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Items: 1 to 20 of 81

1.

[Wiskott-Aldrich syndrome].

GELZER J, GASSER C.

Helv Paediatr Acta. 1961 Apr;16:17-39. German. No abstract available.

PMID:
13704318
2.

Platelet survival in Wiskott-Aldrich syndrome.

Pearson HA, Shulman NR, Oski FA, Eitzman DV.

J Pediatr. 1966 May;68(5):754-60. No abstract available.

PMID:
5948737
3.

Wiskott-Aldrich syndrome.

[No authors listed]

Arch Dermatol. 1969 Mar;99(3):372-3. No abstract available.

PMID:
5812955
4.

Eczema, thrombocytopenic purpura, and recurring infections; a familial disorder with report of four families.

MILLS SD, WINKELMANN RK.

AMA Arch Derm. 1959 Apr;79(4):466-72. No abstract available.

PMID:
13636432
5.

Wiskott-Aldrich syndrome (eczema, recurrent bleeding and recurrent upper respiratory infections).

MOYNAHAN EJ.

Proc R Soc Med. 1962 Mar;55:232-3. No abstract available.

6.

Eczema associated with thrombocytopenic purpura and purulent otitis media; report of five fatal cases.

HUNTLEY CC, DEES SC.

Pediatrics. 1957 Mar;19(3):351-61. No abstract available.

PMID:
13408013
7.

Aldrich's syndrome (thrombocytopenia, eczema, and infection infants); studies of the defense mechanisms.

KRIVIT W, GOOD RA.

AMA J Dis Child. 1959 Feb;97(2):137-53. No abstract available.

PMID:
13616861
8.

A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.

Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E.

Turk J Pediatr. 2006 Jan-Mar;48(1):66-8.

PMID:
16562789
9.

The development of malignancy in the course of the Aldrich syndrome.

ten Bensel RW, Stadlan EM, Krivit W.

J Pediatr. 1966 May;68(5):761-7. No abstract available.

PMID:
5948738
10.

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.

PMID:
15946311
11.

[THE ALDRICH SYNDROME (FAMILIAL THROMBOPENIC PURPURA, ECZEMA, RECURRING INFECTIONS)].

MARCHAL G, BILSKI-PASQUIER G, BONNET-GAJDOS M, SAMAMA M.

Presse Med. 1963 Dec 21;71:2621-4. French. No abstract available.

PMID:
14102410
12.
13.

Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.

Andreu N, Matamoros N, Escudero A, Fillat C.

Int J Mol Med. 2007 May;19(5):777-82.

PMID:
17390083
14.

Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation.

Jin Y, Mazza C, Christie JR, Giliani S, Fiorini M, Mella P, Gandellini F, Stewart DM, Zhu Q, Nelson DL, Notarangelo LD, Ochs HD.

Blood. 2004 Dec 15;104(13):4010-9. Epub 2004 Jul 29.

15.

[Fatal adrenal atrophy after prolonged corticotherapy in an infant].

PIERSON M, MANCIAUX M, REMIGY E, BARBELIN R.

Rev Med Nancy. 1960 Jul;85:616-9. French. No abstract available.

PMID:
14432876
16.

A child with multiple petechiae and eczematous plaques.

Moore MM, Hurst EB, Chastain S, Barnes CJ.

Pediatr Dermatol. 2007 Jul-Aug;24(4):417-8. No abstract available.

PMID:
17845172
17.

[THROMBOPENIA IN THE NEWBORN, WITH SPECIAL REFERENCE TO TRANSIENT NEONATAL THROMBOPENIA].

VAN DER WEERDT CM, VERSLUYS C.

Ned Tijdschr Geneeskd. 1964 Dec 26;108:2490-8. Dutch. No abstract available.

PMID:
14257816
18.

WISKOTT-ALDRICH'S SYNDROME: THROMBOCYTOPENIA, ECZEMA AND RECURRENT INFECTION.

HASTRUP J, GRAHL-MADSEN R.

Dan Med Bull. 1965 Aug;12:99-102. No abstract available.

PMID:
14342552
19.

Wiskott-Aldrich syndrome.

Notarangelo LD, Miao CH, Ochs HD.

Curr Opin Hematol. 2008 Jan;15(1):30-6. Review.

PMID:
18043243
20.

Symptom complexes, syndromes and eponyms.

[No authors listed]

N Engl J Med. 1967 Oct 26;277(17):933. No abstract available.

PMID:
6070345

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