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期刊名:Archives of neurology

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ISSN:0003-9942

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共收录本刊相关文章索引10579
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
José L Ruiz-Sandoval,Víctor García-Navarro,Erwin Chiquete et al. José L Ruiz-Sandoval et al.
Background: Choreoacanthocytosis (CHAC) (Online Mendelian Inheritance in Man accession No. 200150) is a hereditary neurodegenerative syndrome characterized by movement disorders, cognitive decline, myopathy, behavioral ch...
Marcus Yountz,Manu Mehdiratta,Louis R Caplan Marcus Yountz
Objective: To describe a patient with a predominantly unilateral intracranial arterial stenosis who then developed metastatic lung cancer to the brain, with the tumors preferentially depositing in the underperfused cerebr...
Jung Han Yoon,Phil Hyu Lee,Suk Nam Yoon Jung Han Yoon
Background: Paroxysmal exercise-induced dystonia is a rare hyperkinetic disease characterized by episodic dystonic attacks after prolonged exercise. However, its pathophysiological and anatomical basis are poorly understo...
Elan D Louis,Nicole Schupf,Ming X Tang et al. Elan D Louis et al.
Objective: To determine whether plasma homocysteine (Hcy) concentration is associated with mild parkinsonian signs (MPS) in community-dwelling elderly individuals. ...
Uwe Walter,Dirk Dressler,Thomas Probst et al. Uwe Walter et al.
Background: In several pilot studies, transcranial brain sonography findings of substantia nigra and lenticular nucleus discriminated between idiopathic Parkinson disease (PD) and atypical parkinsonian disorders. ...
An C M Jansen,Henian Cao,Paige Kaplan et al. An C M Jansen et al.
Background: Mucopolysaccharidosis type IIID (MPS-IIID), or Sanfilippo syndrome type D, is a rare autosomal recessive lysosomal storage disorder caused by mutations in the N-acetylglucosamine-6-sulfatase (GNS) gene, leadin...