Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 18

1.

Leukocyte adhesion deficiency mimicking Hirschsprung disease.

Rivera-Matos IR, Rakita RM, Mariscalco MM, Elder FF, Dreyer SA, Cleary TG.

J Pediatr. 1995 Nov;127(5):755-7. Review.

PMID:
7472832
2.

Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13.

Shanske A, Ferreira JC, Leonard JC, Fuller P, Marion RW.

Am J Med Genet. 2001 Aug 15;102(3):231-6. Review.

PMID:
11484199
3.

Leukocyte adhesion deficiency type 1: an important consideration in the clinical differential diagnosis of prepubertal periodontitis. A case report and review of the literature.

Cox DP, Weathers DR.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008 Jan;105(1):86-90. Epub 2007 Jul 6. Review.

PMID:
17618138
4.

[Hereditary polymorphonuclear neutrophil deficiencies].

Chollet-Martin S, Gougerot-Pocidalo MA.

Transfus Clin Biol. 2000 Dec;7(6):533-9. Review. French.

PMID:
11204838
5.

Gene therapy for leukocyte adhesion deficiency.

Bauer TR Jr, Hickstein DD.

Curr Opin Mol Ther. 2000 Aug;2(4):383-8. Review.

PMID:
11249768
6.

Leukocyte adhesion deficiency syndrome: report on the first case in Chile and South America.

Vásquez-De Kartzow R, Jesam C, Nehgme V, Várgas F, Sepúlveda C.

Sao Paulo Med J. 2012;130(4):263-6. Review.

7.

Retinoblastoma and Hirschsprung disease in a patient with interstitial deletion of chromosome 13.

Weigel BJ, Pierpont ME, Young TL, Mutchler SB, Neglia JP.

Am J Med Genet. 1998 May 26;77(4):285-8. Review.

PMID:
9600737
8.

Leukocyte CD11/CD18 integrins: biological and clinical relevance.

Mazzone A, Ricevuti G.

Haematologica. 1995 Mar-Apr;80(2):161-75. Review.

9.

Leukocyte adhesion deficiency syndromes: adhesion and tethering defects involving beta 2 integrins and selectin ligands.

Bunting M, Harris ES, McIntyre TM, Prescott SM, Zimmerman GA.

Curr Opin Hematol. 2002 Jan;9(1):30-5. Review.

PMID:
11753075
10.

Hematologically important mutations: leukocyte adhesion deficiency.

Roos D, Law SK.

Blood Cells Mol Dis. 2001 Nov-Dec;27(6):1000-4. Review.

PMID:
11831866
11.

Genetic analysis of integrin function in man: LAD-1 and other syndromes.

Hogg N, Bates PA.

Matrix Biol. 2000 Jul;19(3):211-22. Review.

PMID:
10936446
13.

Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?

Michaelis RC, Skinner SA, Deason R, Skinner C, Moore CL, Phelan MC.

Am J Med Genet. 1997 Aug 22;71(3):298-304. Review.

PMID:
9268100
14.

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

Fewtrell MS, Tam PK, Thomson AH, Fitchett M, Currie J, Huson SM, Mulligan LM.

J Med Genet. 1994 Apr;31(4):325-7. Review.

15.

Chemotaxis of non-compressed blood polymorphonuclear leukocytes from an adolescent with severe leukocyte adhesion deficiency.

Malawista SE, de Boisfleury Chevance A, Brown EJ, Boxer LA, Law SK.

Am J Hematol. 2003 Jun;73(2):115-20. Review.

16.

[Clinical aspects, genetics and immunology of leukocyte adhesion protein deficiencies].

Uhlig T, Belohradsky BH.

Ergeb Inn Med Kinderheilkd. 1993;61:1-55. Review. German. No abstract available.

PMID:
7900994
17.

Case 1: Recurrent Omphalitis and Nonhealing Ulcers in a 7-month-old Girl.

Sivathanu S, Sampath S, Sridhar I.

Pediatr Rev. 2016 Nov;37(11):491-493. Review. No abstract available.

PMID:
27803145
18.

[Hirshprung's disease, neuronal intestinal dysplasia, hypoganglionosis].

Kashimura H, Nakahara A, Fukutomi H.

Nihon Rinsho. 1994 Dec;Suppl 6:35-7. Review. Japanese. No abstract available.

PMID:
7837495

Supplemental Content

Support Center