R Fallows, K McCoy, J Hertza… - Archives of Clinical …, 2011 - acn.oxfordjournals.org Objective: The seminal paper on cerebellar cognitive affective syndrome by Schmahmann and Sherman (1998), and sub- sequent studies, has expanded our understanding of the role of the cerebellum beyond motor functioning to psychological and cognitive functioning. ...
R Mori, S Vasavada, D Baker… - Urology, 2011 - ncbi.nlm.nih.gov OBJECTIVE: To describe the surgical technique of botulinum-A toxin injection into the cremasteric muscles of a 26-year-old male with bilateral cremasteric muscle spasms causing significant pain and limitation of activity. This pain has been refractory to multiple previous therapies, ... All 4 versions
A Ishiyama, Y Saito, K Sugai, M Sasaki… - Brain and …, 2011 - Elsevier We report the case of a 5-year-old boy with multiple congenital anomalies, including ptosis, polydactyly, ventricular septal defect, epilepsy, and intellectual deficits. The patient presented with synkinetic eyelid movements accompanying jaw and ocular movements, ... Related articles - All 3 versions
ME Geffner - Chronic Complex Diseases of Childhood: A …, 2011 - books.google.com ... earlier diagnosis. All patients with Kallmann syndrome have either hyposmia or anosmia, and may also exhibit unilateral renal agenesis, atrial septal defect, colorblindness, and synkinesia (mirror movements). Clinical course ... Related articles
MG Au, WF Crowley Jr… - Molecular and Cellular Endocrinology, 2011 - Elsevier ... features typical of KAL1. The proband, indicated by the arrow, has synkinesia in addition to his anosmic IGD, and carries a R191X mutation on the KAL1 gene on his X chromosome and a normal Y chromosome. His maternal uncle ...
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