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Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2014
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Title
Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatment
Published in
Orphanet Journal of Rare Diseases, July 2014
DOI 10.1186/s13023-014-0105-9
Pubmed ID
Authors

Catia Cavicchi, Maria Alice Donati, Rossella Parini, Miriam Rigoldi, Mauro Bernardi, Francesca Orfei, Nicolò Gentiloni Silveri, Aniello Colasante, Silvia Funghini, Serena Catarzi, Elisabetta Pasquini, Giancarlo la Marca, Sean David Mooney, Renzo Guerrini, Amelia Morrone

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 3%
Canada 1 3%
Unknown 38 95%

Demographic breakdown

Readers by professional status Count As %
Other 9 23%
Researcher 7 18%
Student > Bachelor 4 10%
Student > Ph. D. Student 4 10%
Student > Master 4 10%
Other 4 10%
Unknown 8 20%
Readers by discipline Count As %
Medicine and Dentistry 14 35%
Biochemistry, Genetics and Molecular Biology 5 13%
Agricultural and Biological Sciences 5 13%
Unspecified 2 5%
Physics and Astronomy 1 3%
Other 3 8%
Unknown 10 25%