(Q33986895)

30 July 2017

title

Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain (English)

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30 July 2017

main subject

hereditary angioedema

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inferred from title

C1 inhibitor deficiency

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Olga Roche

1

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30 July 2017

Alvaro Blanch

2

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30 July 2017

Teresa Caballero

3

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30 July 2017

Noelia Sastre

4

1 reference

30 July 2017

Daniel Callejo

5

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30 July 2017

Margarita López-Trascasa

6

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30 July 2017

publication date

1 April 2005

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Annals of Allergy, Asthma & Immunology

30 July 2017

published in

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30 July 2017

volume

94

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30 July 2017

issue

4

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30 July 2017

page(s)

498-503

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Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Molecular genetics of C1 inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedema

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Hereditary angioedema with normal C1-inhibitor activity in women

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Hereditary angioedema

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Primary immunodeficiency diseases in Norway

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema.

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

How do we treat patients with hereditary angioedema

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Primary immunodeficiency syndrome in Spain: first report of the National Registry in Children and Adults

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

The Spanish Registry of Primary Immunodeficiencies (REDIP)

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Misdiagnosis of hereditary angio-oedema type 1 and type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

Long-term prophylaxis with C1-inhibitor (C1 INH) concentrate in patients with recurrent angioedema caused by hereditary and acquired C1-inhibitor deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2961121-0

7 January 2021

10.1016/S1081-1206(10)61121-0

Identifiers

DOI

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30 July 2017

1 reference