-
2
-
-
0034661804
-
Hereditary angioedema with normal C1-inhibitor activity in women
-
K. Bork, S.E. Barnstedt, P. Koch, H. Traupe Hereditary angioedema with normal C1-inhibitor activity in women Lancet 356 2000 213 217
-
(2000)
Lancet
, vol.356
, pp. 213-217
-
-
Bork, K.1
Barnstedt, S.E.2
Koch, P.3
Traupe, H.4
-
3
-
-
0034508657
-
Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema
-
K.E. Binkley, A. Davis Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema J Allergy Clin Immunol 106 2000 546 550
-
(2000)
J Allergy Clin Immunol
, vol.106
, pp. 546-550
-
-
Binkley, K.E.1
Davis, A.2
-
4
-
-
33646026697
-
Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor
-
G. Dewald, K. Bork Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor Biochem Biophys Res Commun 343 2006 1286 1289
-
(2006)
Biochem Biophys Res Commun
, vol.343
, pp. 1286-1289
-
-
Dewald, G.1
Bork, K.2
-
5
-
-
33845219794
-
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III
-
S. Cichon, L. Martin, H.C. Hennies Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III Am J Hum Genet 79 2006 1098 1104
-
(2006)
Am J Hum Genet
, vol.79
, pp. 1098-1104
-
-
Cichon, S.1
Martin, L.2
Hennies, H.C.3
-
6
-
-
77956438524
-
Type III hereditary angio-oedema: Clinical and biological features in a French cohort
-
V. Vitrat-Hincky, A. Gompel, C. Dumestre-Perard Type III hereditary angio-oedema: clinical and biological features in a French cohort Allergy 65 2010 1331 1336
-
(2010)
Allergy
, vol.65
, pp. 1331-1336
-
-
Vitrat-Hincky, V.1
Gompel, A.2
Dumestre-Perard, C.3
-
7
-
-
67649227073
-
Hereditary angioedema caused by missense mutations in the factor XII gene: Clinical features, trigger factors and therapy
-
K. Bork, K. Wulff, J. Hardt, G. Witzke, P. Staubach Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors and therapy J Allergy Clin Immunol 124 2009 129 134
-
(2009)
J Allergy Clin Immunol
, vol.124
, pp. 129-134
-
-
Bork, K.1
Wulff, K.2
Hardt, J.3
Witzke, G.4
Staubach, P.5
-
8
-
-
80053130267
-
A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor
-
K. Bork, K. Wulff, P. Meinke, N. Wagner, J. Hardt, G. Witzke A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor Clin Immunol 141 2011 31 35
-
(2011)
Clin Immunol
, vol.141
, pp. 31-35
-
-
Bork, K.1
Wulff, K.2
Meinke, P.3
Wagner, N.4
Hardt, J.5
Witzke, G.6
-
10
-
-
63649128831
-
Genetic analysis of factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema
-
Q.L. Duan, K. Binkley, G.A. Rouleau Genetic analysis of factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema J Allergy Clin Immunol 123 2009 906 910
-
(2009)
J Allergy Clin Immunol
, vol.123
, pp. 906-910
-
-
Duan, Q.L.1
Binkley, K.2
Rouleau, G.A.3
-
11
-
-
80053361954
-
Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions
-
K. Binkley Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions Allergy Asthma Clin Immunol 6 2010 16
-
(2010)
Allergy Asthma Clin Immunol
, vol.6
, pp. 16
-
-
Binkley, K.1
-
12
-
-
68349117147
-
Hereditary angioedema with normal C1 inhibition
-
K. Bork Hereditary angioedema with normal C1 inhibition Curr Allergy Asthma Rep 9 2009 280 285
-
(2009)
Curr Allergy Asthma Rep
, vol.9
, pp. 280-285
-
-
Bork, K.1
-
13
-
-
0037356703
-
Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy
-
K. Bork, B. Fischer, G. Dewald Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy Am J Med 114 2003 294 298
-
(2003)
Am J Med
, vol.114
, pp. 294-298
-
-
Bork, K.1
Fischer, B.2
Dewald, G.3
-
14
-
-
33750527356
-
Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations
-
K. Bork Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations Immunol Allergy Clin N Am 26 2006 709 724
-
(2006)
Immunol Allergy Clin N Am
, vol.26
, pp. 709-724
-
-
Bork, K.1
-
15
-
-
34948849184
-
Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene
-
L. Martin, N. Raison-Peyron, M. Nthen, S. Cichon, C. Drouet Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene J Allergy Clin Immunol 120 2007 975 977
-
(2007)
J Allergy Clin Immunol
, vol.120
, pp. 975-977
-
-
Martin, L.1
Raison-Peyron, N.2
Nthen, M.3
Cichon, S.4
Drouet, C.5
-
16
-
-
33644896534
-
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men
-
K. Bork, D. Gl, G. Dewald Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men Br J Dermatol 154 2006 542 545
-
(2006)
Br J Dermatol
, vol.154
, pp. 542-545
-
-
Bork, K.1
Gl, D.2
Dewald, G.3
-
17
-
-
79958081751
-
