Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency: Results from a genotype-phenotype study

Quintavalle, Gabriele
RICCARDI, FEDERICA
Rivolta, Gianna Franca
Martorana, Davide
DI PERNA, Caterina
Percesepe, Antonio
Tagliaferri, Annarita

January 2017

Congenital factor VII (FVII) deficiency is a rare bleeding disorder caused by mutations in F7 gene w...

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.

Bruno Girolami
Elisabetta Cosi
Antonio Girolami
Silvia Ferrari
Anna Maria Lombardi

February 2017

To determine whether heterozygotes with FVII deficiency have a bleeding tendency or not.Eighty-four ...

Advantage Of Registry In Multicenter Study Of Patients With Congenital Rare Bleeding Disorder

Mirbehbahani, N. -B.
Rashidbaghan, A.
Behnampour, N.

February 2015

Introduction: Factor VII deficiency (FVII) is a congenital rare bleeding disorder. It is characteriz...

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Napolitano, M.
Di Minno, M.
Batorova, A.
Dolce, A.
Giansily-Blaizot, M.
Ingerslev, J.
Schved, J.
Auerswald, G.
Kenet, G.
Karimi, M.
Shamsi, T.
Ruiz de S\ue1ez, A.
Dolatkhah, R.
Chuansumrit, A.
Bertrand, M.
Mariani, G.

January 2016

A paucity of data exists on the incidence, diagnosis and treatment of bleeding in women with inherit...

ORIGINAL ARTICLE Factor VII deficiency: defining the clinical picture and optimizing therapeutic options M. LAPECORELLA and G. MARIANI FOR THE INTERNATIONAL REGISTRY ON CONGENITAL FACTOR VII DEFICIENCY

August 2015

Summary. Factor VII (FVII) deficiency is the most frequent among rare congenital bleeding disorders,...

Replacement therapy for bleeding episodes in factor VII deficiency: A prospective evaluation

NAPOLITANO, Mariasanta
Pérez Garrido, R
Batorova, A
Karimi, M
Platokouki,H
Auerswald,G
Bertrand, AM
Di Minno,G
Schved, JF
Bjerre, J
Ingerslev, J
Sørensen, B
Ruiz Saez, A.
MARIANI, Guglielmo
DOLCE, Alberto

January 2013

Patients with inherited factor VII (FVII) deficiency display different clinical phenotypes requiring...

Factor VII deficiency and pregnancy: a case report and review of literature

Zaidi, Syed Mohammad Asad
Qureshi, Rahat
Adil, Salman Naseem

February 2010

Factor VII deficiency is one of the \u27rare inherited disorders of coagulation.\u27 Few cases of Fa...

Major differences in bleeding symptoms between factor VII deficiency and haemophilia B

F. Bernardi
A. Dolce
M. Pinotti
A. D. Shapiro
E. Santagostino
A. Batorova
M. Lapecorella
J. F. Schved
J. Ingerslev
G. Mariani
International Factor VII Deficiency Study Group
F. Peyvandi

May 2009

SUMMARY BACKGROUND: The autosomally-inherited factor VII (FVII) deficiency and X-linked hemophilia B...

Major differences in bleeding symptoms between factor VII deficiency and hemophilia B.

Bernardi F.
Dolce A.
Pinotti M.
Shapiro A.D.
Santagostino E.
Peyvandi F.
Batorova A.
Lapecorella M.
Schved J.F.
Ingerslev J.
Mariani G.

January 2009

SUMMARY BACKGROUND: The autosomally-inherited factor VII (FVII) deficiency and X-linked hemophilia B...

A rare cause of bleeding disorder in pregnancy: Late diagnosed factor VII deficiency: Case report

Şahin, Barbaros
Karabulut, Aysun
Demirtaş, Ömer
Doʇu, M.H.

January 2015

Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

G. Mariani
F. H. Herrmann
A. Dolce
A. Batorova
D. Etro
K. Wulff
J. F. Schved
G. Auerswald
J. Ingerslev
F. Bernardi
International factor VII Deficiency Study Group
F. Peyvandi

March 2005

To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genot...

