Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören-Pürsün, E
Binkley, K.E
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A.J
Cicardi, M
Davis III, A.E
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Fontana, L
Füst, G
Giacomelli, R
Gröner, A
Erik Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P.N
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H.J
Lopez-Trascasa, M
Martinez-Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E.W
Nuijens, J.H
O'Grady, C
Pappalardo, E
Penna, V
Perricone, C
Perricone, R
Rauch, U
Roche, O
Rusicke, E
Späth, P.J
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L

January 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören Pürsün, E
Binkley, K
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A
Cicardi, M
Davis, A
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Füst, G
Giacomelli, R
Gröner, A
Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H
Lopez Trascasa, M
Martinez Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E
Nuijens, J
O'grady, C
Pappalardo, E
Penna, V
Perricone, C
Rauch, U
Roche, O
Rusicke, E
Späth, P
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L.
FONTANA, LUIGI
PERRICONE, ROBERTO

September 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Angioedema due to acquired C1-inhibitor deficiency : a bridging condition between autoimmunity and lymphoproliferation

M. Cugno
M. Cicardi
R. Castelli

December 2008

Angioedema due to an acquired deficiency in the inhibitor of the first component of human complement...

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

Zanichelli, Andrea
Longhurst, Hilary J
Maurer, Marcus
Bouillet, Laurence
Aberer, Werner
Fabien, Vincent
Andresen, Irmgard
Caballero, Teresa
MARONE, GIANNI

January 2016

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...

Hereditary Angioedema: a Challenging Diagnosis for the Gastroenterologist

Gábos Gabriella
Moldovan Dumitru
Dobru Daniela

December 2016

Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...

Angioedema due to C1 inhibitor deficiency in 2010

M. Cicardi
A. Zanichelli

January 2010

Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increa...

The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures

Anna Valerieva
Marco Cicardi
James Baraniuk
Maria Staevska

October 2018

Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare auto...

Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)

N.T.M.L. Fragnan
A.L.N. Tolentino
G.B. Borba
A.C. Oliveira
J.A. Simões
S.M.U. Palma
R.N. Constantino-Silva
A.S. Grumach

November 2018

Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...

C1-inhibitor deficiency and angioedema

A. Carugati
E. Pappalardo
L.C. Zingale
M. Cicardi

January 2001

C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...

Hereditary angioedema with normal c1 inhibitor: Clinical symptoms and course

Bork, Konrad

A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...

Therapeutic management of hereditary angioedema due to C1 inhibitor deficiency

A. Zanichelli
M. Mansi
G. Periti
M. Cicardi

January 2013

Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...

Diagnostic and therapeutic management of hereditary angioedema due to C1-inhibitor deficiency: The Italian experience

Cancian M
Arcoleo F
Bafunno V
Barca MP
Borrelli P
Bova M
Di Rocco PC
Cicardi M
Cillari E
De Carolis C
De Pasquale T
Del Corso I
Guarino MD
Massaro I
Minale P
Montinaro V
Neri S
Perricone R
Pucci S
Quattrocchi P
Rossi O
Senter R
Zanichelli A
Zanierato G
Zoli A.
TRIGGIANI, MASSIMO

January 2015

Purpose of review Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) i...

Hereditary angio-oedema

Longhurst, Hilary
Cicardi, Marco

February 2012

SummaryHereditary angio-oedema is caused by a heterozygous deficiency of C1 inhibitor. This inhibito...

