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Items: 1 to 20 of 110

1.

Hageman trait (factor XII deficiency): a probably second genotype inherited as an autosomal dominant characteristic.

Bennett B, Ratnoff OD, Holt JB, Roberts HR.

Blood. 1972 Sep;40(3):412-5. No abstract available.

2.

[Familial study in congenital Hageman factor deficiency (blood coagulation factor XII)].

Baumann R, Straub PW.

Schweiz Med Wochenschr. 1968 Oct 19;98(42):1653-5. German. No abstract available.

PMID:
5698343
3.

A new family with congenital factor XII deficiency.

Barbui T, Dini E.

Acta Haematol. 1975;54(6):345-9.

PMID:
812321
4.

Congenital deficiency of Hageman factor (clotting factor XII). Report on the first two families found in Switzerland.

Baumann R, Straub PW.

Helv Med Acta. 1968 Nov;34(4):313-26. No abstract available.

PMID:
5704616
5.
6.

[Study of a family with factor XII deficiency].

Licenziati M, Lazzari R, Falsina A.

Minerva Med. 1975 Feb 14;66(11):511-3. Italian. No abstract available.

PMID:
234603
7.

Hageman factor deficiency. Report of a case found in a Japanese girl.

Miwa S, Asai I, Tsukada T, Shimizu M, Teramura K, Sunaga Y.

Acta Haematol. 1968;39(1):36-41. No abstract available.

PMID:
4968868
8.

A case of Hageman factor deficiency with myeloid leukaemia.

McGrath K, Koutts J.

Aust N Z J Med. 1975 Apr;5(2):155-7.

PMID:
1057927
9.

Thromboembolism in Hageman trait.

McPherson RA.

Am J Clin Pathol. 1977 Sep;68(3):420-3.

PMID:
900075
10.

Hageman trait. The first case in Hungary (brief report).

Elödi S, Mód A, Poros A.

Haematologia (Budap). 1971;5(4):459-60. No abstract available.

PMID:
5148970
11.

Factor XII defect and hemorrhage. Evidence for a new type of hereditary hemostatic disorder.

Egeberg O.

Thromb Diath Haemorrh. 1970 Jun 30;23(3):432-40. No abstract available.

PMID:
5432188
12.

Immunologic demonstration of a deficiency of Hageman factor-like material in Hageman trait.

Smink MM, Daniel TM, Ratnoff OD, Stavitsky AB.

J Lab Clin Med. 1967 May;69(5):819-32. No abstract available.

PMID:
4960805
13.

[Hageman factor deficiency: second case found in Japanese].

Miwa S, Asai I, Tsukada T, Shimizu M, Teramura K.

Nihon Ketsueki Gakkai Zasshi. 1967 Nov;30(6):859-63. Japanese. No abstract available.

PMID:
5627222
14.

Rare congenital coagulation factor defects in Finland.

Ikkala E, Myllylä G, Nevanlinna HR.

Scand J Haematol. 1971;8(3):210-5. No abstract available.

PMID:
5093998
15.

[Factor XII deficiency in two brothers].

Müller G, Hilgard P, Hiemeyer V.

Dtsch Med Wochenschr. 1973 Feb 9;98(6):267-9. German. No abstract available.

PMID:
4684650
16.

[DURATION OF LIFE OF THE HAGEMAN FACTOR (FACTOR XII)].

JOSSO F, PROU-WARTELLE O, CHARLAS J.

Nouv Rev Fr Hematol. 1964 May-Jun;4:454-6. French. No abstract available.

PMID:
14186229
17.

Brief recordings. Rheumatoid arthritis in a patient with Hageman trait.

Donaldson VH, Glueck HI, Fleming T.

N Engl J Med. 1972 Mar 9;286(10):528-30. No abstract available.

PMID:
5059265
18.

Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme.

Bernardi F, Marchetti G, Patracchini P, del Senno L, Tripodi M, Fantoni A, Bartolai S, Vannini F, Felloni L, Rossi L, et al.

Blood. 1987 May;69(5):1421-4.

19.
20.

[Hageman factor deficiency. Apropos of a case].

Aznar J, Mayans J, Aznar JA, Fernández-Pavón A, Calabuig R.

Sangre (Barc). 1973;18(3):356-64. Spanish. No abstract available.

PMID:
4757644

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