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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1982 | 1 |
1984 | 1 |
2003 | 1 |
2004 | 1 |
2024 | 0 |
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Page 1
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome.
Blood. 2004 Feb 15;103(4):1305-10. doi: 10.1182/blood-2003-06-1796. Epub 2003 Oct 16.
Blood. 2004.
PMID: 14563640
Free article.
Congenital microangiopathic hemolytic anemia: report of a Japanese girl.
Shinohara T, Miyamura S, Suzuki E, Kobayashi K.
Shinohara T, et al.
Eur J Pediatr. 1982 Mar;138(2):191-3. doi: 10.1007/BF00441153.
Eur J Pediatr. 1982.
PMID: 7094941
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Efficacy of several plasma components in a young boy with chronic thrombocytopenia and hemolytic anemia who responds repeatedly to normal plasma infusions.
Miura M, Koizumi S, Nakamura K, Ohno T, Tachinami T, Yamagami M, Taniguchi N, Kinoshita S, Abildgaard CF.
Miura M, et al.
Am J Hematol. 1984 Oct;17(3):307-19. doi: 10.1002/ajh.2830170311.
Am J Hematol. 1984.
PMID: 6433703
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