Factor XII gene missense mutation Thr328Lys in an Arab family with hereditary angioedema type III
-
M.L. Baeza, A. Rodrguez-Marco, A. Prieto, J.M. Rodrguez-Sainz, Zubeldia, M. Rubio Factor XII gene missense mutation Thr328Lys in an Arab family with hereditary angioedema type III Allergy 66 2011 981 982
-
(2011)
Allergy
, vol.66
, pp. 981-982
-
-
Baeza, M.L.1
Rodrguez-Marco, A.2
Prieto, A.3
Rodrguez-Sainz Zubeldia, J.M.4
Rubio, M.5
-
18
-
-
35448963825
-
Hereditary angioedema with normal C1 inhibitor: Clinical symptoms and course
-
K. Bork, D. Gl, J. Hardt, G. Dewald Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course Am J Med 120 2007 987 992
-
(2007)
Am J Med
, vol.120
, pp. 987-992
-
-
Bork, K.1
Gl, D.2
Hardt, J.3
Dewald, G.4
-
20
-
-
42549088313
-
Oestrogen-dependent hereditary angio-oedema with normal C1 inhibitor: Description of six new cases and review of pathogenic mechanisms and treatment
-
C. Serrano, M. Guilarte, R. Tella Oestrogen-dependent hereditary angio-oedema with normal C1 inhibitor: description of six new cases and review of pathogenic mechanisms and treatment Allergy 63 2008 735 741
-
(2008)
Allergy
, vol.63
, pp. 735-741
-
-
Serrano, C.1
Guilarte, M.2
Tella, R.3
-
21
-
-
0035032184
-
Hereditary angioedema type III: An additional French pedigree with autosomal dominant transmission
-
L. Martin, D. Degenne, A. Toutain, D. Ponard, H. Watier Hereditary angioedema type III: an additional French pedigree with autosomal dominant transmission J Allergy Clin Immunol 107 2001 747 748
-
(2001)
J Allergy Clin Immunol
, vol.107
, pp. 747-748
-
-
Martin, L.1
Degenne, D.2
Toutain, A.3
Ponard, D.4
Watier, H.5
-
22
-
-
1242320163
-
Efficacy of danazol treatment in a patient with the new variant of hereditary angio-edema (HAE III)
-
G. Herrmann, L. Schneider, T. Krieg, N. Hunzelmann, K. Sharfetter-Kochanek Efficacy of danazol treatment in a patient with the new variant of hereditary angio-edema (HAE III) Br J Dermatol 150 2004 157 158
-
(2004)
Br J Dermatol
, vol.150
, pp. 157-158
-
-
Herrmann, G.1
Schneider, L.2
Krieg, T.3
Hunzelmann, N.4
Sharfetter-Kochanek, K.5
-
23
-
-
58649103742
-
Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III
-
A. Prieto, P. Tornero, M. Rubio, E. Fernndez-Cruz, C. Rodriguez-Sainz Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III Allergy 64 2009 284 286
-
(2009)
Allergy
, vol.64
, pp. 284-286
-
-
Prieto, A.1
Tornero, P.2
Rubio, M.3
Fernndez-Cruz, E.4
Rodriguez-Sainz, C.5
-
24
-
-
12244255797
-
Angioedema and oral contraception
-
L. Bouillet, D. Ponard, C. Drouet, D. Jullien, C. Massot Angioedema and oral contraception Dermatology 206 2003 106 109
-
(2003)
Dermatology
, vol.206
, pp. 106-109
-
-
Bouillet, L.1
Ponard, D.2
Drouet, C.3
Jullien, D.4
Massot, C.5
-
25
-
-
80053133424
-
Obstetrical complications and outcome in two families with hereditary angioedema due to mutation in the F12 gene
-
O. Picone, A.C. Donnadieu, F.G. Brivet, C. Boyer-Neumann, V. Frmeaux-Bacchi, R. Frydman Obstetrical complications and outcome in two families with hereditary angioedema due to mutation in the F12 gene Obstet Gynecol Int 957507 2010
-
(2010)
Obstet Gynecol Int
, pp. 957507
-
-
Picone, O.1
Donnadieu, A.C.2
Brivet, F.G.3
Boyer-Neumann, C.4
Frmeaux-Bacchi, V.5
Frydman, R.6
-
26
-
-
85056023763
-
A case of hereditary angio-oedema type III presenting with C 1-inhibitor cleavage and a missense mutation in the F 12 gene
-
L. Bouillet, D. Ponard, H. Rousset, S. Cichon, C. Drouet A case of hereditary angio-oedema type III presenting with C 1-inhibitor cleavage and a missense mutation in the F 12 gene Br J Dermatol 156 2007 1045 1092
-
(2007)
Br J Dermatol
, vol.156
, pp. 1045-1092
-
-
Bouillet, L.1
Ponard, D.2
Rousset, H.3
Cichon, S.4
Drouet, C.5
-
27
-
-
73349110107
-
Bradykinin receptor 2 antagonist (icatibant) for hereditary angioedema type III attacks
-
L. Bouillet, I. Boccon-Gibod, D. Ponard Bradykinin receptor 2 antagonist (icatibant) for hereditary angioedema type III attacks Ann Allergy Asthma Immunol 103 2009 448
-
(2009)
Ann Allergy Asthma Immunol
, vol.103
, pp. 448
-
-
Bouillet, L.1
Boccon-Gibod, I.2
Ponard, D.3
-
28
-
-
84355162896
-
Treatment of an acute attack of type III hereditary angioedema with ecallantide
-
J.A. Cronin, K.M. Maples Treatment of an acute attack of type III hereditary angioedema with ecallantide Ann Allergy Asthma Immunol 108 2012 61 62
-
(2012)
Ann Allergy Asthma Immunol
, vol.108
, pp. 61-62
-
-
Cronin, J.A.1
Maples, K.M.2
|