Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy-Reference-Cited by-同舟云学术

Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy

Published:2010 Issue:11 Volume:57 Page:965-972
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Miyoshi Yoko¹,Sakai Norio¹,Hamada Yusuke¹,Tachibana Makiko¹,Hasegawa Yasuhiro¹,Kiyohara Yuki¹,Yamada Hiroyuki¹,Murakami Mari¹,Kondou Hiroki¹,Kimura-Ohba Shihoko¹,Mine Junji²,Sato Tatsuharu³,Kamio Noriko⁴,Ueda Hitoshi⁵,Suzuki Yasuhiro⁶,Shiomi Masashi⁷,Ohta Hideaki¹,Shimozawa Nobuyuki⁸,Ozono Keiichi¹

Affiliation:

1. Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan

2. Department of Pediatrics, Hyogo College of Medicine, Hyogo, Japan

3. Department of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan

4. Department of Pediatrics, Itami Municipal Hospital, Osaka, Japan

5. Department of Pediatrics, Osaka General Medical Center, Osaka, Japan

6. Division of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan

7. Department of Pediatric Emergent Medicine and Infectious Disease Center, Osaka City General Hospital, Osaka, Japan

8. Division of Genomics Research, Life Science Research Center, Gifu University, Gifu, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj/57/11/57_K10E-204/_pdf

Reference32 articles.

1. 1. Moser HW, Mahmood A, Raymond GV (2007) X-linked adrenoleukodystrophy. Nat Clin Pract Neurol 3:140-151.

2. FATTY ACID ABNORMALITY IN ADRENOLEUKODYSTROPHY

3. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

4. 5. Moser HW, Loes DJ, Melhem ER, Raymond GV, Bezman L, Cox CS, Lu SE (2000) X-linked adrenoleukodystrophy: overview and prognosis as a function of age and brain magnetic resonance imaging abnormality: a study involving 372 patients. Neuropediatrics 31: 227-239.

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