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Results: 1 to 20 of 155

1.

Acute cerebrovascular accident in an 18-year-old male with von Willebrand disease.

Novick A, McGrann S, Lamfers R.

S D Med. 2014 May;67(5):191, 193, 195.

PMID:
24851466
[PubMed - indexed for MEDLINE]
2.

Thrombocytopathy and type 2B von Willebrand disease.

Ware J.

J Clin Invest. 2013 Dec 2;123(12):5004-6. doi: 10.1172/JCI73169. Epub 2013 Nov 25.

PMID:
24270415
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Committee Opinion No.580: von Willebrand disease in women.

Committee on Adolescent Health Care; Committee on Gynecologic Practice.

Obstet Gynecol. 2013 Dec;122(6):1368-73. doi: 10.1097/01.AOG.0000438961.38979.19.

PMID:
24264714
[PubMed - indexed for MEDLINE]
4.

Management of von Willebrand disease type 3 during pregnancy - 2 cases reports.

Inocêncio G, Braga A, Azevedo S, Buchner G.

Eur Rev Med Pharmacol Sci. 2013 Nov;17(21):2857-9.

PMID:
24254552
[PubMed - indexed for MEDLINE]
Free Article
5.

Inherited abnormalities of coagulation: hemophilia, von Willebrand disease, and beyond.

Kumar R, Carcao M.

Pediatr Clin North Am. 2013 Dec;60(6):1419-41. doi: 10.1016/j.pcl.2013.09.002. Review.

PMID:
24237980
[PubMed - indexed for MEDLINE]
6.

Spontaneous intramural duodenal hematoma in type 2B von Willebrand disease.

Eichele DD, Ross M, Tang P, Hutchins GF, Mailliard M.

World J Gastroenterol. 2013 Nov 7;19(41):7205-8. doi: 10.3748/wjg.v19.i41.7205.

PMID:
24222967
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Treating symptomatic coronary artery disease in patients with Von Willebrand disease.

Hassan SA, Amer S, Qureshi W, Alirhayim Z, Kuriakose P.

Hematol Oncol Stem Cell Ther. 2013 Sep-Dec;6(3-4):101-4. doi: 10.1016/j.hemonc.2013.08.004. Epub 2013 Oct 1.

PMID:
24096142
[PubMed - indexed for MEDLINE]
Free Article
8.

von Willebrand disease: advances in pathogenetic understanding, diagnosis, and therapy.

Lillicrap D.

Blood. 2013 Nov 28;122(23):3735-40. doi: 10.1182/blood-2013-06-498303. Epub 2013 Sep 24. Review.

PMID:
24065240
[PubMed - indexed for MEDLINE]
9.

Platelets and bleeding in the dental patient. It's not always from "blood thinners". Von Willebrand disease--clinical assessment and case report.

Cohen HV, Figueroa R, Quek SY, Abbas AM.

J N J Dent Assoc. 2013 Spring;84(2):28-30. No abstract available.

PMID:
23991505
[PubMed - indexed for MEDLINE]
10.

Platelet-type von Willebrand disease: new insights into the molecular pathophysiology of a unique platelet defect.

Othman M, Kaur H, Emsley J.

Semin Thromb Hemost. 2013 Sep;39(6):663-73. doi: 10.1055/s-0033-1353442. Epub 2013 Aug 11. Review.

PMID:
23934752
[PubMed - indexed for MEDLINE]
11.

Acquired von Willebrand disease in a child with a ventricular assist device.

Nubret K, Mauriat P, Roubertie F, James C, Tafer N, Ouattara A.

J Thorac Cardiovasc Surg. 2013 Oct;146(4):e30-2. doi: 10.1016/j.jtcvs.2013.06.023. Epub 2013 Jul 24. No abstract available.

PMID:
23891463
[PubMed - indexed for MEDLINE]
12.

Refractory bleeding from intestinal angiodysplasias successfully treated with danazol in three patients with von Willebrand disease.

Botero JP, Pruthi RK.

Blood Coagul Fibrinolysis. 2013 Dec;24(8):884-6. doi: 10.1097/MBC.0b013e3283646716.

PMID:
23867344
[PubMed - indexed for MEDLINE]
13.

Translational medicine advances in von Willebrand disease.

Lillicrap D.

J Thromb Haemost. 2013 Jun;11 Suppl 1:75-83. doi: 10.1111/jth.12257.

PMID:
23809112
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

New development in von Willebrand disease.

Castaman G.

Curr Opin Hematol. 2013 Sep;20(5):424-9. doi: 10.1097/MOH.0b013e328363c11f. Review.

PMID:
23852183
[PubMed - indexed for MEDLINE]
15.

The genetics of Canadian type 3 von Willebrand disease: further evidence for codominant inheritance of mutant alleles: a reply to a rebuttal.

Bowman M, Lillicrap D, James P.

J Thromb Haemost. 2013 Sep;11(9):1786-7. doi: 10.1111/jth.12348. No abstract available.

PMID:
23844668
[PubMed - indexed for MEDLINE]
16.

Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations.

Jokela V, Lassila R, Szanto T, Joutsi-Korhonen L, Armstrong E, Oyen F, Schneppenheim S, Schneppenheim R.

Haemophilia. 2013 Nov;19(6):e344-8. doi: 10.1111/hae.12225. Epub 2013 Jul 9.

PMID:
23834637
[PubMed - indexed for MEDLINE]
17.

The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal.

Kasatkar P, Ghosh K, Shetty S.

J Thromb Haemost. 2013 Sep;11(9):1784-5. doi: 10.1111/jth.12323. No abstract available.

PMID:
23773799
[PubMed - indexed for MEDLINE]
18.

Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.

Hampshire DJ, Abuzenadah AM, Cartwright A, Al-Shammari NS, Coyle RE, Eckert M, Al-Buhairan AM, Messenger SL, Budde U, Gürsel T, Ingerslev J, Peake IR, Goodeve AC.

Thromb Haemost. 2013 Aug;110(2):264-74. doi: 10.1160/TH13-02-0135. Epub 2013 May 23.

PMID:
23702511
[PubMed - indexed for MEDLINE]
19.

Posttonsillectomy hemorrhage in children with von Willebrand disease or hemophilia.

Sun GH, Auger KA, Aliu O, Patrick SW, DeMonner S, Davis MM.

JAMA Otolaryngol Head Neck Surg. 2013 Mar;139(3):245-9. doi: 10.1001/jamaoto.2013.1821.

PMID:
23657425
[PubMed - indexed for MEDLINE]
20.

Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient.

Enayat MS, Ravanbod S, Rassoulzadegan M, Jazebi M, Ala F, Budde U, Schneppenheim S, Obser T, Schneppenheim R.

Haemophilia. 2013 Jul;19(4):e261-4. doi: 10.1111/hae.12161. Epub 2013 May 7. No abstract available.

PMID:
23647747
[PubMed - indexed for MEDLINE]

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