M. Neerman-Arbez: search on Z-Library

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1

Molecular Basis of Fibrinogen Deficiency

Neerman-Arbez, M.

Journal:

Pathophysiology of Haemostasis and Thrombosis

Year:

2006

Language:

english

File:

PDF, 744 KB

english, 2006

2

Congenital Fibrinogen Disorders: An Update

de Moerloose, Philippe, Casini, Alessandro, Neerman-Arbez, Marguerite

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2013

Language:

english

File:

PDF, 287 KB

english, 2013

3

Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders

Neerman-Arbez, Marguerite, de Moerloose, Philippe, Casini, Alessandro

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2016

Language:

english

File:

PDF, 608 KB

english, 2016

4

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management

Casini, A., Neerman-Arbez, M., Ariëns, R. A., de Moerloose, P.

Journal:

Journal of Thrombosis and Haemostasis

Year:

2015

Language:

english

File:

PDF, 292 KB

english, 2015

5

Mutational Epidemiology of Congenital Fibrinogen Disorders

Casini, Alessandro, Blondon, Marc, Tintillier, Veronique, Goodyer, Matthew, Sezgin, Melike, Gunes, Adalet, Hanss, Michel, de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Thrombosis and Haemostasis

Year:

2018

Language:

english

File:

PDF, 201 KB

english, 2018

6

Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations

Marguerite Neerman-Arbez, Philippe de Moerloose

Journal:

Year:

2007

Language:

english

File:

PDF, 284 KB

english, 2007

7

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in theFGAandFGGgenes

M. Neerman-Arbez, P. de Moerloose, A. Honsberger, G. Parlier, B. Arnuti, C. Biron, J.-Y. Borg, S. Eber, E. Meili, K. Peter-Salonen, L. Ripoll, C. Vervel, R. d' Oiron, P. Staeger, S. Antonarakis, M. Mo

Journal:

Year:

2001

Language:

english

File:

PDF, 56 KB

english, 2001

8

Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins

D. VU, M. NEERMAN-ARBEZ

Journal:

Journal of Thrombosis and Haemostasis

Year:

2007

Language:

english

File:

PDF, 269 KB

english, 2007

9

To aggregate or not to aggregate…

M. NEERMAN-ARBEZ

Journal:

Journal of Thrombosis and Haemostasis

Year:

2007

Language:

english

File:

PDF, 442 KB

english, 2007

10

Fibrinogen Gene Mutations Accounting for Congenital Afibrinogenemia

MARGUERITE NEERMAN-ARBEZ

Journal:

Annals of the New York Academy of Sciences

Year:

2001

Language:

english

File:

PDF, 675 KB

english, 2001

11

The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster

Neerman-Arbez, Marguerite, Antonarakis, Stylianos E, Honsberger, Ariane, Morris, Michael A

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 340 KB

english, 1999

12

Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia

Isabelle Tchou, Myriam Diepold, Pierre-Antonio Pilotto, Dorine Swinkels, Marguerite Neerman-Arbez, Photis Beris

Journal:

European Journal of Haematology

Year:

2009

Language:

english

File:

PDF, 482 KB

english, 2009

13

Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family

Tchou Isabelle, Neerman-Arbez Marguerite, Beris Photis

Journal:

European Journal of Haematology

Year:

2011

Language:

english

File:

PDF, 186 KB

english, 2011

14

Coexisting dysfibrinogenemia (γArg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete)

A. Travlou, A. Gialeraki, E. Merkouri, M. Politou, A. Sfyridaki, M. Neerman-Arbez

Journal:

Thrombosis Research

Year:

2010

Language:

english

File:

PDF, 137 KB

english, 2010

15

Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12

Marc Friedli, Michel Guipponi, Sonia Bertrand, Daniel Bertrand, Marguerite Neerman-Arbez, Hamish S. Scott, Stylianos E. Antonarakis, Alexandre Reymond

Journal:

Year:

2003

Language:

english

File:

PDF, 1.05 MB

english, 2003

16

An isolated exclusion in the FGA system

U.-D. Immel, M. Kleiber, M. Neerman-Arbez, M. Klintschar

Journal:

International Congress Series

Year:

2004

Language:

english

File:

PDF, 152 KB

english, 2004

17

The Locus for Combined Factor V-Factor VIII Deficiency (F5F8D) Maps to 18q21, between D18S849 and D18S1103

M. Neerman-Arbez, S.E. Antonarakis, J.-L. Blouin, S. Zeinali, M. Akhtari, Y. Afshar, E.G.D. Tuddenham

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 152 KB

english, 1997

18

Fibrinogen Gdansk: Hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro)

Mital, Andrzej, Undas, Anetta, Neerman-Arbez, Marguerite, Hellmann, Andrzej

Journal:

Thrombosis Research

Year:

2012

Language:

english

File:

PDF, 143 KB

english, 2012

19

High incidence of ectopic nucleolar organizer regions in human testicular tumors

Marguerite Neerman-Arbez, Celia D. DeLozier-Blanchet, Jean-François Bolle, Raymond Rondez, Michael Morris

Journal:

Cancer Genetics and Cytogenetics

Year:

1993

Language:

english

File:

PDF, 521 KB

english, 1993

20

Fibrinogen Krakow: A novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function

Undas, Anetta, Zdziarska, Joanna, Iwaniec, Teresa, Stepien, Ewa, Skotnicki, Aleksander B., de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Thrombosis and Haemostasis

Year:

2009

Language:

english

File:

PDF, 96 KB

english, 2009

21

Functional characterisation of plasma fibrin clots in Polish carriers of fibrinogen γArg275His mutation (fibrinogen Zabrze)

Undas, A., Pastuszczak, M., Iwaniec, T., Kapelak, K., Neerman-Arbez, M.

