東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

FindBook

Google Book

Amazon

博客來

Atlas of common and rare genodermatoses

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Atlas of common and rare genodermatoses/ by Nayera Moftah ... [et al.].
其他作者:	Moftah, Nayera.
出版者:	Cham :Springer Nature Switzerland : : 2024.,
面頁冊數:	xiv, 265 p. :ill. (chiefly color), digital ;24 cm.
內容註:	Preface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.
Contained By:	Springer Nature eBook
標題:	Skin - Atlases. - Diseases -
電子資源:	https://doi.org/10.1007/978-3-031-60788-2
ISBN:	9783031607882

Atlas of common and rare genodermatoses
Atlas of common and rare genodermatoses[electronic resource] /by Nayera Moftah ... [et al.]. - Cham :Springer Nature Switzerland :2024. - xiv, 265 p. :ill. (chiefly color), digital ;24 cm.

Preface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.

The management of cutaneous findings in genodermatoses is challenging to the practicing clinician, especially when all hues of skin and skin types are contemplated, and first-line therapies often inadequate. This carefully crafted Atlas includes all sorts of different ethnic skin types, while featuring a wealth of over 1000 commented images collected in more than a decade, including 200 rare genodermatoses, and providing the reader with key points for correct dermatological diagnosis. The contents start with disorders of keratinization and pigmentation, as well as bullous, acantholytic, dermal, hair and nail diseases. Successively, immunodeficiency syndromes and their skin related symptoms, hamartoneoplastic syndromes and defective excision repair syndromes are presented. The addition of vascular disorders, as well as syndromes with premature aging grant full topic coverage. This Atlas of Common and Rare Genodermatoses will be a valued companion to dermatologists and paediatric specialists in their daily practice.

ISBN: 9783031607882

Standard No.: 10.1007/978-3-031-60788-2doiSubjects--Topical Terms:

3733859
Skin
--Diseases--Atlases.

LC Class. No.: RL793

Dewey Class. No.: 616.5042

Atlas of common and rare genodermatoses
LDR:02360nmm a2200325 a 4500 001 2380422
003 DE-He213
005 20241023125755.0
006 m d
007 cr nn 008maaau
008 250418s2024 sz s 0 eng d
020 $a 9783031607882 $q (electronic bk.)
020 $a 9783031607875 $q (paper)
024 7 $a 10.1007/978-3-031-60788-2 $2 doi
035 $a 978-3-031-60788-2
040 $a GP $c GP
041 0 $a eng
050 4 $a RL793
072 7 $a MJK $2 bicssc
072 7 $a MED017000 $2 bisacsh
072 7 $a MJK $2 thema
082 0 4 $a 616.5042 $2 23
090 $a RL793 $b .A881 2024
245 0 0 $a Atlas of common and rare genodermatoses $h [electronic resource] / $c by Nayera Moftah ... [et al.].
260 $a Cham : $b Springer Nature Switzerland : $b Imprint: Springer, $c 2024.
300 $a xiv, 265 p. : $b ill. (chiefly color), digital ; $c 24 cm.
505 0 $a Preface -- I. Disorders of keratinization -- II. Disorders of pigmentation -- III. Acantholytic disorders -- IV. Dermal disorders -- V. Disorders of hair and nail -- VI. Syndromes with immunodeficiency -- VII. Hamartoneoplastic syndromes -- VIII. Syndromes with defective excision repair -- IX. Syndromes with vascular disorders -- X. Syndromes with premature aging.
520 $a The management of cutaneous findings in genodermatoses is challenging to the practicing clinician, especially when all hues of skin and skin types are contemplated, and first-line therapies often inadequate. This carefully crafted Atlas includes all sorts of different ethnic skin types, while featuring a wealth of over 1000 commented images collected in more than a decade, including 200 rare genodermatoses, and providing the reader with key points for correct dermatological diagnosis. The contents start with disorders of keratinization and pigmentation, as well as bullous, acantholytic, dermal, hair and nail diseases. Successively, immunodeficiency syndromes and their skin related symptoms, hamartoneoplastic syndromes and defective excision repair syndromes are presented. The addition of vascular disorders, as well as syndromes with premature aging grant full topic coverage. This Atlas of Common and Rare Genodermatoses will be a valued companion to dermatologists and paediatric specialists in their daily practice.
650 0 $a Skin $x Diseases $x Genetic aspects $v Atlases. $3 3733859
650 1 4 $a Dermatology. $3 829009
650 2 4 $a Pediatrics. $3 559143
650 2 4 $a Immunological Disorders. $3 3603441
650 2 4 $a Diagnosis. $3 707211
700 1 $a Moftah, Nayera. $3 3733858
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer Nature eBook
856 4 0 $u https://doi.org/10.1007/978-3-031-60788-2
950 $a Medicine (SpringerNature-11650)