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Experimental and Therapeutic Medicine|November 16, 2022
Recombinant human soluble thrombomodulin and danaparoid combination anticoagulant therapy for disseminated intravascular coagulation in a child with streptococcal toxic shock syndrome: A case reportYutaka Kato, Hiroshi Kawaguchi, Shinichiro Iwataki, et al.Neurologia Medico-Chirurgica|June 25, 2011
Lateral buttock congenital dermal sinus tractSatoshi Yamaguchi, Masaaki Takeda, Hirotaka Kihara, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|January 19, 2023
Surfactant therapy using a bronchofiberscope in respiratory distress syndromeMasanori Wasa, Hisaya Hasegawa, Hirotaka Kihara, et al.Transfusion|August 24, 2017
Anti-human neutrophil antigen-1a, -1b, and -2 antibodies in neonates and children with immune neutropenias analyzed by extracted granulocyte antigen immunofluorescence assayRie Onodera, Emi Kurita, Kikuyo Taniguchi, et al.International Journal of Hematology|January 19, 2010
Significance of immature platelet fraction and CD41-positive cells at birth in early onset neonatal thrombocytopeniaHirotaka Kihara, Norioki Ohno, Syuhei Karakawa, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 24, 2020
Evaluation of respiratory center function in congenital central hypoventilation syndrome by monitoring electrical activity of the diaphragmYosuke Yamada, Hisaya Hasegawa, Nobuhide Henmi, et al.Journal of Pediatric Hematology/Oncology|July 9, 2003
Efficacy of prophylactic use of trimethoprim-sulfamethoxazole in autoimmune neutropenia in infancyMasao Kobayashi, Takashi Sato, Hiroshi Kawaguchi, et al.Blood|April 20, 2002
Significance of the detection of antineutrophil antibodies in children with chronic neutropeniaMasao Kobayashi, Kazuhiro Nakamura, Hiroshi Kawaguchi, et al.Pediatric Nephrology (Berlin, Germany)|April 17, 2002
A case of post-transplant hyperparathyroidism treated with ethanol injectionToshiyuki Ohta, Takashi Sakano, Shohei Fuchinoue, et al.American Journal of Human Genetics|May 28, 2019
Germline-Activating RRAS2 Mutations Cause Noonan SyndromeTetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.Pageof 1