Makoto Takagi, MD
Affiliations: | Neurology | Tokyo Saiseikai Hospital, Minato-ku, Tōkyō-to, Japan |
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"Makoto Takagi"Bio:
http://stroke.ahajournals.org/cgi/reprint/20/5/680.pdf
Mean distance: 19.07 (cluster 24) | S | N | B | C | P |
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Publications
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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 |