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Transplantation Proceedings|December 20, 2007
Splenic artery steal syndrome in living donor liver transplantation: a case reportK Shimizu, H Tashiro, Y Fudaba, et al.
American Journal of Human Genetics|September 1, 1995
Mucopolysaccharidosis IVA: identification of a common missense mutation I113F in the N-Acetylgalactosamine-6-sulfate sulfatase geneS Tomatsu, S Fukuda, A Cooper, et al.
Pediatric Hematology and Oncology|October 23, 1998
Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocolY Yamada, R Inoue, T Fukao, et al.
No to Hattatsu = Brain and Development|March 1, 1996
[Early intervention for very-low-birth-weight infant]T Matsuishi, S Ishibashi, Y Yamashita, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1997
Eosinophil adhesion regulates RANTES production in nasal epithelial cellsN Terada, K Maesako, N Hamano, et al.
Japanese Journal of Clinical Oncology|March 25, 1999
A case of advanced esophageal cancer showing a long-term complete response with chemotherapy with nedaplatin aloneT Satoh, K Tsushima, S Saitoh, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 26, 2003
High frequency of antibiotic-associated diarrhea due to toxin A-negative, toxin B-positive Clostridium difficile in a hospital in Japan and risk factors for infectionM Komatsu, H Kato, M Aihara, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery|September 14, 2001
[Delayed traumatic diaphragmatic hernia diagnosed by magnetic resonance imaging and direct coronal computed tomography: report of a case]B Shirasawa, S Furukawa, T Tsushimi, et al.
Australasian Physical & Engineering Sciences in Medicine|November 9, 2018
AFOMP policy number 6: code of ethics for medical physicists in AFOMP CountriesW H Round, K H Ng, L Rodriguez, et al.
American Journal of Human Genetics|November 5, 1997
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorderY Suzuki, L L Jiang, M Souri, et al.
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