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M.S. Médecine sciences, 2004-06, Vol.20 (6-7), p.615-615

Garbarz, Michel

2004

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Pharmacy workload benchmarking: Establishing a health-system outpatient infusion productivity metric

Journal of oncology pharmacy practice, 2019-01, Vol.25 (1), p.172-178

2019

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Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin αI variants

British journal of haematology, 1993-11, Vol.85 (3), p.584-595

1993

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Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis

Human mutation, 1995, Vol.5 (4), p.339-340

1995

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Comparison of Hospital Mortality During ST-Segment Elevation Myocardial Infarction in the Era of Reperfusion Therapy in Women Versus Men and in Older Versus Younger Patients

The American journal of cardiology, 2013-06, Vol.111 (12), p.1708-1713

2013

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Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPI

Arteriosclerosis, thrombosis, and vascular biology, 1999-04, Vol.19 (4), p.862-869

1999

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Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis

American journal of human genetics, 1992-08, Vol.51 (2), p.440-442

1992

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Spectrin αIIa variant in dominant and non-dominant spherocytosis

Human genetics, 1993-09, Vol.92 (2), p.153-156

1993

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Erythroid expression of the human alpha-spectrin gene promoter is mediated by GATA-1- and NF-E2-binding proteins

The Journal of biological chemistry, 2002-11, Vol.277 (44), p.41563-41570

2002

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A variant of spectrin low‐expression allele αLELY carrying a hereditary elliptocytosis mutation in codon 28

British journal of haematology, 1994-11, Vol.88 (3), p.534-540

1994

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Elliptocytosis‐associated spectrin Rouen (β220/218) has a truncated but still phosphorylatable β chain

British journal of haematology, 1992-02, Vol.80 (2), p.242-250

1992

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Characterization of rat hepatocyte plasma membrane domains by monoclonal antibodies

European journal of cell biology, 1985-11, Vol.39 (1), p.122-129

1985

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Severe recessive poikilocytic anaemia with a new spectrin α chain variant

British journal of haematology, 1990-04, Vol.74 (4), p.497-507

1990

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Spectrin beta-chain variant associated with hereditary elliptocytosis

The Journal of clinical investigation, 1982-10, Vol.70 (4), p.707-715

1982

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Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Blood, 1989-08, Vol.74 (2), p.828-832

1989

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Abnormal tryptic peptide from the spectrin α‐chain resulting from α‐ or β‐chain mutations: two genetically distinct forms of the Sp αI/74 variant

British journal of haematology, 1990-11, Vol.76 (3), p.406-413

1990

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Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects

British journal of haematology, 1997-07, Vol.98 (1), p.32-40

1997

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Erythroid Expression of the Human [alpha]-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins

The Journal of biological chemistry, 2002-11, Vol.277 (44), p.41563-41570

2002

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Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

British journal of haematology, 1996-10, Vol.95 (1), p.57-66

1996

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The Characterization of Protein 4.1 Presles, a Shortened Variant of RBC Membrane Protein 4.1

Blood, 1985-06, Vol.65 (6), p.1511-1517

1985

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Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-association

The Journal of clinical investigation, 1990-09, Vol.86 (3), p.909-916

1990

Volltextzugriff (PDF)

Détection du messager chimérique abl-bcr dans la leucémie myéloïde chronique

M.S. Médecine sciences, 1988, Vol.4 (7), p.402

1988

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Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

Blood, 1986-06, Vol.67 (6), p.1661-1667

1986

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A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis

The Journal of clinical investigation, 1996-01, Vol.97 (2), p.373-380

1996

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Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis

Clinical and experimental immunology, 1981-01, Vol.43 (1), p.87-93

1981

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Heatwave

Pharmacy workload benchmarking: Establishing a health-system outpatient infusion productivity metric

Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin αI variants

Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis

Comparison of Hospital Mortality During ST-Segment Elevation Myocardial Infarction in the Era of Reperfusion Therapy in Women Versus Men and in Older Versus Younger Patients

Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPI

Fast screening methods to detect mutations of spectrin in subjects with hereditary elliptocytosis

Spectrin αIIa variant in dominant and non-dominant spherocytosis

Erythroid expression of the human alpha-spectrin gene promoter is mediated by GATA-1- and NF-E2-binding proteins

A variant of spectrin low‐expression allele αLELY carrying a hereditary elliptocytosis mutation in codon 28

Elliptocytosis‐associated spectrin Rouen (β220/218) has a truncated but still phosphorylatable β chain

Characterization of rat hepatocyte plasma membrane domains by monoclonal antibodies

Severe recessive poikilocytic anaemia with a new spectrin α chain variant

Spectrin beta-chain variant associated with hereditary elliptocytosis

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Abnormal tryptic peptide from the spectrin α‐chain resulting from α‐ or β‐chain mutations: two genetically distinct forms of the Sp αI/74 variant

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects

Erythroid Expression of the Human [alpha]-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

The Characterization of Protein 4.1 Presles, a Shortened Variant of RBC Membrane Protein 4.1

Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-association

Détection du messager chimérique abl-bcr dans la leucémie myéloïde chronique

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis

Anti-spectrin in sera containing smooth muscle autoantibodies from patients with chronic active hepatitis

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