Hereditary and acquired angioedema : problems and progress : proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

A. Agostoni
E. Aygoren Pursun
K. E. Binkley
A. Blanch
K. Bork
L. Bouillet
C. Bucher
A. J. Castaldo
M. Cicardi
A. E. Davis
C. De Carolis
C. Drouet
C. Duponchel
H. Farkas
K. Fay
B. Fekete
B. Fischer
L. Fontana
G. Fust
R. Giacomelli
A. Groner
C. E. Hack
G. Harmat
J. Jakenfelds
M. Juers
L. Kalmar
P. N. Kaposi
I. Karadi
A. Kitzinger
T. Kollar
W. Kreuz
P. Lakatos
H. J. Longhurst
M. Lopez Trascasa
I. Martinez Saguer
N. Monnier
I. Nagy
E. Nemeth
E. W. Nielsen
J. H. Nuijens
C. O'Grady
E. Pappalardo
V. Penna
C. Perricone
R. Perricone
U. Rauch
O. Roche
E. Rusicke
P. J. Spath
G. Szendei
E. Takacs
A. Tordai
L. Truedsson
L. Varga
B. Visy
K. Williams
A. Zanichelli
L. Zingale

September 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Hereditary angioedema: Complex symptoms can make diagnosis difficult

Borum, Marie L.
Howard, Dominique E.

January 1998

Hereditary angioedema is a rare disorder characterized by a deficiency in C1 esterase inhibitor. Sym...

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören-Pürsün, E
Binkley, K.E
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A.J
Cicardi, M
Davis III, A.E
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Fontana, L
Füst, G
Giacomelli, R
Gröner, A
Erik Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P.N
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H.J
Lopez-Trascasa, M
Martinez-Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E.W
Nuijens, J.H
O'Grady, C
Pappalardo, E
Penna, V
Perricone, C
Perricone, R
Rauch, U
Roche, O
Rusicke, E
Späth, P.J
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L

January 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören Pürsün, E
Binkley, K
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A
Cicardi, M
Davis, A
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Füst, G
Giacomelli, R
Gröner, A
Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H
Lopez Trascasa, M
Martinez Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E
Nuijens, J
O'grady, C
Pappalardo, E
Penna, V
Perricone, C
Rauch, U
Roche, O
Rusicke, E
Späth, P
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L.
FONTANA, LUIGI
PERRICONE, ROBERTO

September 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Angioedema due to acquired C1-inhibitor deficiency : a bridging condition between autoimmunity and lymphoproliferation

M. Cugno
M. Cicardi
R. Castelli

December 2008

Angioedema due to an acquired deficiency in the inhibitor of the first component of human complement...

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

Zanichelli, Andrea
Longhurst, Hilary J
Maurer, Marcus
Bouillet, Laurence
Aberer, Werner
Fabien, Vincent
Andresen, Irmgard
Caballero, Teresa
MARONE, GIANNI

January 2016

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...

Hereditary Angioedema: a Challenging Diagnosis for the Gastroenterologist

Gábos Gabriella
Moldovan Dumitru
Dobru Daniela

December 2016

Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...

Angioedema due to C1 inhibitor deficiency in 2010

M. Cicardi
A. Zanichelli

January 2010

Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increa...

The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures

Anna Valerieva
Marco Cicardi
James Baraniuk
Maria Staevska

October 2018

Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare auto...

Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases)

N.T.M.L. Fragnan
A.L.N. Tolentino
G.B. Borba
A.C. Oliveira
J.A. Simões
S.M.U. Palma
R.N. Constantino-Silva
A.S. Grumach

November 2018

Hereditary angioedema (HAE) is a rare autosomal dominant disease due to C1 esterase inhibitor defici...

C1-inhibitor deficiency and angioedema

A. Carugati
E. Pappalardo
L.C. Zingale
M. Cicardi

January 2001

C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...

Hereditary angioedema with normal c1 inhibitor: Clinical symptoms and course

Bork, Konrad

A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...

Therapeutic management of hereditary angioedema due to C1 inhibitor deficiency

A. Zanichelli
M. Mansi
G. Periti
M. Cicardi

January 2013

Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease charac...

Diagnostic and therapeutic management of hereditary angioedema due to C1-inhibitor deficiency: The Italian experience

Cancian M
Arcoleo F
Bafunno V
Barca MP
Borrelli P
Bova M
Di Rocco PC
Cicardi M
Cillari E
De Carolis C
De Pasquale T
Del Corso I
Guarino MD
Massaro I
Minale P
Montinaro V
Neri S
Perricone R
Pucci S
Quattrocchi P
Rossi O
Senter R
Zanichelli A
Zanierato G
Zoli A.
TRIGGIANI, MASSIMO

January 2015

Purpose of review Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) i...

