1.

Record Nr.

UNINA9910131788003321

Autore

Billard Gérald

Titolo

Ville fermée, ville surveillée : la sécurisation des espaces résidentiels en France et en Amérique du Nord

Pubbl/distr/stampa

Presses universitaires de Rennes, 2005

[Place of publication not identified], : Presses universitaires de Rennes, 2005

ISBN

9782753526761

2753526761

9782821817944

2821817940

Descrizione fisica

1 online resource (235 pages)

Collana

Géographie sociale

Soggetti

Sociology & Social History

Social Sciences

Communities - Urban Groups

Lingua di pubblicazione

Francese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Bibliographic Level Mode of Issuance: Monograph

Nota di bibliografia

Includes bibliographical references.

Sommario/riassunto

La question de la sécurisation des espaces résidentiels en milieu urbain n’est pas nouvelle. Elle se renouvelle sans cesse et deux tendances fortes semblent émerger au cours d’une période récente. La première est l’essor, voire la large diffusion dans certains contextes géographiques, d’enclaves résidentielles fermées destinées non plus seulement et principalement aux catégories aisées mais à destination des classes moyennes, enclave incarnée par la figure désormais banalisée mais assez réductrice de la gated community étatsunienne. La seconde résulte d’une modification des modalités de surveillance de l’espace urbain, sans que celle-ci s’accompagne d’une fermeture territoriale comme dans le cas de l’enclave résidentielle fermée. Cette double tension interroge la façon de vivre en ville et celle de se penser ou de se représenter en société, car au-delà de l’objectif sécuritaire souvent mis en avant mais non exclusif de l’ensemble des processus à l’œuvre, elle traduit fondamentalement une série de transformations



profondes des modes de vie, des relations sociales et des rapports à l’espace. Cette analyse de la sécurisation des espaces résidentiels en milieu urbain, qui oscille entre autoenfermement et surveillance sans fermeture, porte à la fois sur le contexte français et étatsunien.

2.

Record Nr.

UNINA9910300227403321

Autore

Howard Jo

Titolo

Sickle Cell Disease in Clinical Practice / / by Jo Howard, Paul Telfer

Pubbl/distr/stampa

London : , : Springer London : , : Imprint : Springer, , 2015

ISBN

1-4471-2473-1

Edizione

[1st ed. 2015.]

Descrizione fisica

1 online resource (300 p.)

Collana

In Clinical Practice, , 2199-6652

Disciplina

610

615.39

616.07

616.15

Soggetti

Hematology

Pathology

Blood - Transfusion

Blood Transfusion Medicine

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Description based upon print version of record.

Nota di bibliografia

Includes bibliographical references and index.

Nota di contenuto

Overview of Sickle Cell Disease -- Laboratory Tests Used in Diagnosis and Monitoring of Sickle Cell Disease -- Organization of Care for Sickle Cell Disease -- Overview and general principles -- Pain in Sickle Cell Disease -- Respiratory and Cardiac Complications in Sickle Cell Disease -- Neurological Complications of Sickle Cell Disease -- Renal and Urological Complications in Sickle Cell Disease -- Bone and Joint Complications in Sickle Cell Disease -- Ophthalmological complications in Sickle Cell Disease -- The Spleen in Sickle Cell Disease -- Infection and Infection Prophylaxis in Sickle Cell Disease -- Gastroenterological Complications in Sickle Cell Disease -- Anemia and Sickle Cell Disease -- Leg Ulceration in Sickle Cell Disease -- Management of Pregnancy in Sickle Cell Disease -- Surgical Management of Patients with Sickle Cell



Disease -- Sickle Cell Disease Treatment Modalities -- Out-Patient Management of Sickle Cell Disease Patients.

Sommario/riassunto

This practical clinical handbook reveals that sickle cell disease (SCD) is an increasingly common condition to manage in Europe and North America. SCD demands clinical expertise and experience as well as sensitivity to its social and cultural context. This book is designed to broaden readers’ knowledge in this challenging condition by describing the acute and long-term complications unique to SCD and that affect nearly every system of the body. Critically, it also details the significant recent advances in understanding the pathophysiology of SCD that are leading to novel treatment modalities. Sickle Cell Disease in Clinical Practice promotes higher quality care by outlining the clinical problems as they arise, and covering essential background information, including up-to-date research, and useful points to guide management. As such, the intended target audience is broad and includes general physicians, general practitioners, hematologists, pediatricians, emergency medicine physicians, surgeons, medical students, nurse specialists and commissioners.