Results 181 to 190 of about 37,782 (205)

Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria.

Journal of Experimental Medicine, 1987
L S Zalman
exaly  

Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

Movement Disorders, 2018
Wo-Tu Tian, Xiao Mao, Qing Liu
exaly  

Psychogenic paroxysmal movement disorders – Clinical features and diagnostic clues

Parkinsonism and Related Disorders, 2014
Christos Ganos, Amit Batla, Maria Stamelou   +2 more
exaly  

Review: Diagnosis and treatment of paroxysmal dyskinesias revisited

Therapeutic Advances in Neurological Disorders, 2008
Iris Unterberger, Eugen Trinka
exaly  

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Brain, 2000
Enza Maria Valente, Kailash P Bhatia, P H Dixon   +2 more
exaly  

Paroxysmal Supraventricular Tachycardia

New England Journal of Medicine, 1973
openaire   +2 more sources

PRRT2 mutations and paroxysmal disorders

European Journal of Neurology, 2013
Christel Depienne, Emmanuel Roze
exaly  

Paroxysmal dyskinesias revisited: A review of 500 genetically proven cases and a new classification

Movement Disorders, 2014
Roberto Erro, Kailash P Bhatia
exaly  

Paroxysmal Ventricular Tachycardia

Diseases of the Chest, 1961
openaire   +2 more sources

Clinical Practice Guideline: Benign Paroxysmal Positional Vertigo (Update)

Otolaryngology - Head and Neck Surgery, 2017
Seth R Schwartz, Terry Fife, Richard A Roberts   +2 more
exaly