Search Results - "FLEISCHNICK, E"

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  1. 1

    Extended major histocompatibility complex haplotypes in patients with multiple sclerosis by HAUSER, S. L, FLEISCHNICK, E, WEINER, H. L, MARCUS, D, AWDEH, Z, YUNIS, E. J, ALPER, C. A

    Published in Neurology (01-02-1989)
    “…We derived complete haplotypes of the major histocompatibility complex for 33 patients with MS and their families. The DR2 allele and DR2-bearing extended…”
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  2. 2

    Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy by ALPER, C. A, FLEISCHNICK, E, ZUHEIR AWDEH, KATZ, A. J, YUNIS, E. J

    “…We have studied major histocompatibility complex markers in randomly ascertained Caucasian patients with gluten-sensitive enteropathy and their families. The…”
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  3. 3

    Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents by EMANS, S. J, GRACE, E, FLEISCHNICK, E, MANSFIELD, M. J, CRIGLER, J. F. JR

    Published in Pediatrics (Evanston) (01-11-1983)
    “…Because severe hirsutism is difficult to reverse, the evaluation of the adolescent girl with progressive hirsutism should aim at the pathophysiology of…”
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  4. 4

    The autosomal dominant form of pure familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree by BOUSTANY, R-M. N, FLEISCHNICK, E, ALPER, C. A, MARAZITA, M. L, SPENCE, M. A, MARTIN, J. B, KOLODNY, E. H

    Published in Neurology (01-06-1987)
    “…We studied 33 affected members in a family with autosomal dominant "pure" familial spastic paraplegia (FSP). Symptoms began in the fourth or fifth decade,…”
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  5. 5

    Pre-type 1 (insulin-dependent) diabetes: common endocrinological course despite immunological and immunogenetic heterogeneity by Srikanta, S, Ganda, O P, Jackson, R A, Brink, S J, Fleischnick, E, Yunis, E, Alper, C, Soeldner, J S, Eisenbarth, G S

    Published in Diabetologia (01-07-1984)
    “…In an ongoing prospective study 32 individuals have been evaluated for insulin secretory dynamics, islet cell antibodies and HLA antigens, during the…”
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  6. 6

    Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4 by Eisenbarth, G S, Srikanta, S, Fleischnick, E, Ganda, O P, Jackson, R A, Brink, S J, Soeldner, J S, Yunis, E J, Alper, C

    Published in Diabetes care (01-09-1985)
    “…Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4. G S Eisenbarth , S Srikanta , E Fleischnick , O P…”
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  7. 7

    The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes by Whitehead, A S, Truedsson, L, Schneider, P M, Awdeh, Z L, Fleischnick, E, Blumenthal, M, Costello, W, Gerald, P S, Yunis, E J, Alper, C A

    Published in Human immunology (01-01-1988)
    “…A C4 DNA polymorphism that can subdivide C4 allotypes and major histocompatibility complex-linked complement gene cluster allele combinations (complotypes)…”
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  8. 8

    Tapetoretinal degeneration associated with multisystem abnormalities. A case report by Liberfarb, R M, Katsumi, O, Fleischnick, E, Shapiro, F, Hirose, T

    “…Tapetoretinal degeneration is not infrequently associated with other systemic abnormalities. The authors have examined an 11-year-old girl with severe…”
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  9. 9

    DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex by Whitehead, A S, Woods, D E, Fleischnick, E, Chin, J E, Yunis, E J, Katz, A J, Gerald, P S, Alper, C A, Colten, H R

    Published in The New England journal of medicine (12-01-1984)
    “…Polymorphisms of the proteins encoded by genes that lie within the major histocompatibility complex (MHC) have served as useful markers for organ…”
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  10. 10

    Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients by Fleischnick, E, Awdeh, Z L, Raum, D, Granados, J, Alosco, S M, Crigler, Jr, J F, Gerald, P S, Giles, C M, Yunis, E J, Alper, C A

    Published in The Lancet (British edition) (22-01-1983)
    “…HLA, complement, and glyoxalase I alleles were studied in 29 families in which at least one member has classical 21-hydroxylase-deficiency congenital adrenal…”
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    Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B by YUNIS, E. J, AWDEH, Z, JOHNSON, A, SUCIU-FOCA, N, ROBINSON, M. A, HARTZMAN, R, RAUM, D, FLEISCHNICK, E, ALPER, C. A

    Published in Immunogenetics (New York) (1985)
    “…The loci for BF, C2, C4A, and C4B are very closely linked to each other so that alleles of these plasma protein markers occur in populations in linkage…”
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