Makoto Takagi, MD

Neurology Tokyo Saiseikai Hospital, Minato-ku, Tōkyō-to, Japan 
"Makoto Takagi"

Mean distance: 19.07 (cluster 24)
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Ono T, Isobe T, Morita Y, et al. (2016) Effects of parity and season on pregnancy rates after the transfer of embryos to repeat-breeder Japanese Black beef cattle Archiv Tierzucht. 59: 45-49
Yagi H, Takagi M, Narumi S, et al. (2016) Stippled calcification in an infant with a recurrent SRCAP gene mutation American Journal of Medical Genetics, Part A
Nakata K, Komukai K, Yoshii Y, et al. (2015) The Optimal Cut-off Value of Plasma BNP to Differentiate Heart Failure in the Emergency Department in Japanese Patients with Dyspnea. Internal Medicine (Tokyo, Japan). 54: 2975-80
Takagi M, Shimizu M, Suzuki E, et al. (2015) Whole exome sequencing identified a novel COL2A1 mutation that causes mild Spondylo-epiphyseal dysplasia mimicking autosomal dominant brachyolmia. American Journal of Medical Genetics. Part A
Ishizaka M, Gohda T, Takagi M, et al. (2015) Podocyte-specific deletion of Rac1 leads to aggravation of renal injury in STZ-induced diabetic mice. Biochemical and Biophysical Research Communications. 467: 549-55
Yamakawa H, Yoshida M, Yamada M, et al. (2015) Pulmonary tumor thrombotic microangiopathy associated with urothelial carcinoma of the urinary bladder: antemortem diagnosis by pulmonary microvascular cytology. Clinical Case Reports. 3: 735-9
Yamakawa H, Shimizu K, Michimoto K, et al. (2015) Transcatheter embolization for hemoptysis associated with anomalous systemic artery in a patient with scimitar syndrome. Springerplus. 4: 422
Sugioka K, Takagi M, Sakamoto S, et al. (2015) Predictors of silent brain infarction on magnetic resonance imaging in patients with nonvalvular atrial fibrillation: A transesophageal echocardiographic study. American Heart Journal. 169: 783-90
Sakamoto S, Takagi M, Tatsumi H, et al. (2015) Utility of T-wave alternans during night time as a predictor for ventricular fibrillation in patients with Brugada syndrome. Heart and Vessels
Takagi M, Shinohara H, Narumi S, et al. (2015) Severe osteogenesis imperfecta caused by double glycine substitutions near the amino-terminal triple helical region in COL1A2. American Journal of Medical Genetics. Part A. 167: 1627-31
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