Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms

Por Shovlin, C., Letarte, M.
Publicado em 1999

Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease

Por Abdalla, S A, Letarte, M
Publicado em 2006

Assessment of antigen-specific receptor function of surface immunoglobulin M and D with identical hapten specificity.

Por Tisch, R, Watanabe, M, Letarte, M, Hozumi, N
Publicado em 1987

No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia

Por Karabegovic, A, Shinawi, M, Cymerman, U, Letarte, M
Publicado em 2004

Purification and characterization of the P-80 glycoprotein from human brain.

Por Girgrah, N, Cruz, T F, Letarte, M, Moscarello, M A
Publicado em 1988

Identification of three antigens in human brain associated with similar antigens on human leukaemic cells.

Por Quackenbush, E J, Cruz, T F, Moscarello, M A, Letarte, M
Publicado em 1985

Identification of a polymorphism in human CD44

Por Dadi, H.K., Greaves, A.M., Cox, D.W., Letarte, M.
Publicado em 1991

Purification and characterization of a protein antigen (p94) from human brain and its identification in other species.

Por Cruz, T F, Girgrah, N, Quackenbush, E J, Letarte, M, Moscarello, M A
Publicado em 1987

Organization and Expression Strategy of the Ambisense Genome of Densonucleosis Virus of Galleria mellonella

Por Tijssen, P., Li, Y., El-Far, M., Szelei, J., Letarte, M., Zádori, Z.
Publicado em 2003

Common acute lymphoblastic leukemia antigen expressed on leukemia and melanoma cell lines has neutral endopeptidase activity.

Por Jongeneel, C V, Quackenbush, E J, Ronco, P, Verroust, P, Carrel, S, Letarte, M
Publicado em 1989

Mutant endoglin in hereditary hemorrhagic telangiectasia type 1 is transiently expressed intracellularly and is not a dominant negative.

Por Pece, N, Vera, S, Cymerman, U, White, R I, Wrana, J L, Letarte, M
Publicado em 1997

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2

Por Abdalla, S, Geisthoff, U, Bonneau, D, Plauchu, H, McDonald, J, Kennedy, S, Faughnan, M, Letarte, M
Publicado em 2003

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations

Por Prigoda, N L, Savas, S, Abdalla, S A, Piovesan, B, Rushlow, D, Vandezande, K, Zhang, E, Ozcelik, H, Gallie, B L, Letarte, M
Publicado em 2006