✦ LIBER ✦

The neuroleptic malignant syndrome: Review and report of three cases

✍ Scribed by Lawrence B. Greenberg; Krishnareddy Gujavarty

Book ID: 115841747
Publisher: Elsevier Science
Year: 1985
Tongue: English
Weight: 543 KB
Volume: 26
Category: Article
ISSN: 1532-8384
DOI: 10.1016/0010-440x(85)90050-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Neuroleptic Malignant Syndrome and Sever

Neuroleptic Malignant Syndrome and Severe Thrombocytopenia: Case Report and Literature Review

✍ Shareh O. Ghani; Waqas Ahmed; Luis A. Marco 📂 Article 📅 2000 🏛 American Academy of Clinical Psychiatrists 🌐 English ⚖ 43 KB

The neuroleptic malignant syndrome : Cas

The neuroleptic malignant syndrome : Case report with a review of the literature

✍ P. ALLSOP; A. J. TWIGLEY 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 401 KB

Abortive forms of the neuroleptic malign

Abortive forms of the neuroleptic malignant syndrome: Four case reports

✍ O. Zivanovic; Lj. Borisev; V. Borisev 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 372 KB

Rare neuropsychiatric sequelae following

Rare neuropsychiatric sequelae following neuroleptic malignant syndrome: A case report and review of the literature

✍ Lai Gwen Chan; Jimmy Lee; Boon Tat Ng; Ee Lian Lee; Hong Choon Chua; Kang Sim 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 119 KB

Clozapine Withdrawal Catatonia and Neuro

Clozapine Withdrawal Catatonia and Neuroleptic Malignant Syndrome: A Case Report

✍ Joseph W. Y. Lee; Stephen Robertson 📂 Article 📅 1997 🏛 American Academy of Clinical Psychiatrists 🌐 English ⚖ 461 KB

W syndrome: Report of three cases and re

W syndrome: Report of three cases and review

✍ Goizet, Cyril; Bonneau, Dominique; Lacombe, Didier 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 25 KB 👁 2 views

Only three cases of W syndrome have been reported. These patients have a typical "pugilistic" face, incomplete oral cleft, absent upper incisors, mental retardation, spasticity, seizures, and acne scars. Two of them had additional skeletal anomalies. Here we report on three male patients with findin