UB Paderborn / Katalog / Suche / in CDI

Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium

Clinical genetics, 2021-05, Vol.99 (5), p.662-672

2021

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Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis

American journal of hematology, 2016-12, Vol.91 (12), p.1202-1205

2016

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Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations

British journal of haematology, 2013-07, Vol.162 (2), p.278-281

2013

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Non-HFE hemochromatosis: Pathophysiological and diagnostic aspects

Clinics and research in hepatology and gastroenterology, 2014-04, Vol.38 (2), p.143-154

2014

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Long-term response to rituximab and fludarabine combination in IgM anti-myelin-associated glycoprotein neuropathy

Journal of the peripheral nervous system, 2011-09, Vol.16 (3), p.180-185

2011

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Spontaneous and stimulated secretion of monocyte chemotactic protein-1 and macrophage migration inhibitory factor by peritoneal macrophages in women with and without endometriosis

Fertility and sterility, 2002-05, Vol.77 (5), p.989-994

2002

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Magasin des enfans ou dialogues entre une sage gouvernante et plusieurs de ses élèves

[Jeanne-Marie] Le Prince de Beaumont / Frédéric Hermann / Frédéric Hermann

2022

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Jeanne-Marie Le Prince de Beaumont: Magazin des enfans, ou dialogues entre une sage gouvernante et plusieurs de ses 'l'ves

2021

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Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload

Blood cells, molecules, & diseases, 2015-02, Vol.54 (2), p.151-154

2015

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Perinatal morbidity among women with a previous caesarean delivery (PRISMA trial): a cluster-randomised trial

The Lancet (British edition), 2024-01, Vol.403 (10421), p.44-54

2024

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Genetics of neural tube defects: new candidate genes and complex mode of inheritance

European journal of human genetics : EJHG, 2022-04, Vol.30 (SUPPL 1), p.351-352

2022

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Clinical characteristics and outcome of 318 families with familial monoclonal gammopathy: A multicenter Intergroupe Francophone du Myélome study

American journal of hematology, 2023-02, Vol.98 (2), p.264-271

2023

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Accurate classification of plasma cell dyscrasias is achieved by combining artificial intelligence and flow cytometry

British journal of haematology, 2022-03, Vol.196 (5), p.1175-1183

2022

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Clinical characteristics and outcome of 318 families with familial monoclonal gammopathy: A multicenter Intergroupe Francophone du Myélome study

American journal of hematology, 2023-01, Vol.98 (2), p.264-271

2023

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The lenalidomide/bortezomib/dexamethasone regimen for the treatment of blastic plasmacytoid dendritic cell neoplasm

Hematological oncology, 2019-10, Vol.37 (4), p.487-489

2019

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Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders

Human genetics, 2019-04, Vol.138 (4), p.363-374

2019

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Sequential Allogeneic Transplantation for Multiple Myeloma Patient in Early Relapse Post-Autograft

Blood, 2016-12, Vol.128 (22), p.5768-5768

2016

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Jeanne-Marie Le Prince de Beaumont: Magazin des enfans, ou dialogues entre une sage gouvernante et plusieurs de ses 'l'ves

2021

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Evolving characteristics and outcome of secondary acute promyelocytic leukemia (APL): A prospective analysis by the French‐Belgian‐Swiss APL group

Cancer, 2015-07, Vol.121 (14), p.2393-2399

2015

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Evolving characteristics and outcome of secondary acute promyelocytic leukemia ( APL ): A prospective analysis by the F rench‐ B elgian‐ S wiss APL group

Cancer, 2015-07, Vol.121 (14), p.2393-2399

2015

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Beauty and the beast and other classic stories

Beaumont, Jeanne Marie Leprince de

2017

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Beauty and the Beast and Other Classic Stories

Leprince de Beaumont, Jeanne-Marie

2017

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Fifteen Views of a Christening Gown

Ploughshares, 2014-12, Vol.40 (4), p.8-9

BEAUMONT, JEANNE MARIE

2014

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Portrait with Closed Eyes

Ploughshares, 2014-12, Vol.40 (4), p.10-10

BEAUMONT, JEANNE MARIE

2014

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Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium

Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis

Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations

Non-HFE hemochromatosis: Pathophysiological and diagnostic aspects

Long-term response to rituximab and fludarabine combination in IgM anti-myelin-associated glycoprotein neuropathy

Spontaneous and stimulated secretion of monocyte chemotactic protein-1 and macrophage migration inhibitory factor by peritoneal macrophages in women with and without endometriosis

Magasin des enfans ou dialogues entre une sage gouvernante et plusieurs de ses élèves

Jeanne-Marie Le Prince de Beaumont: Magazin des enfans, ou dialogues entre une sage gouvernante et plusieurs de ses 'l'ves

Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload

Perinatal morbidity among women with a previous caesarean delivery (PRISMA trial): a cluster-randomised trial

Genetics of neural tube defects: new candidate genes and complex mode of inheritance

AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer

Clinical characteristics and outcome of 318 families with familial monoclonal gammopathy: A multicenter Intergroupe Francophone du Myélome study

Accurate classification of plasma cell dyscrasias is achieved by combining artificial intelligence and flow cytometry

Clinical characteristics and outcome of 318 families with familial monoclonal gammopathy: A multicenter Intergroupe Francophone du Myélome study

The lenalidomide/bortezomib/dexamethasone regimen for the treatment of blastic plasmacytoid dendritic cell neoplasm

Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders

Sequential Allogeneic Transplantation for Multiple Myeloma Patient in Early Relapse Post-Autograft

Jeanne-Marie Le Prince de Beaumont: Magazin des enfans, ou dialogues entre une sage gouvernante et plusieurs de ses 'l'ves

Evolving characteristics and outcome of secondary acute promyelocytic leukemia (APL): A prospective analysis by the French‐Belgian‐Swiss APL group

Evolving characteristics and outcome of secondary acute promyelocytic leukemia ( APL ): A prospective analysis by the F rench‐ B elgian‐ S wiss APL group

Beauty and the beast and other classic stories

Beauty and the Beast and Other Classic Stories

Fifteen Views of a Christening Gown

Portrait with Closed Eyes

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