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K Altland

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Der Internist|July 1, 1997
[Liver transplantation in familial amyloid polyneuropathy. Case report and review of the literature]M Krüger, K Altland, R P Linke, et al.
Progress in Clinical and Biological Research|January 1, 1982
Workshop on amniotic fluid AcetylcholinesteraseN Wald, R Harris, K Altland, et al.
The British Journal of Dermatology|November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German familyS Cichon, R Kruse, A M Hillmer, et al.
Basic Research in Cardiology|November 1, 1991
Transthyretin Leu 68 in a form of cardiac amyloidosisM R Almeida, A Hesse, A Steinmetz, et al.
American Journal of Human Genetics|May 1, 1991
Molecular analyses of an acidic transthyretin Asn 90 variantM J Saraiva, M R Almeida, I L Alves, et al.
Clinical Genetics|January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findingsA Ferlini, F Salvi, A Uncini, et al.
Lancet (London, England)|October 8, 1988
First-trimester biochemical screening for Down syndromeH S Cuckle, N J Wald, G Barkai, et al.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1993
Thyroxine binding in a TTR Met 119 kindredI L Alves, C M Divino, G C Schussler, et al.
Human Genetics|December 1, 1988
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian originM J Saraiva, P P Costa, M do R Almeida, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Der Internist|July 1, 1997
[Liver transplantation in familial amyloid polyneuropathy. Case report and review of the literature]M Krüger, K Altland, R P Linke, et al.
Progress in Clinical and Biological Research|January 1, 1982
Workshop on amniotic fluid AcetylcholinesteraseN Wald, R Harris, K Altland, et al.
The British Journal of Dermatology|November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German familyS Cichon, R Kruse, A M Hillmer, et al.
Basic Research in Cardiology|November 1, 1991
Transthyretin Leu 68 in a form of cardiac amyloidosisM R Almeida, A Hesse, A Steinmetz, et al.
American Journal of Human Genetics|May 1, 1991
Molecular analyses of an acidic transthyretin Asn 90 variantM J Saraiva, M R Almeida, I L Alves, et al.
Clinical Genetics|January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findingsA Ferlini, F Salvi, A Uncini, et al.
Lancet (London, England)|October 8, 1988
First-trimester biochemical screening for Down syndromeH S Cuckle, N J Wald, G Barkai, et al.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1993
Thyroxine binding in a TTR Met 119 kindredI L Alves, C M Divino, G C Schussler, et al.
Human Genetics|December 1, 1988
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian originM J Saraiva, P P Costa, M do R Almeida, et al.
Pageof 5