Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Suad Al-Jahdhami"'
Autor:
Roshan Koul, Dilip Sankhla, Suad Al-Jahdhami, Renjith Mani, Rana A. Rahim, Saif Al-Yaarubi, Hussein Al-Kindy, Khalid Al-Thihli, Amna Al-Futaisi
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 364-369 (2015)
Objectives: Rigidity of the spine is common in adults but is rarely observed in children. The aim of this study was to report on rigid spine syndrome (RSS) among children in Oman. Methods: Data on children diagnosed with RSS were collected consecutiv
Externí odkaz:
https://doaj.org/article/65a62381632f4a53b797945b33af3fee
Publikováno v:
Sultan Qaboos University Medical Journal
NONE
Publikováno v:
BMJ. :k3614
A 34 year old woman presented with a 9 day history of progressive proximal bilateral limb weakness and mild dysphagia with fluids. On examination, she had a peri-orbital rash (fig 1). Neurological findings included moderately severe (grade 3-4/5) bil
Autor:
Saif Al-Yaarubi, Roshan Koul, Hussein Al-Kindy, Rana A. Rahim, Suad Al-Jahdhami, Amna Al-Futaisi, Renjith Mani, Dilip Sankhla, Khalid Al-Thihli
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp e364-369 (2015)
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 364-369 (2015)
Sultan Qaboos University Medical Journal, Vol 15, Iss 3, Pp 364-369 (2015)
Objectives: Rigidity of the spine is common in adults but is rarely observed in children. The aim of this study was to report on rigid spine syndrome (RSS) among children in Oman. Methods: Data on children diagnosed with RSS were collected consecutiv
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 17(12)
Rhabdoid meningiomas are rare, aggressive tumours of the meninges that have a generally poor prognosis. We report a 49-year-old man with a background history of sarcoidosis who presented with nausea and vomiting. Imaging showed generalised leptomenin
Autor:
Michael Barnett, Mahtab Ghadiri, Suad Al Jahdhami, Robert Heard, Ian Sutton, Simon Flanagan, Jeffrey Brennan, Michael E. Buckland, Yael Barnett
Publikováno v:
JAMA Neurology. 71:794
A 42-year-old white man presented with cognitive impairment and behavioral changes followed by rapidly progressive motor and gait impairment. Magnetic resonance imaging revealed striking multifocal white matter signal change, areas of restricted diff
Publikováno v:
Pathology. 45:S78
Progressive muscular atrophy (PMA) is the lower motor neuron-predominant form of motor neuron disease (MND). MND is a relatively common, progressive fatal neurodegenerative disease, the pathogenetic basis of which is not fully understood. Recent gene
Autor:
Suad Al-Jahdhami, Jane E. Dahlstrom
Publikováno v:
Pathology. 42:S85
A 33-year-old pregnant woman, G1P0 at 30 weeks gestation, presented to her obstetrician with abdominal tightness associated with fever. On examination, she was febrile (388C) and her full blood count showed leukocytosis with neutrophi-lia. Abdominal