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Items: 1 to 20 of 129

1.

Hereditary angioedema: report of a large kindred with a rare genetic variant of C1-esterase inhibitor.

De Marchi M, Jacot-Guillarmod H, Ressa TG, Carbonara AO.

Clin Genet. 1973;4(3):229-36. No abstract available.

PMID:
4128807
2.

Hereditary angioedema. Report of a large kindred with a rare genetic variant of C1-esterase inhibitor.

Jacot-Guillarmod H, Carbonara AO, De Marchi M, Ressa TG.

Quad Sclavo Diagn. 1973 Mar;9(1):159-65. No abstract available.

PMID:
4132954
3.

[Studies on complement factors in hereditary Quincke's edema].

Kueppers F, Schulz KH.

Arch Dermatol Forsch. 1972;244:560-2. German. No abstract available.

PMID:
4648771
4.
5.

Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema.

Rosen FS, Alper CA, Pensky J, Klemperer MR, Donaldson VH.

J Clin Invest. 1971 Oct;50(10):2143-9.

6.
7.

Inherited high serum levels of a functionally deficient complement esterase inhibitor associated with hereditary angioedema.

Kueppers F, Berendes U, Schöpf E.

Humangenetik. 1972;15(2):119-25. No abstract available.

PMID:
4626030
8.

The genetics of hereditary angioedema: a hypothesis.

Shokeir MH.

Clin Genet. 1973 Jun;4(6):494-9. No abstract available.

PMID:
4207178
9.
10.

[Determination of the C1 esterase inhibitor].

Brécy H, Hartmann L.

Ann Biol Clin (Paris). 1971;29(5):397-401. French. No abstract available.

PMID:
5145640
11.

[Determination of inhibitor of the first component of complement (C1 INH) in patients with hereditary angioedema].

Rivero S, Gajardo M, Guzmán L.

Rev Med Chil. 1982 May;110(5):444-8. Spanish. No abstract available.

PMID:
6819622
12.

Hereditary angioneurotic edema (HANE): Lack of close linkage between HLA haplotypes and C1 esterase inhibitor deficiency.

Ohela K, Tiilikainen A, Kaakinen A, Räsänen J.

Tissue Antigens. 1977 Feb;9(2):90-5.

PMID:
841567
13.

Immunodiffusion assay of C1 inhibitor function in serum: prospective analysis in angioedema-urticaria.

Yelvington M, Prograis LJ Jr, Pizzo CJ, Curd JG.

Am J Clin Pathol. 1983 Sep;80(3):309-13.

PMID:
6410904
14.

[A molecular disease: hereditary angioneurotic edema. Study of 16 families].

Hartmann L, Brécy H, Ollier MP, Rethore O.

Biomedicine. 1974 Jul;21(7):294-302. French. No abstract available.

PMID:
4215470
15.

Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.

Bork K, Gül D, Hardt J, Dewald G.

Am J Med. 2007 Nov;120(11):987-92.

PMID:
17976427
16.

Studies on purified C'1 esterase and hereditary angioneurotic oedema sera by combined electrophoresis and immune haemolysis.

Siboo R, Laurell AB.

Acta Pathol Microbiol Scand. 1965;65(3):413-20. No abstract available.

PMID:
4160934
17.

Hereditary angioneurotic oedema.

Calvert GD, Kilpatrick D, McQueen EG, Houston IB, Kilpatrick JA, Veale AM.

N Z Med J. 1973 Oct 24;78(501):337-42. No abstract available.

PMID:
4148632
18.

[Abdominal manifestations in hereditary acute angioneurotic oedema. Value of study of the complement system (author's transl)].

Moulias R, Brecy H, Ollier MP, Roualdes M, Maïza M, Hartmann L.

Nouv Presse Med. 1977 Jun 18;6(25):2233, 2235-8. French.

PMID:
896410
20.

[Hereditary angioedema: clinical and laboratory aspects of 7 cases].

Moschione-Castro AP, Croce J, Diogo CL, Jacob CM, Pastorino AC, Kirschfink M, Grumach AS.

Rev Hosp Clin Fac Med Sao Paulo. 1998 Jan-Feb;53(1):21-5. Portuguese.

PMID:
9659739

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