Vendor Profile
Osaka University Press
| Address | Osaka University West Front Ymadaoka2-7 Suita-shi Osaka, JAPAN ZIP:565-0871 |
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| Representative Name | MITSUNARI KENJI |
| Annual Revenue | closed |
| No. of Employees | 7 |
| Web Site URL | |
| SNS |
SD item code:10939495
| Detail | Price & Quantity | ||
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| S1 |
Rett Syndrome Medical Guidebook
 Original text before translation
レット症候群診療ガイドブック
(978-4-87259-496-6)
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(978-4-87259-496-6)
Wholesale Price: Members Only
1 pc /set
In Stock
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| Shipping Date |
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About 10 days
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| Dimensions |
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A5 size, 254 pages
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| Specifications |
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Country of manufacture: Japan
Material / component: Paper
Package: Individual Packaging
Year of manufacture: 2015
Product tag: None
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Description
| Makoto Aotame (editor), Masayuki Ito (editor) To diagnose as early as possible and to program symptomatic methods including rehabilitation and education. To all staff involved in the diagnosis and treatment of Rett syndrome. The difficulty of diagnosis is expected to gradually change due to the revised diagnostic criteria developed in the studies that have been conducted since the discovery of the main causative gene, MECP2, which was reported in 1999. The Ministry of Health, Labour and Welfare [Rett Syndrome] Research Group has compiled an overview, description of common symptoms, symptomatic methods, social welfare resources, and expected future treatment from the results of its research. |
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| Shipping Method | Estimated Arrival |
|---|---|
| Sea Mail | From Dec.11th 2025 to Feb.12th 2026 |
| Air Mail | From Nov.25th 2025 to Nov.27th 2025 |
| EMS | From Nov.24th 2025 to Nov.27th 2025 |
| Pantos Express | From Nov.26th 2025 to Dec.1st 2025 |
| DHL | From Nov.24th 2025 to Nov.26th 2025 |
| UPS | From Nov.24th 2025 to Nov.26th 2025 |
| FedEx | From Nov.24th 2025 to Nov.26th 2025 |
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Some trading conditions may be applicable only in Japan. |
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To diagnose as early as possible and to program symptomatic methods including rehabilitation and education. To all staff involved in the diagnosis and treatment of Rett syndrome. The difficulty of diagnosis is expected to gradually change due to the revised diagnostic criteria developed in the studies that have been conducted since the discovery of the main causative gene, MECP2, which was reported in 1999. The Ministry of Health, Labour and Welfare [Rett Syndrome] Research Group has compiled an overview, description of common symptoms, symptomatic methods, social welfare resources, and expected future treatment from the results of its research.