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Similar articles for PubMed (Select 18081445)

1.

Bernard-Soulier syndrome: an inherited platelet disorder.

Pham A, Wang J.

Arch Pathol Lab Med. 2007 Dec;131(12):1834-6. Review.

PMID:
18081445
2.

Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib.

Devine DV, Currie MS, Rosse WF, Greenberg CS.

Blood. 1987 Aug;70(2):428-31.

3.

Variant Bernard-Soulier syndrome type bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex.

De Marco L, Mazzucato M, Fabris F, De Roia D, Coser P, Girolami A, Vicente V, Ruggeri ZM.

J Clin Invest. 1990 Jul;86(1):25-31.

4.

[Bernard-Soulier thrombocytopenia: clinical significance of a rare disorder].

Gengenbacher D, Tsakiris DA, Tichelli A, Marbet GA, Gratwohl A, Speck B.

Schweiz Med Wochenschr. 1996 Oct 26;126(43):1834-41. German.

PMID:
9005523
5.

Course of pregnancy and birth in a patient with Bernard-Soulier syndrome--a case report.

Rahimi G, Rellecke S, Mallmann P, Nawroth F.

J Perinat Med. 2005;33(3):264-6.

PMID:
15914354
6.

[Bernard-Soulier syndrome. An important differential diagnosis in chronic thrombocytopenia with bleeding complications].

Greinacher A, Zellner A, Brangenberg R, Kiefel V, Mueller-Eckhardt C.

Monatsschr Kinderheilkd. 1993 Jun;141(6):483-6. German.

PMID:
8336744
7.
8.

Bernard-Soulier syndrome.

Berndt MC, Fournier DJ, Castaldi PA.

Baillieres Clin Haematol. 1989 Jul;2(3):585-607. Review.

PMID:
2550101
9.

Bernard-Soulier syndrome (hemorrhagiparous thrombocytic dystrophy).

Lanza F.

Orphanet J Rare Dis. 2006 Nov 16;1:46. Review.

10.

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets.

Loffredo G, Baronciani L, Noris P, Menna F, Federici AB, Balduini CL.

Platelets. 2006 May;17(3):149-52.

PMID:
16702040
11.

[Bernard-Soulier syndrome in a Swiss family].

de Moerloose P, Vogel JJ, Clemetson KJ, Petite J, Bienz D, Bouvier CA.

Schweiz Med Wochenschr. 1987 Nov 14;117(46):1817-21. French.

PMID:
3423769
12.

[Bernard-Soulier syndrome revealed by major neonatal thrombocytopenia].

Pinto da Costa N, Armari-Alla C, Plantaz D, Pagnier A.

Arch Pediatr. 2003 Nov;10(11):983-5. French.

PMID:
14613692
13.

Bernard-Soulier syndrome: a new platelet glycoprotein abnormality. Its relationship with platelet adhesion to subendothelium and with the factor VIII von Willebrand protein.

Caen JP, Nurden AT, Jeanneau C, Michel H, Tobelem G, Levy-Toledano S, Sultan Y, Valensi F, Bernard J.

J Lab Clin Med. 1976 Apr;87(4):586-96.

PMID:
1083883
14.

Inherited bleeding disorders.

Blanchette VS, Sparling C, Turner C.

Baillieres Clin Haematol. 1991 Apr;4(2):291-332. Review.

PMID:
1912663
15.

Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.

Ghosh K, Nair S, Kulkarni B, Khare A, Shetty S, Mohanty D.

Platelets. 2003 Sep;14(6):351-4.

PMID:
14602548
16.

Bernard-Soulier syndrome in a Turkish family.

Okan V, Araz M, Camci C, Aktaran S, Sahin A, Buyukberber S, Bakir K, Cakmak EA.

Int J Clin Pract. 2002 Sep;56(7):546-8.

PMID:
12296619
17.

A three-base deletion removing a leucine residue in a leucine-rich repeat of platelet glycoprotein Ib alpha associated with a variant of Bernard-Soulier syndrome (Nancy I).

de la Salle C, Baas MJ, Lanza F, Schwartz A, Hanau D, Chevalier J, Gachet C, Briquel ME, Cazenave JP.

Br J Haematol. 1995 Feb;89(2):386-96.

PMID:
7873390
18.

An acquired Bernard-Soulier-like platelet defect associated with juvenile myelodysplastic syndrome.

Berndt MC, Kabral A, Grimsley P, Watson N, Robertson TI, Bradstock KF.

Br J Haematol. 1988 Jan;68(1):97-101.

PMID:
3345299
19.

Genetic abnormalities of Bernard-Soulier syndrome.

Kunishima S, Kamiya T, Saito H.

Int J Hematol. 2002 Nov;76(4):319-27. Review.

PMID:
12463594
20.

Bernard-Soulier syndrome: a case report.

Pansatiankul BJ, Opartkiattikul N, Sangtawesin W.

Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:219-21.

PMID:
7886580
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