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E Fleischnick

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Ophthalmic Paediatrics and Genetics|December 1, 1986
Tapetoretinal degeneration associated with multisystem abnormalities. A case reportR M Liberfarb, O Katsumi, E Fleischnick, et al.
The Journal of Clinical Investigation|January 1, 1987
Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathyC A Alper, E Fleischnick, Z Awdeh, et al.
Pediatrics|November 1, 1983
Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescentsS J Emans, E Grace, E Fleischnick, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Extended MHC haplotypes in salt-losing 21-hydroxylase deficiencyC A Alper, E Fleischnick, Z Awdeh, et al.
Neurology|February 1, 1989
Extended major histocompatibility complex haplotypes in patients with multiple sclerosisS L Hauser, E Fleischnick, H L Weiner, et al.
Neurology|June 1, 1987
The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigreeR M Boustany, E Fleischnick, C A Alper, et al.
Immunogenetics|January 1, 1985
Complotype genetic loci segregate more frequently with HLA-DR than with HLA-BE J Yunis, Z Awdeh, A Johnson, et al.
Diabetologia|July 1, 1984
Pre-type 1 (insulin-dependent) diabetes: common endocrinological course despite immunological and immunogenetic heterogeneityS Srikanta, O P Ganda, R A Jackson, et al.
Human Immunology|January 1, 1988
The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypesA S Whitehead, L Truedsson, P M Schneider, et al.
Diabetes Care|September 1, 1985
Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4G S Eisenbarth, S Srikanta, E Fleischnick, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Ophthalmic Paediatrics and Genetics|December 1, 1986
Tapetoretinal degeneration associated with multisystem abnormalities. A case reportR M Liberfarb, O Katsumi, E Fleischnick, et al.
The Journal of Clinical Investigation|January 1, 1987
Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathyC A Alper, E Fleischnick, Z Awdeh, et al.
Pediatrics|November 1, 1983
Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescentsS J Emans, E Grace, E Fleischnick, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Extended MHC haplotypes in salt-losing 21-hydroxylase deficiencyC A Alper, E Fleischnick, Z Awdeh, et al.
Neurology|February 1, 1989
Extended major histocompatibility complex haplotypes in patients with multiple sclerosisS L Hauser, E Fleischnick, H L Weiner, et al.
Neurology|June 1, 1987
The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigreeR M Boustany, E Fleischnick, C A Alper, et al.
Immunogenetics|January 1, 1985
Complotype genetic loci segregate more frequently with HLA-DR than with HLA-BE J Yunis, Z Awdeh, A Johnson, et al.
Diabetologia|July 1, 1984
Pre-type 1 (insulin-dependent) diabetes: common endocrinological course despite immunological and immunogenetic heterogeneityS Srikanta, O P Ganda, R A Jackson, et al.
Human Immunology|January 1, 1988
The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypesA S Whitehead, L Truedsson, P M Schneider, et al.
Diabetes Care|September 1, 1985
Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4G S Eisenbarth, S Srikanta, E Fleischnick, et al.
Pageof 2