Issue Navigation
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Review
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165-169
The role of L-type amino acid transporter 1 in human tumors.
Zhao Y, Wang L, Pan JH
Intractable Rare Dis Res. 2015; 4(4):165-169.
DOI: 10.5582/irdr.2015.01024
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170-180
Sarcoidosis and the heart: A review of the literature.
Ipek E, Demirelli S, Ermis E, Inci S
Intractable Rare Dis Res. 2015; 4(4):170-180.
DOI: 10.5582/irdr.2015.01023
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181-189
Sato Y, Nakatani E, Watanabe Y, Fukushima M, Nakashima K, Kannagi M, Kanatani Y, Mizushima H
Intractable Rare Dis Res. 2015; 4(4):181-189.
DOI: 10.5582/irdr.2015.01043
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190-197
Multiplex cytokine analysis of Werner syndrome.
Goto M, Hayata K, Chiba J, Matsuura M, Iwaki-Egawa S, Watanabe Y
Intractable Rare Dis Res. 2015; 4(4):190-197.
DOI: 10.5582/irdr.2015.01035
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198-202
Identification of a male with fragile X syndrome through newborn screening.
Famula J, Basuta K, Gane LW, Hagerman RJ, Tassone F
Intractable Rare Dis Res. 2015; 4(4):198-202.
DOI: 10.5582/irdr.2015.01031
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203-206
An isolated single L-II type coronary artery anomaly: A rare coronary anomaly.
Ermis E, Demirelli S, Korkmaz AF, Dilekci Sahin B, Kantarci A
Intractable Rare Dis Res. 2015; 4(4):203-206.
DOI: 10.5582/irdr.2015.01025
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207-209
Azathioprine-induced atrial fibrillation.
Dogan P, Grbovic E, Inci S, Bayraktar F, Cagli K
Intractable Rare Dis Res. 2015; 4(4):207-209.
DOI: 10.5582/irdr.2015.01033
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210-213
Infantile systemic hyalinosis in identical twins.
Mahesh Kumar. K, Satya Prasad. V
Intractable Rare Dis Res. 2015; 4(4):210-213.
DOI: 10.5582/irdr.2015.01027
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214-216
Nailfold capillaroscopic changes in Kindler syndrome.
Dobrev H, Vutova N
Intractable Rare Dis Res. 2015; 4(4):214-216.
DOI: 10.5582/irdr.2015.01038
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217-219
Lu HZ
Intractable Rare Dis Res. 2015; 4(4):217-219.
DOI: 10.5582/irdr.2015.01032