IngentaConnect Search Results

Sites of initial bleeding episodes, mode of delivery and age of diagnosis in babies with haemophilia diagnosed before the age of 2 years: a report from The Centers for Disease Control and Prevention's (CDC) Universal Data Collection (UDC) project

Authors: KULKARNI, R.; SOUCIE, J. M.; LUSHER, J.; PRESLEY, R.; SHAPIRO, A.; GILL, J.; MANCO-JOHNSON, M.; KOERPER, M.; MATHEW, P.; ABSHIRE, T.; DIMICHELE, D.; HOOTS, K.; JANCO, R.; NUGENT, D.; GERAGHTY, S.; EVATT, B.

Source: Haemophilia, Volume 15, Number 6, November 2009 , pp. 1281-1290(10)

Publisher: Blackwell Publishing

Profiling of factor VIII mutations in Korean haemophilia A

Authors: HWANG, S. H.; KIM, M. J.; LIM, J. A.; KIM, H. C.; KIM, H. S.

Source: Haemophilia, Volume 15, Number 6, November 2009 , pp. 1311-1317(7)

Publisher: Blackwell Publishing

Improved criterion-referenced assessment in indirect tracking of haemophilia A using a 0.23 cM-resolution dense polymorphic marker set

Authors: MACHADO, F. B.; DUARTE, L. P.; MEDINA-ACOSTA, E.

Source: Haemophilia, Volume 15, Number 5, September 2009 , pp. 1135-1142(8)

Publisher: Blackwell Publishing

Effects of the CCR5-Δ32 Mutation on Hepatitis C Virus-Specific Immune Responses in Patients with Haemophilia

Authors: Ahlenstiel, Golo; Woitas, Rainer; Iwan, Agathe; Nattermann, Jacob; Feldmann, Georg; Rockstroh, Jurgen; Oldenburg, Johannes; Kupfer, Bernd; Sauerbruch, Tilman; Spengler, Ulrich

Source: Immunological Investigations, Volume 38, Numbers 3-4, April 2009 , pp. 284-296(13)

Publisher: Informa Healthcare

Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency

Authors: LANNOY, N.; ABINET, I.; DAHAN, K.; HERMANS, C.

Source: Haemophilia, Volume 15, Number 3, May 2009 , pp. 797-801(5)

Publisher: Blackwell Publishing

Effects of the CCR5-Δ32 Mutation on Hepatitis C Virus-Specific Immune Responses in Patients with Haemophilia

Authors: Ahlenstiel, Golo; Woitas, Rainer; Iwan, Agathe; Nattermann, Jacob; Feldmann, Georg; Rockstroh, Jurgen; Oldenburg, Johannes; Kupfer, Bernd; Sauerbruch, Tilman; Spengler, Ulrich

Source: Immunological Investigations, Volume 38, Number 1, January 2009 , pp. 1-13(13)

Publisher: Informa Healthcare

Variability in bleeding phenotype in Amish carriers of haemophilia B with the 31008 C→T mutation

Authors: SHARATHKUMAR, A.; HARDESTY, B.; GREIST, A.; SALTER, J.; KERLIN, B.; HEIMAN, M.; SULKIN, M.; SHAPIRO, A.

Source: Haemophilia, Volume 15, Number 1, January 2009 , pp. 91-100(10)

Publisher: Blackwell Publishing

Diagnosis and treatment of inherited factor X deficiency

Authors: BROWN, D. L.; KOUIDES, P. A.

Source: Haemophilia, Volume 14, Number 6, November 2008 , pp. 1176-1182(7)

Publisher: Blackwell Publishing

Skewed X chromosome inactivation in fraternal female twins results in moderately severe and mild haemophilia B

Authors: OKUMURA, K.; FUJIMORI, Y.; TAKAGI, A.; MURATE, T.; OZEKI, M.; YAMAMOTO, K.; KATSUMI, A.; MATSUSHITA, T.; NAOE, T.; KOJIMA, T.

Source: Haemophilia, Volume 14, Number 5, September 2008 , pp. 1088-1093(6)

Publisher: Blackwell Publishing

Management of carriers and babies with haemophilia

Authors: STREET, A. M.; LJUNG, R.; LAVERY, S. A.

Source: Haemophilia, Volume 14, Supplement 3, July 2008 , pp. 181-187(7)

Publisher: Blackwell Publishing

Carrier testing in haemophilia A and B: adult carriers' and their partners' experiences and their views on the testing of young females

Authors: DUNN, N. F.; MILLER, R.; GRIFFIOEN, A.; LEE, C. A.

Source: Haemophilia, Volume 14, Number 3, May 2008 , pp. 584-592(9)

Publisher: Blackwell Publishing

Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers

Authors: BUSTAMANTE-ARAGONES, A.; RODRIGUEZ DE ALBA, M.; GONZALEZ-GONZALEZ, C.; TRUJILLO-TIEBAS, M. J.; DIEGO-ALVAREZ, D.; VALLESPIN, E.; PLAZA, J.; AYUSO, C.; RAMOS, C.

Source: Haemophilia, Volume 14, Number 3, May 2008 , pp. 593-598(6)

Publisher: Blackwell Publishing

Heterozygous large deletions of Factor 8 gene in females identified by multiplex PCR-LC

Authors: PAVLOVA, A.; FÖRSTER, T.; DELEV, D.; SCHRÖDER, J.; EL-MAARRI, O.; MÜLLER-REIBLE, C.; OLDENBURG, J.

Source: Haemophilia, Volume 14, Number 3, May 2008 , pp. 599-606(8)

Publisher: Blackwell Publishing

A web-based registry of inherited bleeding disorders in the region of Emilia-Romagna: results at three and a half years

Authors: TAGLIAFERRI, A.; RIVOLTA, G. F.; BIASOLI, C.; VALDRÉ, L.; RODORIGO, G.; D'INCÁ, M.; MORATELLI, S.; ALBERTINI, P.; VINCENZI, D.; ARBASI, M. C.; MARIETTA, M.; PATTACINI, C.

Source: Haemophilia, Volume 14, Number 2, March 2008 , pp. 343-354(12)

Publisher: Blackwell Publishing

Management of menorrhagia in women with inherited bleeding disorders: general principles and use of desmopressin

Author: RODEGHIERO, F.

Source: Haemophilia, Volume 14, Supplement 1, January 2008 , pp. 21-30(10)

Publisher: Blackwell Publishing

Pregnancy in carriers of haemophilia

Authors: CHI, C.; LEE, C. A.; SHILTAGH, N.; KHAN, A.; POLLARD, D.; KADIR, R. A.

Source: Haemophilia, Volume 14, Number 1, January 2008 , pp. 56-64(9)

Publisher: Blackwell Publishing

Analysing two dinucleotide repeats of FVIII gene in Iranian population

Authors: RABBANI, B.; REZAEIAN, A.; KHANAHMAD, H.; BAGHERI, R.; KAMALI, E.; ZEINALI, S.