Ks

Dexrazoxane protects the heart from acute doxorubicin-induced QT prolongation: a key role for IKs : QT Safety

Electrophysiological effects of azimilide in an in vitro model of simulated-ischemia and reperfusion in guinea-pig ventricular myocardium

Pont Vasco de Gama : les fondations maritimes

Sensitivity and Specificity of the In Vitro Guinea Pig Papillary Muscle Action Potential Duration for the Assessment of Drug-Induced Torsades De Pointes Liability in Humans

Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype–phenotype correlations as a strategy for molecular diagnosis

The effect of serum matrix and gender on cortisol measurement by commonly used immunoassays

Retinal Dehydrogenase 12 ( RDH12) Mutations in Leber Congenital Amaurosis

Measurement of urinary free cortisol by tandem mass spectrometry and comparison with results obtained by gas chromatography-mass spectrometry and two commercial immunoassays

Association of spontaneous and procedure-related bleeds with short- and long-term mortality after acute coronary syndromes: an analysis from the PLATO trial

Analysis of serum bile acids by isotope dilution-mass spectrometry to assess the performance of routine total bile acid methods

Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

Postharvest treatment of mango: Potential use of essential oil with thymol to control anthracnose development

A third locus for dominant optic atrophy on chromosome 22q

Development of a rapid assay for the analysis of serum cortisol and its implementation into a routine service laboratory

Spectrum of retGC1 mutations in Leber's congenital amaurosis

A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3

Human cytomegalovirus-infected cells have unstable assembly of major histocompatibility complex class I complexes and are resistant to lysis by cytotoxic T lymphocytes

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus

Leber Congenital Amaurosis

A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q

Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish inquisition

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