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R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome.
- Published in:
- Neurogenetics, 2018, v. 19, n. 3, p. 179, doi. 10.1007/s10048-018-0552-x
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- Publication type:
- Article
In memoriam: Dr.ssa Anna Maria Valleriani.
- Published in:
- 2014
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- Publication type:
- Obituary
Multidetector CT in diagnostic work-up of patients with primary hyperparathyroidism.
- Published in:
- La Radiologia Medica, 2007, v. 112, n. 5, p. 763, doi. 10.1007/s11547-007-0179-8
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- Publication type:
- Article
Identification of mutations in AP4S1/SPG52 through next generation sequencing in three families.
- Published in:
- European Journal of Neurology, 2016, v. 23, n. 10, p. 1580, doi. 10.1111/ene.13085
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- Publication type:
- Article