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You searched for: Author/Creator Di Rocco, Federico

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1. Cerebellar lesions at a young age predict poorer long-term functional recovery. Issue 1 (6th March 2020)

2. Expanding the phenotype in Adams–Oliver syndrome correlating with the genotype. Issue 1 (25th October 2019)

3. Germline mutations in FGF receptors and medulloblastomas12. Issue 2 (16th January 2013)

4. High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR). (20th November 2018)

5. Human Foramen Magnum Area and Posterior Cranial Fossa Volume Growth in Relation to Cranial Base Synchondrosis Closure in the Course of Child Development. Issue 5 (23rd June 2016)

6. Human Foramen Magnum Area and Posterior Cranial Fossa Volume Growth in Relation to Cranial Base Synchondrosis Closure in the Course of Child Development. Issue 5 (November 2016)

7. Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations. Issue 2 (14th October 2009)

8. Magnetic resonance imaging is a valuable tool to evaluate the therapeutic efficacy of burosumab in children with X-linked hypophosphatemia. Issue 4 (27th August 2021)

9. Moyamoya syndrome in children with neurofibromatosis type 1: Italian–French experience. Issue 6 (19th April 2017)