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Pediatric Research|October 22, 2004
Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosisToshiyuki Fukao, Haruo Shintaku, Ryou Kusubae, et al.
American Journal of Clinical Pathology|April 1, 1984
Keratins of different molecular weight in exfoliated mesothelial and adenocarcinoma cells--an aid to cell identificationA E Walts, J W Said, I P Shintaku, et al.
Archives of Pathology & Laboratory Medicine|July 1, 1997
Donor origin of posttransplant lymphoproliferative disorder localized to a liver allograft: demonstration by fluorescence in situ hybridizationM A Lones, D Lopez-Terrada, L M Weiss, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 2, 2009
Comparison of fluorescent in situ hybridization HER-2/neu results on core needle biopsy and excisional biopsy in primary breast cancerSophia K Apple, Alarice C Lowe, P Nagesh Rao, et al.
European Journal of Pediatrics|August 1, 1986
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuriaA Niederwieser, H Shintaku, T Hasler, et al.
The American Journal of Pathology|February 1, 1991
Absence of bcl-2 major breakpoint region and JH gene rearrangement in lymphocyte predominance Hodgkin's disease. Results of Southern blot analysis and polymerase chain reactionJ W Said, A F Sassoon, I P Shintaku, et al.
The American Journal of Dermatopathology|June 21, 2013
Malignant melanoma with neural differentiation: an exceptional case report and brief review of the pertinent literatureAlbert Su, Sarah M Dry, Scott W Binder, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|October 15, 2013
Melorheostosis and central giant cell granuloma of the mandible in a 15-year-old girlK M Anderson, W H Shintaku, M S Rosebush, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|November 29, 2020
Guidelines for oral and maxillofacial imaging: COVID-19 considerationsDavid S MacDonald, Dan C Colosi, Muralidhar Mupparapu, et al.
European Journal of Pediatrics|May 1, 1987
"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosityA Niederwieser, H Shintaku, W Leimbacher, et al.
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