✦ LIBER ✦

SPECIFICITY OF THE REPRESENTATION OF THEIR OWN ILLNESS BY PATIENTS WITH SCHIZOPHRENIA HAVING BEEN INFORMED OF THEIR DIAGNOSIS

✍ Scribed by Elisabeth Bacon; Alexandra Herbay

Book ID: 119557227
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 57 KB
Volume: 102
Category: Article
ISSN: 0920-9964
DOI: 10.1016/s0920-9964(08)70405-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1153-68 Do patients with heart failure h

1153-68 Do patients with heart failure have a medically accurate mental image of their illness (also known as illness representation)?

✍ Nancy M Albert 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 68 KB

Needs for care of patients with schizoph

Needs for care of patients with schizophrenia and the consequences for their informal caregivers

✍ Karin Meijer; Aart Schene; Maarten Koeter; HelleCharlotte Knudsen; Thomas Becker 📂 Article 📅 2004 🏛 Springer-Verlag 🌐 English ⚖ 238 KB

Patient knowledge of their own illness:

Patient knowledge of their own illness: How much does it matter and how may we adapt our information to what the patient knows?

✍ Peter J. Schulz; Arnstein Finset 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 107 KB

The Association of Type 2 Diabetes Patie

The Association of Type 2 Diabetes Patient and Spouse Illness Representations with Their Well-being: A Dyadic Approach

✍ Georgia Dimitraki, Evangelos C. Karademas 📂 Article 📅 2013 🏛 Springer US 🌐 English ⚖ 266 KB

An international survey on information n

An international survey on information needs of patients with schizophrenia and their carers and management issues most frequently encountered by professional care team members

✍ T. Wærner; M. Bassi; J. Dubuis; W.W. Fleischhacker; W. Kissling; D. Linszen; G. 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 155 KB

Novel mutations of the GLA gene in Japan

Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone

✍ Masaaki Shimotori; Hiroki Maruyama; Gen Nakamura; Takayuki Suyama; Fumiko Sakamo 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 613 KB

Fabry disease is an X-linked recessive inborn metabolic disorder caused by a deficiency of the lysosomal enzyme alpha-galactosidase A (EC 3.2.1.22). The causative mutations are diverse, include both large rearrangements and single-base substitutions, and are dispersed throughout the 7 exons of the a