144 related articles for article (PubMed ID: 4168739)
21. [Congenital thrombocytopenia in adults].
van Zweeden A; Bot P; Smets Y; Terpstra W
Ned Tijdschr Geneeskd; 2011; 155():A2634. PubMed ID: 21382213
[TBL] [Abstract][Full Text] [Related]
22. [Mutation of WASP in Wiskott-Aldrich syndrome and it's effect on megakaryopoiesis].
Nonoyama S
Rinsho Ketsueki; 1998 Feb; 39(2):133-4. PubMed ID: 9545824
[No Abstract] [Full Text] [Related]
23. [Immunological aspects of Aldrich syndrome].
Iacovacci G; Ungari S; Aiuti F
Minerva Dermatol; 1967 Aug; 42(8):421. PubMed ID: 4178812
[No Abstract] [Full Text] [Related]
24. Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity.
Cooper MD; Chae HP; Lowman JT; Krivit W; Good RA
Am J Med; 1968 Apr; 44(4):499-513. PubMed ID: 4171085
[No Abstract] [Full Text] [Related]
25. [Congenital thrombopathies].
Outeiriño Hernanz J; Sánchez Fayos J
Rev Clin Esp; 1973 Jan; 128(2):93-100. PubMed ID: 4571943
[No Abstract] [Full Text] [Related]
26. [Post-transfusion autoimmune thrombocytopenia purpura syndrome].
Walewska I
Acta Haematol Pol; 1971; 2(3):259-64. PubMed ID: 4949897
[No Abstract] [Full Text] [Related]
27. [THROMBOPENIA IN THE NEWBORN, WITH SPECIAL REFERENCE TO TRANSIENT NEONATAL THROMBOPENIA].
VAN DER WEERDT CM; VERSLUYS C
Ned Tijdschr Geneeskd; 1964 Dec; 108():2490-8. PubMed ID: 14257816
[No Abstract] [Full Text] [Related]
28. Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome.
Donnér M; Schwartz M; Carlsson KU; Holmberg L
Blood; 1988 Dec; 72(6):1849-53. PubMed ID: 2904289
[TBL] [Abstract][Full Text] [Related]
29. Thrombocytokinetic examination in patients with hereditary thrombocytopenia.
Fortýnová J; Farská I; Pudlák P; Krecek M; Májský A; Vopatová M
Acta Univ Carol Med Monogr; 1972; 53():345-51. PubMed ID: 4677607
[No Abstract] [Full Text] [Related]
30. [Persistent thrombocytopenia in a child: morphological examination of blood platelets established the diagnosis of Wiskott-Aldrich syndrome].
Latger-Cannard V; Lacroix F; Devignes J; Salignac S; Bensoussan D; Salmon A; Mansuy L; Bordigoni P; Lecompte T
Ann Biol Clin (Paris); 2008; 66(1):100-4. PubMed ID: 18227012
[TBL] [Abstract][Full Text] [Related]
31. X-linked thrombocytopenic purpura. I. Clinical and genetic studies of a kindred.
Chiaro JJ; Dharmkrong-at A; Bloom GE
Am J Dis Child; 1972 Jun; 123(6):565-8. PubMed ID: 4624439
[No Abstract] [Full Text] [Related]
32. Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Crestani E; Volpi S; Candotti F; Giliani S; Notarangelo LD; Chu J; Aldave Becerra JC; Buchbinder D; Chou J; Geha RS; Kanariou M; King A; Mazza C; Moratto D; Sokolic R; Garabedian E; Porta F; Putti MC; Wakim RH; Tsitsikov E; Pai SY; Notarangelo LD
J Allergy Clin Immunol; 2015 Nov; 136(5):1401-4.e1-3. PubMed ID: 26409660
[TBL] [Abstract][Full Text] [Related]
33. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.
De Saint-Basile G; Schlegel N; Caniglia M; Le Deist F; Kaplan C; Lecompte T; Piller F; Fischer A; Griscelli C
Ann Hematol; 1991 Aug; 63(2):107-10. PubMed ID: 1912030
[TBL] [Abstract][Full Text] [Related]
34. Hematopoietic stem cell transplantation for X-linked thrombocytopenia from a mild symptomatic carrier.
Okuya M; Kurosawa H; Kubota T; Endoh K; Ogiwara A; Nonoyama S; Hagisawa S; Sato Y; Matsushita T; Fukushima K; Sugita K; Sato T; Arisaka O
Bone Marrow Transplant; 2010 Mar; 45(3):607-9. PubMed ID: 19684625
[No Abstract] [Full Text] [Related]
35. Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
Proust A; Guillet B; Pellier I; Rachieru P; Hoarau C; Claeyssens S; Léonard C; Charrier S; Vainchenker W; Tchernia G; Delaunay J
Eur J Haematol; 2005 Jul; 75(1):54-9. PubMed ID: 15946311
[TBL] [Abstract][Full Text] [Related]
36. [Chronic familial thrombopenia. Considerations on a clinical case].
Rusnac C; Horga L; Nussbaum V; Adler M; Ajtai A
Rev Pediatr Obstet Ginecol Pediatr; 1982; 31(4):371-5. PubMed ID: 6820564
[No Abstract] [Full Text] [Related]
37. Hereditary thrombocytopenia with an intrinsic platelet defect.
Murphy S; Oski FA; Gardner FH
N Engl J Med; 1969 Oct; 281(16):857-62. PubMed ID: 5818100
[No Abstract] [Full Text] [Related]
38. [Wiskott-Aldrich syndrome in a hetrozygous woman].
Tornai I; Kiss A; Laczkó J; Nagy PM
Orv Hetil; 1989 Mar; 130(13):679-82. PubMed ID: 2657554
[TBL] [Abstract][Full Text] [Related]
39. [Wiscott-Aldrich syndrome. Description of a case].
Brai M; Balsamo V; Mogavero S; Romano N; Lagrutta A
G Batteriol Virol Immunol; 1975; 68(1-6):130-9. PubMed ID: 1081964
[TBL] [Abstract][Full Text] [Related]
40. The bleeding time as a screening test for evaluation of platelet function.
Harker LA; Slichter SJ
N Engl J Med; 1972 Jul; 287(4):155-9. PubMed ID: 4537519
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]