| Year |
Citation |
Score |
| 2016 |
Ono T, Isobe T, Morita Y, Do LTK, Tanihara F, Taniguchi M, Takagi M, Otoi T. 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. DOI: 10.5194/aab-59-45-2016 |
0.308 |
|
| 2016 |
Yagi H, Takagi M, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y. Stippled calcification in an infant with a recurrent SRCAP gene mutation American Journal of Medical Genetics, Part A. DOI: 10.1002/ajmg.a.37516 |
0.427 |
|
| 2015 |
Nakata K, Komukai K, Yoshii Y, Miyanaga S, Kubota T, Kosuga T, Suzuki K, Yamada T, Yoshida J, Kimura H, Takagi M, Shimizu M, Yoshimura M. 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. PMID 26631879 DOI: 10.2169/internalmedicine.54.4786 |
0.447 |
|
| 2015 |
Takagi M, Shimizu M, Suzuki E, Shinohara H, Narumi S, Hasegawa T, Nishimura G, Hasegawa Y. 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. PMID 26586363 DOI: 10.1002/ajmg.a.37481 |
0.447 |
|
| 2015 |
Ishizaka M, Gohda T, Takagi M, Omote K, Sonoda Y, Oliva Trejo JA, Asao R, Hidaka T, Asanuma K, Horikoshi S, Tomino Y. Podocyte-specific deletion of Rac1 leads to aggravation of renal injury in STZ-induced diabetic mice. Biochemical and Biophysical Research Communications. 467: 549-55. PMID 26435502 DOI: 10.1016/j.bbrc.2015.09.158 |
0.351 |
|
| 2015 |
Yamakawa H, Yoshida M, Yamada M, Ishikawa T, Takagi M, Katagi H, Yoshida J, Kosuga T, Kuwano K. Pulmonary tumor thrombotic microangiopathy associated with urothelial carcinoma of the urinary bladder: antemortem diagnosis by pulmonary microvascular cytology. Clinical Case Reports. 3: 735-9. PMID 26401277 DOI: 10.1002/ccr3.330 |
0.318 |
|
| 2015 |
Yamakawa H, Shimizu K, Michimoto K, Kameoka Y, Kang R, Yoshida J, Yamada M, Yoshida M, Ishikawa T, Takagi M, Kuwano K. Transcatheter embolization for hemoptysis associated with anomalous systemic artery in a patient with scimitar syndrome. Springerplus. 4: 422. PMID 26301169 DOI: 10.1186/s40064-015-1219-9 |
0.333 |
|
| 2015 |
Sugioka K, Takagi M, Sakamoto S, Fujita S, Ito A, Iwata S, Matsumura Y, Nakagawa M, Doi A, Miki Y, Yoshiyama M, Ueda M. 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. PMID 26027615 DOI: 10.1016/j.ahj.2015.03.016 |
0.349 |
|
| 2015 |
Sakamoto S, Takagi M, Tatsumi H, Doi A, Sugioka K, Hanatani A, Yoshiyama M. Utility of T-wave alternans during night time as a predictor for ventricular fibrillation in patients with Brugada syndrome. Heart and Vessels. PMID 25989739 DOI: 10.1007/s00380-015-0692-y |
0.351 |
|
| 2015 |
Takagi M, Shinohara H, Narumi S, Nishimura G, Hasegawa Y, Hasegawa T. 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. PMID 25858481 DOI: 10.1002/ajmg.a.37051 |
0.468 |
|
| 2015 |
Nakamura Y, Takagi M, Yoshihashi H, Miura M, Narumi S, Hasegawa T, Miyake Y, Hasegawa Y. A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of Sotos syndrome. American Journal of Medical Genetics. Part A. 167: 1171-4. PMID 25712828 DOI: 10.1002/ajmg.a.36996 |
0.462 |
|
| 2015 |
Miki H, Takagi M. Design of serum-free medium for suspension culture of CHO cells on the basis of general commercial media. Cytotechnology. 67: 689-97. PMID 25149286 DOI: 10.1007/s10616-014-9778-0 |
0.348 |
|
| 2015 |
Yamakawa H, Shimizu K, Michimoto K, Kameoka Y, Kang R, Yoshida J, Yamada M, Yoshida M, Ishikawa T, Takagi M, Kuwano K. Transcatheter embolization for hemoptysis associated with anomalous systemic artery in a patient with scimitar syndrome Springerplus. 4. DOI: 10.1186/s40064-015-1219-9 |
0.303 |
|
| 2014 |
