These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. [Two cases of parahemophilia due to deficiency of Owren's factors V and VII]. LOPEZ-BOTET E; VILAR R Rev Clin Esp; 1955 Aug; 58(4):220-4. PubMed ID: 13281046 [No Abstract] [Full Text] [Related]
4. Parahemophilia in three siblings (Owren's disease). ALEXANDER B; GOLDSTEIN R Am J Med; 1952 Sep; 13(3):255-72. PubMed ID: 12985584 [No Abstract] [Full Text] [Related]
5. [Congenital deficiency of proaccelerin (Owren's parahemophilia). Clinical and physiopathological observations]. GOBBI F; ASCARI E; BARBIERI U Minerva Med; 1960 Jan; 51():78-87. PubMed ID: 13850319 [No Abstract] [Full Text] [Related]
6. Parahemophilia (Owren's disease); report of a case in a woman with studies on other members of her family. STOHLMAN F; HARRINGTON WJ; MOLONEY WC J Lab Clin Med; 1951 Dec; 38(6):842-5. PubMed ID: 14889071 [No Abstract] [Full Text] [Related]
7. A hemorrhagic diathesis due to proaccelerin deficiency (congenital parahemophilia); a case report. FAETH WH Conn State Med J; 1953 Aug; 17(8):664-6. PubMed ID: 13067613 [No Abstract] [Full Text] [Related]
10. Parahaemophilia; haemorrhagic diathesis due to absence of a previously unknown clotting factor. OWREN PA Lancet; 1947 Apr; 1(6449):446-8. PubMed ID: 20293060 [No Abstract] [Full Text] [Related]
11. [Major proaccelerin (factor V) deficiency of congenital origin: "Owren's disease"]. Saint-Paul B; Chassaigne M Gaz Med Fr; 1966 Feb; 73(4):707-16. PubMed ID: 5904260 [No Abstract] [Full Text] [Related]
12. [OWREN'S DISEASE OR PARAHEMOPHILIA. REVIEW OF THE PUBLISHED CASES AND A PERSONAL CONTRIBUTION]. CENTURELLI G Rass Fisiopatol Clin Ter; 1963; 35():451-88. PubMed ID: 14069192 [No Abstract] [Full Text] [Related]
15. Haemorrhagic diathesis in children associated with vitamin K deficiency. Taj-Eldin S; al-Nouri L; Fakri O J Clin Pathol; 1967 May; 20(3):252-6. PubMed ID: 5602558 [TBL] [Abstract][Full Text] [Related]
16. [OWREN'S DISEASES (CONGENITAL FACTOR V DEFICIENCY, PARAHEMOPHILIA) IN TWO NEGRO SISTERS]. RETIEF FP; COETZEE PJ S Afr Med J; 1964 Jul; 38():544-7. PubMed ID: 14176707 [No Abstract] [Full Text] [Related]
17. Congenital and familial hypoconvertinemias; synoptic review of literature and a presentation of a personal case sensible to vitamin K. AVOGARO P Acta Med Patav; 1956; 16(1):1-40. PubMed ID: 13339126 [No Abstract] [Full Text] [Related]
18. [Rational diagnosis of hemorrhagic diathesis as a basis for quick therapeutic treatment]. Remde W Z Arztl Fortbild (Jena); 1966 Sep; 60(17):1002-6. PubMed ID: 5995284 [No Abstract] [Full Text] [Related]
19. Factor 5 deficiency in hemorrhagic diathesis (parahemophilia). COSGRIFF SW; LEIFER E J Am Med Assoc; 1952 Feb; 148(6):462-3. PubMed ID: 14888507 [No Abstract] [Full Text] [Related]
20. Hemorrhagic diathesis during pregnancy due to unexplained lack of vitamin K. A case report. LARSEN RA Acta Med Scand; 1960 Jul; 167():171-5. PubMed ID: 14414280 [No Abstract] [Full Text] [Related] [Next] [New Search]