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Abstract

Spontaneous involution of optic pathway lesions in neurofibromatosis type 1: serial contrast MR evaluation.

C Parazzini, F Triulzi, E Bianchini, V Agnetti, M Conti, C Zanolini, M M Maninetti, L N Rossi and G Scotti
American Journal of Neuroradiology September 1995, 16 (8) 1711-1718;
C Parazzini
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F Triulzi
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E Bianchini
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V Agnetti
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M Conti
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C Zanolini
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M M Maninetti
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L N Rossi
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G Scotti
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Article Information

vol. 16 no. 8 1711-1718
PubMed 
7502979

Published By 
American Journal of Neuroradiology
Print ISSN 
0195-6108
Online ISSN 
1936-959X
History 
  • Published online September 1, 1995.

Copyright & Usage 
Copyright © American Society of Neuroradiology

Author Information

  1. C Parazzini,
  2. F Triulzi,
  3. E Bianchini,
  4. V Agnetti,
  5. M Conti,
  6. C Zanolini,
  7. M M Maninetti,
  8. L N Rossi and
  9. G Scotti
  1. Department of Neuroradiology, Scientific Institute H.S. Raffaele, University of Milan, Italy.

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American Journal of Neuroradiology
Vol. 16, Issue 8
1 Sep 1995
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Cite this article
C Parazzini, F Triulzi, E Bianchini, V Agnetti, M Conti, C Zanolini, M M Maninetti, L N Rossi, G Scotti
Spontaneous involution of optic pathway lesions in neurofibromatosis type 1: serial contrast MR evaluation.
American Journal of Neuroradiology Sep 1995, 16 (8) 1711-1718;

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Spontaneous involution of optic pathway lesions in neurofibromatosis type 1: serial contrast MR evaluation.
C Parazzini, F Triulzi, E Bianchini, V Agnetti, M Conti, C Zanolini, M M Maninetti, L N Rossi, G Scotti
American Journal of Neuroradiology Sep 1995, 16 (8) 1711-1718;
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Cited By...

  • Optic Pathway Glioma and Cerebral Focal Abnormal Signal Intensity in Patients with Neurofibromatosis Type 1: Characteristics, Treatment Choices and Follow-up in 134 Affected Individuals and a Brief Review of the Literature
  • Juvenile pilocytic astrocytomas do not undergo spontaneous malignant transformation: grounds for designation as hamartomas
  • Pilocytic astrocytomas as hamartomas: implications for treatment
  • Optic Pathway Glioma: Correlation of Imaging Findings with the Presence of Neurofibromatosis
  • Prospective Evaluation of the Brain in Asymptomatic Children with Neurofibromatosis Type 1: Relationship of Macrocephaly to T1 Relaxation Changes and Structural Brain Abnormalities
  • MRI and clinical differences between optic pathway tumours in children with and without neurofibromatosis
  • Malignancy in Neurofibromatosis Type 1
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Print ISSN: 0195-6108 Online ISSN: 1936-959X

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