Journal:

Thrombosis and Haemostasis

Year:

2010

Language:

english

File:

PDF, 145 KB

english, 2010

22

Fibrinogen gene regulation

Fish, R. J., Neerman-Arbez, M.

Journal:

Thrombosis and Haemostasis

Year:

2012

Language:

english

File:

PDF, 166 KB

english, 2012

23

FGB mutations leading to congenital quantitative fibrinogen deficiencies: An update and report of four novel mutations

Casini, A., Lukowski, S., Quintard, V. Louvain, Crutu, A., Zak, M., Regazzoni, S., de Moerloose, P., Neerman-Arbez, M.

Journal:

Thrombosis Research

Year:

2014

Language:

english

File:

PDF, 921 KB

english, 2014

24

Thromboelastographic phenotypes of fibrinogen and its variants: Clinical and non-clinical implications

Galanakis, Dennis K., Neerman-Arbez, Marguerite, Brennan, Stephen, Rafailovich, Miriam, Hyder, Luke, Travlou, Oreanthi, Papadakis, Emmanuel, Manco-Johnson, Marilyn J., Henschen, Agnes, Scharrer, Inge

Journal:

Thrombosis Research

Year:

2014

Language:

english

File:

PDF, 1.24 MB

english, 2014

25

Treatment of congenital fibrinogen disorders

de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Expert Opinion on Biological Therapy

Year:

2008

Language:

english

File:

PDF, 494 KB

english, 2008

26

Des-(27-31)C-Peptide: A NOVEL SECRETORY PRODUCT OF THE RAT PANCREATIC BETA CELL PRODUCED BY TRUNCATION OF PROINSULIN CONNECTING PEPTIDE IN SECRETORY GRANULES

Verchere, C. B., Paoletta, M., Neerman-Arbez, M., Rose, K., Irminger, J.-C., Gingerich, R. L., Kahn, S. E., Halban, P. A.

Journal:

Journal of Biological Chemistry

Year:

1996

Language:

english

File:

PDF, 748 KB

english, 1996

27

In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes

Stroka, D., Keogh, A., Vu, D., Fort, A., Stoffel, M. H., Kühni-Boghenbor, K., Furer, C., Banz, V., Demarmels Biasiutti, F., Lämmle, B., Candinas, D., Neerman-Arbez, M.

Journal:

Journal of Thrombosis and Haemostasis

Year:

2014

Language:

english

File:

PDF, 666 KB

english, 2014

28

Fibrinogen geneva II

Casini, Alessandro, De Maistre, Emmanuel, Casini-Stuppi, Virginie, Fontana, Pierre, Neerman-Arbez, Marguerite, de Moerloose, Philippe

Journal:

Blood Coagulation & Fibrinolysis

Year:

2014

Language:

english

File:

PDF, 97 KB

english, 2014

29

Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes

Lukowski, Samuel W., Fish, Richard J., Martin-Levilain, Juliette, Gonelle-Gispert, Carmen, Bühler, Leo H., Maechler, Pierre, Dermitzakis, Emmanouil T., Neerman-Arbez, Marguerite

Journal:

Year:

2015

Language:

english

File:

PDF, 2.20 MB

english, 2015

30

Loss of Dicer in Sertoli Cells Has a Major Impact on the Testicular Proteome of Mice

Papaioannou, M. D., Lagarrigue, M., Vejnar, C. E., Rolland, A. D., Kuhne, F., Aubry, F., Schaad, O., Fort, A., Descombes, P., Neerman-Arbez, M., Guillou, F., Zdobnov, E. M., Pineau, C., Nef, S.

Journal:

Molecular & Cellular Proteomics

Year:

2011

Language:

english

File:

PDF, 1.97 MB

english, 2011

31

Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis

Lebreton, A., Casini, A., Alhayek, R., Kouteich, K. L., Neerman-Arbez, M., de Moerloose, P.

Journal:

Year:

2015

Language:

english

File:

PDF, 224 KB

english, 2015

32

Fibrinogen and the Risk of Thrombosis

de Moerloose, Philippe, Boehlen, Françoise, Neerman-Arbez, Marguerite

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2010

Language:

english

File:

PDF, 176 KB

english, 2010

33

Congenital Fibrinogen Disorders

de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2009

Language:

english

File:

PDF, 233 KB

english, 2009

34

Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants

Vu, D., Di Sanza, C., Neerman-Arbez, M.

