148 related articles for article (PubMed ID: 37132158)
1. The impact of concurrent X chromosome anomalies on diagnosis and bleeding phenotype in children with hemophilia: A single-institution case series.
Soffer E; Coleman K; Batsuli G
Pediatr Blood Cancer; 2023 Jul; 70(7):e30400. PubMed ID: 37132158
[TBL] [Abstract][Full Text] [Related]
2. Severe haemophilia A in a preterm girl with Turner syndrome: case report - a diagnostic and therapeutic challenge for a paediatrician (Part 2).
Agnieszka B; Monika WM; Barbara W; Anna K
Ital J Pediatr; 2021 Jul; 47(1):157. PubMed ID: 34256805
[TBL] [Abstract][Full Text] [Related]
3. Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report.
Al Khudari R; Batesh D; Habash R; Hamdn O
J Med Case Rep; 2023 Nov; 17(1):480. PubMed ID: 37978530
[TBL] [Abstract][Full Text] [Related]
4. Hemophilia with factor VIII and factor IX inhibitors, incidence, bleeding problems and management.
Mahasandana C; Patharathienskul D; Suvatte V
Southeast Asian J Trop Med Public Health; 1993; 24 Suppl 1():106-12. PubMed ID: 7886549
[TBL] [Abstract][Full Text] [Related]
5. X Chromosome inactivation: a modifier of factor VIII and IX plasma levels and bleeding phenotype in Haemophilia carriers.
Garagiola I; Mortarino M; Siboni SM; Boscarino M; Mancuso ME; Biganzoli M; Santagostino E; Peyvandi F
Eur J Hum Genet; 2021 Feb; 29(2):241-249. PubMed ID: 33082527
[TBL] [Abstract][Full Text] [Related]
6. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B.
Orstavik KH; Scheibel E; Ingerslev J; Schwartz M
Thromb Haemost; 2000 Mar; 83(3):433-7. PubMed ID: 10744150
[TBL] [Abstract][Full Text] [Related]
7. Intracranial hemorrhage in a female leading to the diagnosis of severe hemophilia A and Turner syndrome.
Weinspach S; Siepermann M; Schaper J; Sarikaya-Seiwert S; Rieder H; Gerigk M; Höhn T; Laws HJ
Klin Padiatr; 2009; 221(3):167-71. PubMed ID: 19437365
[TBL] [Abstract][Full Text] [Related]
8. Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52.
Panarello C; Acquila M; Caprino D; Gimelli G; Pecorara M; Mori PG
Cytogenet Cell Genet; 1992; 59(4):241-2. PubMed ID: 1544315
[TBL] [Abstract][Full Text] [Related]
9. Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients-Lessons from Wide Genome Analyses.
Dardik R; Avishai E; Lalezari S; Barg AA; Levy-Mendelovich S; Budnik I; Barel O; Khavkin Y; Kenet G; Livnat T
Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445777
[TBL] [Abstract][Full Text] [Related]
10. A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes.
Gilgenkrantz S; Briquel ME; Mandel JL; Oberle I
Hum Genet; 1986 Feb; 72(2):157-9. PubMed ID: 3455922
[TBL] [Abstract][Full Text] [Related]
11. Inhibitor antibodies to factor VIII and factor IX: management.
Lusher JM
Semin Thromb Hemost; 2000; 26(2):179-88. PubMed ID: 10919411
[TBL] [Abstract][Full Text] [Related]
12. Severe haemophilia a in a preterm girl with turner syndrome - a case report from the prenatal period to early infancy (part I).
Berendt A; Wójtowicz-Marzec M; Wysokińska B; Kwaśniewska A
Ital J Pediatr; 2020 Sep; 46(1):125. PubMed ID: 32894158
[TBL] [Abstract][Full Text] [Related]
13. Treatment of considerations in patients with compartment syndrome and an inherited bleeding disorder.
Naranja RJ; Chan PS; High K; Esterhai JL; Heppenstall RB
Orthopedics; 1997 Aug; 20(8):706-9; quiz 710-1. PubMed ID: 9263290
[TBL] [Abstract][Full Text] [Related]
14. Severe hemophilia in a girl infant with mosaic Turner syndrome and persistent hyperplastic primary vitreous.
Shahriari M; Bazrafshan A; Moghadam M; Karimi M
Blood Coagul Fibrinolysis; 2016 Apr; 27(3):352-3. PubMed ID: 26484646
[TBL] [Abstract][Full Text] [Related]
15. Acquired Hemophilia A: A Case Report.
Shen M; Wang S; Sessa J; Hanna A; Axelrad A; Ali F
J Pharm Pract; 2020 Aug; 33(4):562-566. PubMed ID: 30727803
[TBL] [Abstract][Full Text] [Related]
16. Regulation and importance of factor VIII levels in hemophilia A carriers.
Cygan PH; Kouides PA
Curr Opin Hematol; 2021 Sep; 28(5):315-322. PubMed ID: 34397591
[TBL] [Abstract][Full Text] [Related]
17. Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndrome.
Chuansumrit A; Sasanakul W; Goodeve A; Treratvirapong T; Parinayok R; Pintadit P; Hathirat P
Thromb Haemost; 1999 Oct; 82(4):1379. PubMed ID: 10544944
[No Abstract] [Full Text] [Related]
18. Manifestations of factor VIII inhibitor in the head and neck.
DellaCroce FJ; Kountakis S; Aguilar EF
Arch Otolaryngol Head Neck Surg; 1999 Nov; 125(11):1258-61. PubMed ID: 10555699
[TBL] [Abstract][Full Text] [Related]
19. Results of secondary prophylaxis in children with severe hemophilia.
Manco-Johnson MJ; Nuss R; Geraghty S; Funk S; Kilcoyne R
Am J Hematol; 1994 Oct; 47(2):113-7. PubMed ID: 8092125
[TBL] [Abstract][Full Text] [Related]
20. Hemophilia A and C in a female: The first case report in literature.
Alkarrash MS; Badawi R; Sallah H; Shashaa MN; Argilo J; Alkhoury R
Ann Med Surg (Lond); 2021 Aug; 68():102561. PubMed ID: 34336195
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
