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Titlebook: Medical and Surgical Complications of Sickle Cell Anemia; Ahmed Al-Salem Book 2016 Springer International Publishing Switzerland 2016 Acut

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發(fā)表于 2025-3-21 17:37:33 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Medical and Surgical Complications of Sickle Cell Anemia
編輯Ahmed Al-Salem
視頻videohttp://file.papertrans.cn/630/629413/629413.mp4
概述Aids in the diagnosis and management of a wide range of complications.Presented in a bullet point format that makes the book an ideal quick reference.Includes numerous high-quality illustrations
圖書封面Titlebook: Medical and Surgical Complications of Sickle Cell Anemia;  Ahmed Al-Salem Book 2016 Springer International Publishing Switzerland 2016 Acut
描述.This book is a wide-ranging guide to the diagnosis and management of the numerous medical and surgical complications that may arise in patients with sickle cell anemia. After introductory chapters on the genetics, pathophysiology, clinical features, and variants of sickle cell anemia, the complications observed in different parts of the body are addressed in a series of well-illustrated chapters. The coverage includes splenic, hepatobiliary, musculoskeletal, gastrointestinal, ophthalmological, cardio- and cerebrovascular, and renal complications, as well as acute chest syndrome, leg ulcers, hand and foot syndrome, acute appendicitis, and priapism. Treatment-oriented chapters consider perioperative management, blood transfusion therapy, hydroxyurea treatment, hematopoietic stem cell transplantation, and emerging strategies. The book is clearly written in a distinctive bullet point format for ease of reference and emphasizes especially aspects of practical significance. It will be ofvalue for hematologists, general surgeons, internists, pediatricians, pediatric surgeons, fellows, residents, medical students, and nurses.?.
出版日期Book 2016
關(guān)鍵詞Acute Chest Syndrome; Cholelithiasis; Medical Complications; Sickle Cell Anemia; Splenic Complications; S
版次1
doihttps://doi.org/10.1007/978-3-319-24762-5
isbn_softcover978-3-319-79673-4
isbn_ebook978-3-319-24762-5
copyrightSpringer International Publishing Switzerland 2016
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 22:24:46 | 只看該作者
Book 2016sickle cell anemia. After introductory chapters on the genetics, pathophysiology, clinical features, and variants of sickle cell anemia, the complications observed in different parts of the body are addressed in a series of well-illustrated chapters. The coverage includes splenic, hepatobiliary, mus
板凳
發(fā)表于 2025-3-22 04:08:33 | 只看該作者
地板
發(fā)表于 2025-3-22 06:11:42 | 只看該作者
Genetics and Pathophysiology of Sickle Cell Anemia,The normal hemoglobin is made up of two parts, heme and protein. The protein is made up of four polypeptide chains (Fig. 2.1):
5#
發(fā)表于 2025-3-22 12:03:29 | 只看該作者
Variants of Sickle Cell Anemia,The normal hemoglobin is made up of two parts (Fig. 3.1):
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發(fā)表于 2025-3-22 16:03:55 | 只看該作者
The Spleen and Sickle Cell Anemia,The word spleen comes from the Greek σπλ?ν (.) and is the idiomatic equivalent of the heart in English, i.e., to be good-spleened (ε?σπλαγχνο?, .) means to be good-hearted or compassionate.
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發(fā)表于 2025-3-22 19:23:15 | 只看該作者
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發(fā)表于 2025-3-23 00:40:16 | 只看該作者
The Acute Chest Syndrome in Sickle Cell Anemia,Acute chest syndrome (ACS) is defined as a new infiltrate on chest X-ray that is associated with one or more of the following symptoms:
9#
發(fā)表于 2025-3-23 04:43:58 | 只看該作者
Musculoskeletal Manifestations of Sickle Cell Anemia,One of the common manifestations of sickle cell anemia is vaso-occlusive crises which affect virtually all patients with sickle cell anemia.
10#
發(fā)表于 2025-3-23 06:21:05 | 只看該作者
Gastrointestinal Complications of Sickle Cell Anemia,Sickle cell anemia is one of the most common inherited hemoglobinopathies worldwide.
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