Literature DB >> 23045520

Child Neurology: a case of PMM2-CDG (CDG 1a) presenting with unusual eye movements.

Rohini Coorg1, Timothy E Lotze.   

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Year:  2012        PMID： 23045520     DOI： 10.1212/WNL.0b013e31826e2617

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  1 in total

1.  Clinical and radiological correlates of activities of daily living in cerebellar atrophy caused by PMM2 mutations (PMM2-CDG).

Authors:  Fabio Pettinato; Giovanni Mostile; Roberta Battini; Diego Martinelli; Annalisa Madeo; Elisa Biamino; Daniele Frattini; Domenico Garozzo; Serena Gasperini; Rossella Parini; Fabio Sirchia; Giuseppe Sortino; Luisa Sturiale; Gert Matthijs; Amelia Morrone; Maja Di Rocco; Renata Rizzo; Jaak Jaeken; Agata Fiumara; Rita Barone
Journal:  Cerebellum       Date:  2021-02-22       Impact factor: 3.847
  1 in total

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