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Low-Flow, Low-Gradient Severe Aortic Stenosis Despite Normal Ejection Fraction Is Associated With Severe Left Ventricular Dysfunction as Assessed by Speckle-Tracking Echocardiography: A Multicenter Study

Circulation. Cardiovascular imaging, 2012, Vol.5 (1), p.27-35

2012

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Le viaduc de Belle-Feuille à Joinville (RN 67) en Haute-Marne

Travaux (Paris), 1993 (692), p.27-36

1993

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Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Blood, 2001-01, Vol.97 (2), p.399-403

2001

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International longitudinal registry of patients with atrial fibrillation and treated with rivaroxaban: RIVaroxaban Evaluation in Real life setting (RIVER)

Thrombosis journal, 2019-04, Vol.17 (1), p.7-7, Article 7

2019

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Occurrence of myeloproliferative disorder in patients with Noonan syndrome

The Journal of pediatrics, 1997-06, Vol.130 (6), p.885-889

1997

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Low-flow low-gradient aortic stenosis: Prognostic impact and effect of surgery

Archives of cardiovascular diseases, 2011-04, Vol.104 (4), p.294-294

2011

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Dyserythropoiesis associated with a Fas‐deficient condition in childhood

British journal of haematology, 2000-02, Vol.108 (2), p.300-304

2000

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Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha‐interferon therapy

British journal of haematology, 2000-08, Vol.110 (2), p.420-423

2000

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Refractory anaemia and mitochondrial cytopathy in childhood

British journal of haematology, 1994-06, Vol.87 (2), p.381-385

1994

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Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis

Blood, 1993-04, Vol.81 (8), p.2014-2020

1993

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Suppression of CDA II expression in a homozygote

British journal of haematology, 1999-09, Vol.106 (4), p.948-953

1999

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Myelodysplastic Syndromes In Childhood: Is the FAB Classification Relevant? Report of 81 Children From a French Multicentre Study

Leukemia & lymphoma, 1998, Vol.28 (5-6), p.531-540

1998

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The GEN.S : a fortuitous finding of a routine screening test for hereditary spherocytosis

Hematology and cell therapy, 1999-06, Vol.41 (3), p.113-116

1999

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Myelodysplastic syndromes in childhood: report of 49 patients from a French multicentre study

British journal of haematology, 1996-01, Vol.92 (2), p.344-350

1996

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Parvovirus infection, leukaemia, and immunodeficiency

The Lancet (British edition), 1989-01, Vol.1 (8629), p.101

1989

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Hematologic involvement in mitochondrial cytopathies in childhood : A retrospective study of bone marrow smears

Pediatric research, 1999-08, Vol.46 (2), p.158-162

1999

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Une anémie sidéroblastique chez un malade en alimentation entérale exclusive prolongée

Nutrition clinique et métabolisme, 1998-10, Vol.12 (3), p.222-223

1998

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PARVOVIRUS INFECTION, LEUKAEMIA, AND IMMUNODEFICIENCY

The Lancet (British edition), 1989-01, Vol.333 (8629), p.101-102

1989

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Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the groupe français de cytogénétique hématologique

Leukemia, 1997-09, Vol.11 (9), p.1478-1485

Groupe Franc¸ais de Cytoge´ne´tique He´matologique

1997

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Trilineage response to recombinant human granulocyte colony‐stimulating factor administration in a patient with myelodysplastic syndrome

American journal of hematology, 1993-05, Vol.43 (1), p.76-77

1993

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Myélodysplasies de l'enfant et cytopathies mitochondriales: Les syndromes myélodysplasiques (1ère partie)

Pathologie biologie (Paris), 1997, Vol.45 (7), p.594-599

1997

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Myeoldysplastic syndromes in chilhood : report of 49 patients from a French multicentre study

British journal of haematology, 1996, Vol.92 (2), p.344-350

1996

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Elliptocytose chez un sujet de race noire : un piège diagnostique ou « ne vous fiez pas aux apparences

Hématologie, 2001, Vol.7 (4), p.297-299

2001

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Low-Flow, Low-Gradient Severe Aortic Stenosis Despite Normal Ejection Fraction Is Associated With Severe Left Ventricular Dysfunction as Assessed by Speckle-Tracking Echocardiography: A Multicenter Study

Le viaduc de Belle-Feuille à Joinville (RN 67) en Haute-Marne

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

International longitudinal registry of patients with atrial fibrillation and treated with rivaroxaban: RIVaroxaban Evaluation in Real life setting (RIVER)

Response to Letter Regarding Article, “Low-Flow, Low-Gradient Severe Aortic Stenosis Despite Normal Ejection Fraction Is Associated With Severe Left Ventricular Dysfunction as Assessed by Speckle-Tracking Echocardiography: A Multicenter Study”

Occurrence of myeloproliferative disorder in patients with Noonan syndrome

Low-flow low-gradient aortic stenosis: Prognostic impact and effect of surgery

Dyserythropoiesis associated with a Fas‐deficient condition in childhood

Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha‐interferon therapy

Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl–Lewis-X antigen in leukocytes—a new syndrome?

Refractory anaemia and mitochondrial cytopathy in childhood

Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis

Suppression of CDA II expression in a homozygote

Myelodysplastic Syndromes In Childhood: Is the FAB Classification Relevant? Report of 81 Children From a French Multicentre Study

The GEN.S : a fortuitous finding of a routine screening test for hereditary spherocytosis

Myelodysplastic syndromes in childhood: report of 49 patients from a French multicentre study

Parvovirus infection, leukaemia, and immunodeficiency

Hematologic involvement in mitochondrial cytopathies in childhood : A retrospective study of bone marrow smears

Une anémie sidéroblastique chez un malade en alimentation entérale exclusive prolongée

PARVOVIRUS INFECTION, LEUKAEMIA, AND IMMUNODEFICIENCY

Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the groupe français de cytogénétique hématologique

Trilineage response to recombinant human granulocyte colony‐stimulating factor administration in a patient with myelodysplastic syndrome

Myélodysplasies de l'enfant et cytopathies mitochondriales: Les syndromes myélodysplasiques (1ère partie)

Myeoldysplastic syndromes in chilhood : report of 49 patients from a French multicentre study

Elliptocytose chez un sujet de race noire : un piège diagnostique ou « ne vous fiez pas aux apparences

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