Annals of Child Neurology

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RANBP2 Mutation in a Child with Recurrent Acute Necrotizing Encephalopathy

Sung Hye Park, Dong Hyun Kim, Young Se Kwon

Ann Child Neurol. 2020;28(2):66-68. Published online January 31, 2020
DOI: https://doi.org/10.26815/acn.2019.00213

RANBP2 Mutation in a Child with Recurrent Acute Necrotizing Encephalopathy

Sung Hye Park, Dong Hyun Kim, Young Se Kwon

Annals of Child Neurology. 2020;28(2):66-68

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RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathy

Vishal Sondhi, Biswaroop Chakrabarty, Atin Kumar, Sudha Kohli, Renu Saxena, I.C. Verma, Sheffali Gulati

Brain and Development. 2016;38(10):937-942

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P298 Steroid-responsive recurrent familial acute necrotizing encephalopathy caused by RANBP2 mutation

Th. Schmitt-Mechelke

European Journal of Paediatric Neurology. 2009;13:S114

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Acute Necrotizing Encephalopathy: 2 Case Reports on RANBP2 Mutation

Molly Hartley, Anjana Sinha, Ashutosh Kumar, Ermal Aliu, Gayatra Mainali, Sita Paudel

Child Neurology Open. 2021;8:2329048X2110307

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Outcomes in influenza and RANBP2 mutation‐associated acute necrotizing encephalopathy of childhood

Nurin Chatur, Carmen Yea, Birgit Ertl‐Wagner, E. Ann Yeh

Developmental Medicine & Child Neurology. 2022;64(8):1008-1016

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RANBP2 Mutation in Clinically Undiagnosed Acute Necrotizing Encephalopathy

Sedat Işıkay, Yavuz Şahin

The Indian Journal of Pediatrics. 2018;85(9):820-821

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First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype

Akif Ayaz, Zeynep Doğru, Betül Kılıç, Barış Ethem Süzek

Clinical Neurology and Neurosurgery. 2022;221:107418

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P249 Recurrent episodes of acute necrotizing encephalopathy caused by a mutation in a component of the nuclear pore, RANBP2

S. Mastroyianni, A. Skardoutsou, K. Voudris, E. Katsarou, J. Nikas, V. Spoulou, D. Gionnis, D. Neilson

European Journal of Paediatric Neurology. 2009;13:S98-S99

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Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

Esra Sarigecili, Habibe Koc Ucar, Cengiz Havali, Ali Cansu, Kursad Aydin

Acta Neurologica Belgica. 2022;

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Familial acute necrotizing encephalopathy without RANBP2 mutation: Poor outcome

Naoko Nishimura, Yoshihisa Higuchi, Nobusuke Kimura, Fumihito Nozaki, Tomohiro Kumada, Ai Hoshino, Makiko Saitoh, Masashi Mizuguchi

Pediatrics International. 2016;58(11):1215-1218

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