Recommendation for prophilaxy in congenital factor VII deficiency (comparison between factor VII deficiency and classic hemophilia)

Mirbehbahani, N. B.

March 2012

Background: Inherited factor VII (FVII) deficiency is the most common among rare congenital bleeding...

AND THE STUDY GROUP OF FVII DEFICIENCY* *The Factor VII deficiency study group includes:

Muriel Giansily-blaizot
Régis Verdier
Christine Biron-adréani
Ma Bertr
Chu Besançon
Dr. Jy Borg
Dr. V Lecam
Chu Rouen
Dr. Me
Chu Nancy
Dr. H
Pr. J Goudem
Chu Lille
Dr. R Navarro
Montpellier Dr
A Durin
Correspondence Dr. Muriel

February 2015

Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biologi...

Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency

Di Minno, M.
Dolce, A.
Mariani, G.
STER Study, G.
Auerswald, G.
Batorova, A.
Bernardi, F.
Di Minno, G.
M. N., D.
Dolce, A.
Giansilly Balizot, M.
Ingerslev, J.
Mariani, G.
Martinowitz, U.
Morfini, M.
Napolitano, M.
Pinotti, M.
Shapiro, A.
Schved, J.
S\uf8rensen, B.

January 2013

Individuals with inherited factor VII (FVII) deficiency display bleeding phenotypes ranging from mil...

Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic

Jain S
Donkin J
Frey MJ
Peltier S
Gunawardena S
Cooper DL

November 2018

Shilpa Jain,1,2 Jennifer Donkin,3 Mary-Jane Frey,4 Skye Peltier,5 Sriya Gunawardena,6 David L Cooper...

F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency: Results from a genotype-phenotype study

Quintavalle, Gabriele
RICCARDI, FEDERICA
Rivolta, Gianna Franca
Martorana, Davide
DI PERNA, Caterina
Percesepe, Antonio
Tagliaferri, Annarita

January 2017

Congenital factor VII (FVII) deficiency is a rare bleeding disorder caused by mutations in F7 gene w...

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.

Bruno Girolami
Elisabetta Cosi
Antonio Girolami
Silvia Ferrari
Anna Maria Lombardi

February 2017

To determine whether heterozygotes with FVII deficiency have a bleeding tendency or not.Eighty-four ...

Advantage Of Registry In Multicenter Study Of Patients With Congenital Rare Bleeding Disorder

Mirbehbahani, N. -B.
Rashidbaghan, A.
Behnampour, N.

February 2015

Introduction: Factor VII deficiency (FVII) is a congenital rare bleeding disorder. It is characteriz...

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Napolitano, M.
Di Minno, M.
Batorova, A.
Dolce, A.
Giansily-Blaizot, M.
Ingerslev, J.
Schved, J.
Auerswald, G.
Kenet, G.
Karimi, M.
Shamsi, T.
Ruiz de S\ue1ez, A.
Dolatkhah, R.
Chuansumrit, A.
Bertrand, M.
Mariani, G.

January 2016

A paucity of data exists on the incidence, diagnosis and treatment of bleeding in women with inherit...

ORIGINAL ARTICLE Factor VII deficiency: defining the clinical picture and optimizing therapeutic options M. LAPECORELLA and G. MARIANI FOR THE INTERNATIONAL REGISTRY ON CONGENITAL FACTOR VII DEFICIENCY

August 2015

Summary. Factor VII (FVII) deficiency is the most frequent among rare congenital bleeding disorders,...

Replacement therapy for bleeding episodes in factor VII deficiency: A prospective evaluation

NAPOLITANO, Mariasanta
Pérez Garrido, R
Batorova, A
Karimi, M
Platokouki,H
Auerswald,G
Bertrand, AM
Di Minno,G
Schved, JF
Bjerre, J
Ingerslev, J
Sørensen, B
Ruiz Saez, A.
MARIANI, Guglielmo
DOLCE, Alberto

January 2013

Patients with inherited factor VII (FVII) deficiency display different clinical phenotypes requiring...

Factor VII deficiency and pregnancy: a case report and review of literature

Zaidi, Syed Mohammad Asad
Qureshi, Rahat
Adil, Salman Naseem

February 2010

Factor VII deficiency is one of the \u27rare inherited disorders of coagulation.\u27 Few cases of Fa...