Hereditary angio-oedema

Longhurst, Hilary
Cicardi, Marco

February 2012

SummaryHereditary angio-oedema is caused by a heterozygous deficiency of C1 inhibitor. This inhibito...

Hereditary and acquired angioedema : problems and progress : proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

A. Agostoni
E. Aygoren Pursun
K. E. Binkley
A. Blanch
K. Bork
L. Bouillet
C. Bucher
A. J. Castaldo
M. Cicardi
A. E. Davis
C. De Carolis
C. Drouet
C. Duponchel
H. Farkas
K. Fay
B. Fekete
B. Fischer
L. Fontana
G. Fust
R. Giacomelli
A. Groner
C. E. Hack
G. Harmat
J. Jakenfelds
M. Juers
L. Kalmar
P. N. Kaposi
I. Karadi
A. Kitzinger
T. Kollar
W. Kreuz
P. Lakatos
H. J. Longhurst
M. Lopez Trascasa
I. Martinez Saguer
N. Monnier
I. Nagy
E. Nemeth
E. W. Nielsen
J. H. Nuijens
C. O'Grady
E. Pappalardo
V. Penna
C. Perricone
R. Perricone
U. Rauch
O. Roche
E. Rusicke
P. J. Spath
G. Szendei
E. Takacs
A. Tordai
L. Truedsson
L. Varga
B. Visy
K. Williams
A. Zanichelli
L. Zingale

September 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Hereditary angioedema: Complex symptoms can make diagnosis difficult

Borum, Marie L.
Howard, Dominique E.

January 1998

Hereditary angioedema is a rare disorder characterized by a deficiency in C1 esterase inhibitor. Sym...

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören-Pürsün, E
Binkley, K.E
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A.J
Cicardi, M
Davis III, A.E
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Fontana, L
Füst, G
Giacomelli, R
Gröner, A
Erik Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P.N
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H.J
Lopez-Trascasa, M
Martinez-Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E.W
Nuijens, J.H
O'Grady, C
Pappalardo, E
Penna, V
Perricone, C
Perricone, R
Rauch, U
Roche, O
Rusicke, E
Späth, P.J
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L

January 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

Agostoni, A
Aygören Pürsün, E
Binkley, K
Blanch, A
Bork, K
Bouillet, L
Bucher, C
Castaldo, A
Cicardi, M
Davis, A
De Carolis, C
Drouet, C
Duponchel, C
Farkas, H
Fáy, K
Fekete, B
Fischer, B
Füst, G
Giacomelli, R
Gröner, A
Hack, C
Harmat, G
Jakenfelds, J
Juers, M
Kalmár, L
Kaposi, P
Karádi, I
Kitzinger, A
Kollár, T
Kreuz, W
Lakatos, P
Longhurst, H
Lopez Trascasa, M
Martinez Saguer, I
Monnier, N
Nagy, I
Németh, E
Nielsen, E
Nuijens, J
O'grady, C
Pappalardo, E
Penna, V
Perricone, C
Rauch, U
Roche, O
Rusicke, E
Späth, P
Szendei, G
Takács, E
Tordai, A
Truedsson, L
Varga, L
Visy, B
Williams, K
Zanichelli, A
Zingale, L.
FONTANA, LUIGI
PERRICONE, ROBERTO

September 2004

Hereditary angioedema (HAE), a rare but life-threatening condition, manifests as acute attacks of fa...

Angioedema due to acquired C1-inhibitor deficiency : a bridging condition between autoimmunity and lymphoproliferation

M. Cugno
M. Cicardi
R. Castelli

December 2008

Angioedema due to an acquired deficiency in the inhibitor of the first component of human complement...

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

Abstract

Extracted data

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting

Abstract

Extracted data

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