Hemicerebral atrophy as an unusual central nervous system manifestation of Neurofibromatosis type 1: A case report.

Abera B, Belachew B, Ahmed HT, Tefera YD, Amare TZ.

DOI: 10.1016/j.radcr.2026.08.017
Published: 2026-09-07
Container: Radiol Case Rep
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1016/j.radcr.2026.08.017,
  title = {Hemicerebral atrophy as an unusual central nervous system manifestation of Neurofibromatosis type 1: A case report.},
  author = {Abera B and  Belachew B and  Ahmed HT and  Tefera YD and  Amare TZ.},
  year = {2026},
  journal = {Radiol Case Rep},
  doi = {10.1016/j.radcr.2026.08.017},
  url = {https://doi.org/10.1016/j.radcr.2026.08.017}
}

RIS

TY  - JOUR
TI  - Hemicerebral atrophy as an unusual central nervous system manifestation of Neurofibromatosis type 1: A case report.
AU  - Abera B
AU  -  Belachew B
AU  -  Ahmed HT
AU  -  Tefera YD
AU  -  Amare TZ.
PY  - 2026
JO  - Radiol Case Rep
DO  - 10.1016/j.radcr.2026.08.017
UR  - https://doi.org/10.1016/j.radcr.2026.08.017
ER  -

APA

B, A., B, B., HT, A., YD, T., & TZ., A. (2026). Hemicerebral atrophy as an unusual central nervous system manifestation of Neurofibromatosis type 1: A case report.. Radiol Case Rep. https://doi.org/10.1016/j.radcr.2026.08.017

Source records

europe-pmc · retrieved 2026-09-25T08:43:06.892Z
europe-pmc · retrieved 2026-09-25T08:43:06.892Z