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Results: 1 to 20 of 102

Similar articles for PubMed (Select 8871944)

1.

Immunogenetic studies in autism and related disorders.

Warren RP, Singh VK, Averett RE, Odell JD, Maciulis A, Burger RA, Daniels WW, Warren WL.

Mol Chem Neuropathol. 1996 May-Aug;28(1-3):77-81. Review.

PMID:
8871944
2.

Increased frequency of the null allele at the complement C4b locus in autism.

Warren RP, Singh VK, Cole P, Odell JD, Pingree CB, Warren WL, White E.

Clin Exp Immunol. 1991 Mar;83(3):438-40.

3.

Confirmation of the association of the C4B null allelle in autism.

Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, Stubbs G, Henley K, Torres A.

Hum Immunol. 2005 Feb;66(2):140-5.

PMID:
15694999
4.

C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism.

Sweeten TL, Odell DW, Odell JD, Torres AR.

BMC Med Genet. 2008 Jan 7;9:1. doi: 10.1186/1471-2350-9-1.

5.

Association of genes within the major histocompatibility complex with attention deficit hyperactivity disorder.

Odell JD, Warren RP, Warren WL, Burger RA, Maciulis A.

Neuropsychobiology. 1997;35(4):181-6.

PMID:
9246218
6.

Strong association of the third hypervariable region of HLA-DR beta 1 with autism.

Warren RP, Odell JD, Warren WL, Burger RA, Maciulis A, Daniels WW, Torres AR.

J Neuroimmunol. 1996 Jul;67(2):97-102.

PMID:
8765331
7.

Reading disability, attention-deficit hyperactivity disorder, and the immune system.

Warren RP, Odell JD, Warren WL, Burger RA, Maciulis A, Daniels WW, Torres AR.

Science. 1995 May 12;268(5212):786-8. No abstract available.

PMID:
7605493
8.

The link of C4B null allele to autism and to a family history of autoimmunity in Egyptian autistic children.

Mostafa GA, Shehab AA.

J Neuroimmunol. 2010 Jun;223(1-2):115-9. doi: 10.1016/j.jneuroim.2010.03.025. Epub 2010 May 10.

PMID:
20452682
9.

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.

Warren RP, Singh VK, Cole P, Odell JD, Pingree CB, Warren WL, DeWitt CW, McCullough M.

Immunogenetics. 1992;36(4):203-7.

PMID:
1639438
10.

Decreased plasma concentrations of the C4B complement protein in autism.

Warren RP, Burger RA, Odell D, Torres AR, Warren WL.

Arch Pediatr Adolesc Med. 1994 Feb;148(2):180-3.

PMID:
8118537
11.

Complete deficiencies of complement C4A and C4B including 2-bp insertion in codon 1213 are genetic risk factors of systemic lupus erythematosus in Thai populations.

Ittiprasert W, Kantachuvesiri S, Pavasuthipaisit K, Verasertniyom O, Chaomthum L, Totemchokchyakarn K, Kitiyanant Y.

J Autoimmun. 2005 Aug;25(1):77-84.

PMID:
15998580
12.
13.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
14.

Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.

Blanchong CA, Chung EK, Rupert KL, Yang Y, Yang Z, Zhou B, Moulds JM, Yu CY.

Int Immunopharmacol. 2001 Mar;1(3):365-92. Review.

PMID:
11367523
15.

Investigation on the possible relationship existing between the HLA-DR gene and attention deficit hyperactivity disorder and/or mental retardation.

Aureli A, Sebastiani P, Del Beato T, Marimpietri A, Melillo V, Sechi E, Di Loreto S.

Int J Immunopathol Pharmacol. 2008 Oct-Dec;21(4):985-91.

PMID:
19144284
16.

DR-positive T cells in autism: association with decreased plasma levels of the complement C4B protein.

Warren RP, Yonk J, Burger RW, Odell D, Warren WL.

Neuropsychobiology. 1995;31(2):53-7.

PMID:
7760985
17.

Brief report: immunoglobulin A deficiency in a subset of autistic subjects.

Warren RP, Odell JD, Warren WL, Burger RA, Maciulis A, Daniels WW, Torres AR.

J Autism Dev Disord. 1997 Apr;27(2):187-92. No abstract available.

PMID:
9105969
18.

The association and linkage of the HLA-A2 class I allele with autism.

Torres AR, Sweeten TL, Cutler A, Bedke BJ, Fillmore M, Stubbs EG, Odell D.

Hum Immunol. 2006 Apr-May;67(4-5):346-51. Epub 2006 Apr 3.

PMID:
16720216
19.

Complement C4B null allele status confers risk for systemic lupus erythematosus in a Spanish population.

Naves M, Hajeer AH, Teh LS, Davies EJ, Ordi-Ros J, Perez-Pemen P, Vilardel-Tarres M, Thomson W, Worthington J, Ollier WE.

Eur J Immunogenet. 1998 Aug;25(4):317-20.

PMID:
9777334
20.

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.

Smalley SL, Kustanovich V, Minassian SL, Stone JL, Ogdie MN, McGough JJ, McCracken JT, MacPhie IL, Francks C, Fisher SE, Cantor RM, Monaco AP, Nelson SF.

Am J Hum Genet. 2002 Oct;71(4):959-63. Epub 2002 Aug 14.

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