Tanaka E, Asanuma K, Kim E, Sasaki Y, Oliva Trejo JA, Seki T, Nonaka K, Asao R, Nagai-Hosoe Y, Akiba-Takagi M, Hidaka T, Takagi M, Koyanagi A, Mizutani S, Yagita H, et al. Notch2 activation ameliorates nephrosis. Nature Communications. 5: 3296. PMID 24526233 DOI: 10.1038/ncomms4296 |
0.357 |
|
| 2014 |
Takagi M, Narumi S, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T. A novel mutation in SOX2 causes hypogonadotropic hypogonadism with mild ocular malformation. Hormone Research in Pã¦Diatrics. 81: 133-8. PMID 24457197 DOI: 10.1159/000355279 |
0.457 |
|
| 2014 |
Kitaoka T, Miyoshi Y, Namba N, Miura K, Kubota T, Ohata Y, Fujiwara M, Takagi M, Hasegawa T, Jüppner H, Ozono K. Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature. European Journal of Pediatrics. 173: 799-804. PMID 24390061 DOI: 10.1007/s00431-013-2252-8 |
0.402 |
|
| 2013 |
Kodama F, Asanuma K, Takagi M, Hidaka T, Asanuma E, Fukuda H, Seki T, Takeda Y, Hosoe-Nagai Y, Asao R, Horikoshi S, Tomino Y. Translocation of dendrin to the podocyte nucleus in acute glomerular injury in patients with IgA nephropathy. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 28: 1762-72. PMID 23143340 DOI: 10.1093/ndt/gfs500 |
0.385 |
|
| 2012 |
Takagi M, Ishii T, Inokuchi M, Amano N, Narumi S, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T. Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism. Plos One. 7: e46008. PMID 23029363 DOI: 10.1371/Journal.Pone.0046008 |
0.448 |
|
| 2012 |
Mitsui T, Nagasaki K, Takagi M, Narumi S, Ishii T, Hasegawa T. A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus. American Journal of Medical Genetics. Part A. 158: 261-4. PMID 22140064 DOI: 10.1002/Ajmg.A.34393 |
0.394 |
|
| 2005 |
Hashida H, Kuroiwa T, Fukuda T, Inoue K, Yokochi M, Kawamura M, Takagi M, Orimo S, Fujigasaki J. [A case of 51-year-old woman demonstrating akinetic mutism with seven years course of Parkinsonism]. Nå to Shinkei = Brain and Nerve. 57: 425-39. PMID 15981643 |
0.603 |
|
| 2005 |
Mizoi Y, Ida M, Takao M, Koto A, Orimo S, Inoue K, Yokochi M, Kawamura M, Takagi M, Fukuda T, Fujigasaki J. [A case of 53-years-old woman with the onset of subacute right-sided numbness, and presented with various lesions on MRI]. Nå to Shinkei = Brain and Nerve. 57: 333-48. PMID 15948406 |
0.649 |
|
| 2004 |
Amino T, Kanazawa T, Orimo S, Tanaka H, Oka T, Mori S, Takagi M, Inoue K, Yokochi M, Kawamura M, Fukuda T, Fujigasaki J. [A case of 62-year-old man with tumor-like lesion in the brain, presenting with fever and transient consciousness disturbance]. Nō to Shinkei = Brain and Nerve. 56: 617-30. PMID 15379293 |
0.537 |
|
| 2004 |
Ishihara K, Ikeda K, Inoue K, Yokochi M, Kawamura M, Takagi M, Orimo S, Fukuda T, Fujigasaki J. [An autopsy case of 54-year-old man with progressive dementia]. Nō to Shinkei = Brain and Nerve. 56: 439-50. PMID 15279205 |
0.537 |
|
| 2003 |
Yoshioka M, Fujigasaki J, Ohama E, Ida M, Inoue K, Yokochi M, Kawamura M, Takagi M, Orimo S. [An autopsy case of 40-year-old male with encephalitis demonstrated lesions of the cerebral cortex on MRI and presenting symptoms such as delusion and hallucination. Clinical conference]. Nå to Shinkei = Brain and Nerve. 55: 1087-98. PMID 14870580 |
0.536 |
|
| 2003 |
Nagao T, Funata N, Takahashi M, Mori H, Kawamura M, Inoue K, Yokochi M, Takagi M, Orimo S, Fujigasaki J. [A case of fluent aphasia representing severe left temporal lobe atrophy. Clinical conference]. Nō to Shinkei = Brain and Nerve. 55: 1073-85. PMID 14870579 |
0.509 |
|
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