Major differences in bleeding symptoms between factor VII deficiency and haemophilia B

F. Bernardi
A. Dolce
M. Pinotti
A. D. Shapiro
E. Santagostino
A. Batorova
M. Lapecorella
J. F. Schved
J. Ingerslev
G. Mariani
International Factor VII Deficiency Study Group
F. Peyvandi

May 2009

SUMMARY BACKGROUND: The autosomally-inherited factor VII (FVII) deficiency and X-linked hemophilia B...

Major differences in bleeding symptoms between factor VII deficiency and hemophilia B.

Bernardi F.
Dolce A.
Pinotti M.
Shapiro A.D.
Santagostino E.
Peyvandi F.
Batorova A.
Lapecorella M.
Schved J.F.
Ingerslev J.
Mariani G.

January 2009

SUMMARY BACKGROUND: The autosomally-inherited factor VII (FVII) deficiency and X-linked hemophilia B...

A rare cause of bleeding disorder in pregnancy: Late diagnosed factor VII deficiency: Case report

Şahin, Barbaros
Karabulut, Aysun
Demirtaş, Ömer
Doʇu, M.H.

January 2015

Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

G. Mariani
F. H. Herrmann
A. Dolce
A. Batorova
D. Etro
K. Wulff
J. F. Schved
G. Auerswald
J. Ingerslev
F. Bernardi
International factor VII Deficiency Study Group
F. Peyvandi

March 2005

To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genot...

Recommendation for prophilaxy in congenital factor VII deficiency (comparison between factor VII deficiency and classic hemophilia)

Mirbehbahani, N. B.

March 2012

Background: Inherited factor VII (FVII) deficiency is the most common among rare congenital bleeding...

AND THE STUDY GROUP OF FVII DEFICIENCY* *The Factor VII deficiency study group includes:

Muriel Giansily-blaizot
Régis Verdier
Christine Biron-adréani
Ma Bertr
Chu Besançon
Dr. Jy Borg
Dr. V Lecam
Chu Rouen
Dr. Me
Chu Nancy
Dr. H
Pr. J Goudem
Chu Lille
Dr. R Navarro
Montpellier Dr
A Durin
Correspondence Dr. Muriel

February 2015

Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biologi...

Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency

Di Minno, M.
Dolce, A.
Mariani, G.
STER Study, G.
Auerswald, G.
Batorova, A.
Bernardi, F.
Di Minno, G.
M. N., D.
Dolce, A.
Giansilly Balizot, M.
Ingerslev, J.
Mariani, G.
Martinowitz, U.
Morfini, M.
Napolitano, M.
Pinotti, M.
Shapiro, A.
Schved, J.
S\uf8rensen, B.

January 2013

Individuals with inherited factor VII (FVII) deficiency display bleeding phenotypes ranging from mil...

Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic

Jain S
Donkin J
Frey MJ
Peltier S
Gunawardena S
Cooper DL

November 2018

Shilpa Jain,1,2 Jennifer Donkin,3 Mary-Jane Frey,4 Skye Peltier,5 Sriya Gunawardena,6 David L Cooper...

F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency: Results from a genotype-phenotype study

Quintavalle, Gabriele
RICCARDI, FEDERICA
Rivolta, Gianna Franca
Martorana, Davide
DI PERNA, Caterina
Percesepe, Antonio
Tagliaferri, Annarita

January 2017

Congenital factor VII (FVII) deficiency is a rare bleeding disorder caused by mutations in F7 gene w...

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.

Bruno Girolami
Elisabetta Cosi
Antonio Girolami
Silvia Ferrari
Anna Maria Lombardi

February 2017

To determine whether heterozygotes with FVII deficiency have a bleeding tendency or not.Eighty-four ...

Advantage Of Registry In Multicenter Study Of Patients With Congenital Rare Bleeding Disorder

Mirbehbahani, N. -B.
Rashidbaghan, A.
Behnampour, N.

February 2015

Introduction: Factor VII deficiency (FVII) is a congenital rare bleeding disorder. It is characteriz...

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Abstract

Extracted data

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Abstract

Extracted data

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