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Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 1994
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV
K Zheng, P S Thorner, P Marrano, et al.
Neuropathology and Applied Neurobiology
|
November 7, 2007
Primary central nervous system plasmablastic lymphoma in AIDS
S Shuangshoti, T Assanasen, S Lerdlum, et al.
The International Journal of Pediatric Nephrology
|
June 1, 1984
Determination of circulating immune complexes, C3 and C4 complement components and anti-DNA antibody in different classes of lupus nephritis
M H Klein, P S Thorner, S J Yoon, et al.
Pathology
|
October 1, 1990
Xanthogranulomatous cholecystitis and cholecystoduodenal fistula formation associated with total parenteral nutrition in a six year old child
R W Byard, P S Thorner, E Cutz, et al.
Cancer
|
April 15, 1994
MYCN gene amplification in rhabdomyosarcoma
D Driman, P S Thorner, M L Greenberg, et al.
Seminars in Arthritis and Rheumatism
|
April 1, 1994
Localized scleroderma in childhood: a report of 30 cases
Y Uziel, B R Krafchik, E D Silverman, et al.
Pediatric Pathology
|
January 1, 1990
Pathological features of multiple endocrine neoplasia type IIb in childhood
R W Byard, P S Thorner, H S Chan, et al.
Cancer
|
November 15, 1992
Molecular genetic, cytogenetic, and immunohistochemical characterization of alveolar soft-part sarcoma. Implications for cell of origin
C Cullinane, P S Thorner, M L Greenberg, et al.
The American Journal of Pathology
|
June 11, 1999
Absence of the alpha6(IV) chain of collagen type IV in Alport syndrome is related to a failure at the protein assembly level and does not result in diffuse leiomyomatosis
K Zheng, S Harvey, Y Sado, et al.
The Journal of Pediatrics
|
May 1, 1982
Disseminated Legionella pneumophila infection in an infant with severe combined immunodeficiency
E Cutz, P S Thorner, C P Rao, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 1994
Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV
K Zheng, P S Thorner, P Marrano, et al.
Neuropathology and Applied Neurobiology
|
November 7, 2007
Primary central nervous system plasmablastic lymphoma in AIDS
S Shuangshoti, T Assanasen, S Lerdlum, et al.
The International Journal of Pediatric Nephrology
|
June 1, 1984
Determination of circulating immune complexes, C3 and C4 complement components and anti-DNA antibody in different classes of lupus nephritis
M H Klein, P S Thorner, S J Yoon, et al.
Pathology
|
October 1, 1990
Xanthogranulomatous cholecystitis and cholecystoduodenal fistula formation associated with total parenteral nutrition in a six year old child
R W Byard, P S Thorner, E Cutz, et al.
Cancer
|
April 15, 1994
MYCN gene amplification in rhabdomyosarcoma
D Driman, P S Thorner, M L Greenberg, et al.
Seminars in Arthritis and Rheumatism
|
April 1, 1994
Localized scleroderma in childhood: a report of 30 cases
Y Uziel, B R Krafchik, E D Silverman, et al.
Pediatric Pathology
|
January 1, 1990
Pathological features of multiple endocrine neoplasia type IIb in childhood
R W Byard, P S Thorner, H S Chan, et al.
Cancer
|
November 15, 1992
Molecular genetic, cytogenetic, and immunohistochemical characterization of alveolar soft-part sarcoma. Implications for cell of origin
C Cullinane, P S Thorner, M L Greenberg, et al.
The American Journal of Pathology
|
June 11, 1999
Absence of the alpha6(IV) chain of collagen type IV in Alport syndrome is related to a failure at the protein assembly level and does not result in diffuse leiomyomatosis
K Zheng, S Harvey, Y Sado, et al.
The Journal of Pediatrics
|
May 1, 1982
Disseminated Legionella pneumophila infection in an infant with severe combined immunodeficiency
E Cutz, P S Thorner, C P Rao, et al.
Page
of 8