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10.1186/s40673-018-0085-y http://scihub22266oqcxt.onion/10.1186/s40673-018-0085-y C5861599!5861599!29568536     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Cerebellum+Ataxias 2018 ; 5 (ä): ä Nephropedia Template TP {{tp|p=29568536|t=2018. Cerebellar cognitive affective syndrome: insights from Joubert syndrome |pdf=|usr=}}{{29568536}} gab.com Text Cerebellar cognitive affective syndrome: insights from Joubert syndrome JO: Cerebellum Ataxias http://www.kidney.de/pget.php?&tw=1&pmid=29568536 #FOAvip Background: Joubert syndrome (JS) is a rare, autosomal recessively inherited genetic disorder characterized morphologically by unique developmental malformations of the cerebellum and brainstem (the molar tooth sign), and clinically by impaired motor functions and intellectual disability. Patients with JS often face multiple cognitive challenges, but the neuropsychological profile of this condition has not been well characterized. Methods: We performed comprehensive neurological and neuropsychological evaluations in three adult brothers with JS, ages 32, 27, and 25 years. Results: They all exhibited impaired motor control, global developmental delay most evident in executive function, affect regulation, and social skill set, and similar patterns of neuropsychiatric symptoms. Conclusions: These findings provide new insights into the intellectual and neurobehavioral phenotype of JS, which we regard as a developmental form of the cerebellar cognitive affective / Schmahmann syndrome (CCAS). These observations have direct clinical relevance for the diagnosis and care of patients with JS, and they help further the understanding of the multiple manifestations of atypical cerebrocerebellar development. Twit Text FOAVip Cerebellar cognitive affective syndrome: insights from Joubert syndrome ????Cerebellum Ataxias http://www.kidney.de/pget.php?&tw=1&pmid=29568536 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29568536 #FOAvip English Wikipedia <ref>{{Cite pmid|29568536}}</ref> Cerebellar cognitive affective syndrome: insights from Joubert syndrome #MMPMID29568536 Hickey CL; Sherman JC; Goldenberg P; Kritzer A; Caruso P; Schmahmann JD; Colvin MK Cerebellum Ataxias 2018[]; 5 (ä): ä PMID29568536show ga Background: Joubert syndrome (JS) is a rare, autosomal recessively inherited genetic disorder characterized morphologically by unique developmental malformations of the cerebellum and brainstem (the molar tooth sign), and clinically by impaired motor functions and intellectual disability. Patients with JS often face multiple cognitive challenges, but the neuropsychological profile of this condition has not been well characterized. Methods: We performed comprehensive neurological and neuropsychological evaluations in three adult brothers with JS, ages 32, 27, and 25 years. Results: They all exhibited impaired motor control, global developmental delay most evident in executive function, affect regulation, and social skill set, and similar patterns of neuropsychiatric symptoms. Conclusions: These findings provide new insights into the intellectual and neurobehavioral phenotype of JS, which we regard as a developmental form of the cerebellar cognitive affective / Schmahmann syndrome (CCAS). These observations have direct clinical relevance for the diagnosis and care of patients with JS, and they help further the understanding of the multiple manifestations of atypical cerebrocerebellar development. äCerebellar cognitive affective syndrome: insights from Joubert syndrom(epmc).pdf DeepDyve Pubget Overpricing