Journal:

Year:

2008

Language:

english

File:

PDF, 313 KB

english, 2008

35

The GM2-1 Ganglioside Islet Autoantigen in Insulin-Dependent Diabetes Mellitus Is Expressed in Secretory Granules and Is Notβ -Cell Specific 1

Dotta, Francesco, Previti, Marcello, Neerman-Arbez, Marguerite, Dionisi, Sabrina, Cucinotta, Domenico, Lenti, Luisa, Di Mario, Umberto, Halban, Philippe A.

Journal:

Year:

1998

Language:

english

File:

PDF, 314 KB

english, 1998

36

Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes

Lukowski, Samuel W., Fish, Richard J., Martin-Levilain, Juliette, Gonelle-Gispert, Carmen, Bühler, Leo H., Maechler, Pierre, Dermitzakis, Emmanouil T., Neerman-Arbez, Marguerite

Journal:

Year:

2015

Language:

english

File:

PDF, 170 KB

english, 2015

37

Clinical Features and Management of Congenital Fibrinogen Deficiencies

Casini, Alessandro, de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Seminars in Thrombosis and Hemostasis

Year:

2016

Language:

english

File:

PDF, 187 KB

english, 2016

38

Severe factor XI deficiency in a Lebanese family

de Moerloose, Philippe, Germanos-Haddad, Myrna, Boehlen, Fran??oise, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2004

Language:

english

File:

PDF, 95 KB

english, 2004

39

Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the γAla82Gly mutation

Zdziarska, Joanna, Undas, Anetta, Basa, Joanna, Iwaniec, Teresa, Skotnicki, Aleksander B, de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2009

Language:

english

File:

PDF, 123 KB

english, 2009

40

Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature

Casini, A., Sokollik, C., Lukowski, S. W., Lurz, E., Rieubland, C., de Moerloose, P., Neerman-Arbez, M.

Journal:

Year:

2015

Language:

english

File:

PDF, 474 KB

english, 2015

41

Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding

Priovolos, Anna, Neerman-Arbez, Marguerite, Morris, Michael, Angelillo-Scherrer, Anne, Nötzli, Jasmine

Journal:

Blood Coagulation & Fibrinolysis

Year:

2015

Language:

english

File:

PDF, 148 KB

english, 2015

42

Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency

Tirefort, Yordanka, Uhr, Mario R., Neerman-Arbez, Marguerite, de Moerloose, Philippe

Journal:

Blood Coagulation & Fibrinolysis

Year:

2012

Language:

english

File:

PDF, 71 KB

english, 2012

43

Fibrinogen Gamma375 Arg???Trp Mutation (Fibrinogen Aguadilla) Causes Hereditary Hypofibrinogenemia, Hepatic Endoplasmic Reticulum Storage Disease and Cirrhosis

Rubbia-Brandt, Laura, Neerman-Arbez, Marguerite, Rougemont, Anne-Laure, Mal??, Pierre-Jean, Spahr, Laurent

Journal:

American Journal of Surgical Pathology

Year:

2006

Language:

english

File:

PDF, 544 KB

english, 2006

44

A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis

Robert-Ebadi, Helia, Le Querrec, Agnès, de Moerloose, Philippe, Gandon-Laloum, Sylvie, Borel Derlon, Annie, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2008

Language:

english

File:

PDF, 62 KB

english, 2008

45

Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients

Abdel Wahab, Magy, de Moerloose, Philippe, Fish, Richard J, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2010

Language:

english

File:

PDF, 314 KB

english, 2010

46

A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream

Robert-Ebadi, H, de Moerloose, P, Khorassani, M El, Khattab, M El, Neerman-Arbez, M

Journal:

Blood Coagulation & Fibrinolysis

Year:

2009

Language:

english

File:

PDF, 119 KB

english, 2009

47

Decreased plasmin resistance by clots of a homophenotypic Aα R 16H fibrinogen (Kingsport, slower fibrinopeptide A than fibrinopeptide B release)

Galanakis, Dennis K, Neerman-Arbez, Marguerite, Kudryk, Bohdan, Henschen, Agnes

Journal:

Blood Coagulation & Fibrinolysis

Year:

2010

Language:

english

File:

PDF, 385 KB

english, 2010

48

Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia

Tirefort, Yordanka, Alson, Olivat Rakoto, de Moerloose, Philippe, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2012

Language:

english

File:

PDF, 115 KB

english, 2012

49

Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects

Miesbach, Wolfgang, Scharrer, Inge, Henschen, Agnes, Neerman-Arbez, Marguerite, Spitzer, Silvia, Galanakis, Dennis

Journal:

Blood Coagulation & Fibrinolysis

Year:

2010

Language:

english

File:

PDF, 296 KB

english, 2010

50

A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family

Levrat, Emmanuel, Aboukhamis, Imad, de Moerloose, Philippe, Farho, Jaafar, Chamaa, Sahar, Reber, Guido, Fort, Alexandre, Neerman-Arbez, Marguerite

Journal:

Blood Coagulation & Fibrinolysis

Year:

2011

Language:

english

File:

PDF, 150 KB

english, 2011