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Ellen Fleischnick

TitleClinical Senior Instructor
InstitutionSchool of Medicine and Dentistry
AddressPark Ridge Behav Health
1565 Long Pond Road
Rochester NY 14626
 Selected Publications
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  1. Hauser SL, Fleischnick E, Weiner HL, Marcus D, Awdeh Z, Yunis EJ, Alper CA. Extended major histocompatibility complex haplotypes in patients with multiple sclerosis. Neurology. 1989 Feb; 39(2 Pt 1):275-7.
    View in: PubMed
  2. Whitehead AS, Truedsson L, Schneider PM, Awdeh ZL, Fleischnick E, Blumenthal M, Costello W, Gerald PS, Yunis EJ, Alper CA. The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes. Hum Immunol. 1988 Jan; 21(1):23-32.
    View in: PubMed
  3. Boustany RM, Fleischnick E, Alper CA, Marazita ML, Spence MA, Martin JB, Kolodny EH. The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree. Neurology. 1987 Jun; 37(6):910-5.
    View in: PubMed
  4. Alper CA, Fleischnick E, Awdeh Z, Katz AJ, Yunis EJ. Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy. J Clin Invest. 1987 Jan; 79(1):251-6.
    View in: PubMed
  5. Liberfarb RM, Katsumi O, Fleischnick E, Shapiro F, Hirose T. Tapetoretinal degeneration associated with multisystem abnormalities. A case report. Ophthalmic Paediatr Genet. 1986 Dec; 7(3):151-8.
    View in: PubMed
  6. Eisenbarth GS, Srikanta S, Fleischnick E, Ganda OP, Jackson RA, Brink SJ, Soeldner JS, Yunis EJ, Alper C. Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4. Diabetes Care. 1985 Sep-Oct; 8(5):477-80.
    View in: PubMed
  7. Yunis EJ, Awdeh Z, Johnson A, Suciu-Foca N, Robinson MA, Hartzman R, Raum D, Fleischnick E, Alper CA. Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B. Immunogenetics. 1985; 21(1):25-31.
    View in: PubMed
  8. Alper CA, Fleischnick E, Awdeh Z, Raum D, Crigler JF, Gerald PS, Yunis EJ. Extended MHC haplotypes in salt-losing 21-hydroxylase deficiency. Ann N Y Acad Sci. 1985; 458:28-35.
    View in: PubMed
  9. Srikanta S, Ganda OP, Jackson RA, Brink SJ, Fleischnick E, Yunis E, Alper C, Soeldner JS, Eisenbarth GS. Pre-type 1 (insulin-dependent) diabetes: common endocrinological course despite immunological and immunogenetic heterogeneity. Diabetologia. 1984 Jul; 27 Suppl:146-8.
    View in: PubMed
  10. Whitehead AS, Woods DE, Fleischnick E, Chin JE, Yunis EJ, Katz AJ, Gerald PS, Alper CA, Colten HR. DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex. N Engl J Med. 1984 Jan 12; 310(2):88-91.
    View in: PubMed
  11. Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents. Pediatrics. 1983 Nov; 72(5):690-5.
    View in: PubMed
  12. Fleischnick E, Awdeh ZL, Raum D, Granados J, Alosco SM, Crigler JF, Gerald PS, Giles CM, Yunis EJ, Alper CA. Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients. Lancet. 1983 Jan 22; 1(8317):152-6.
    View in: PubMed


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