Francomano CA

No ORCID on file · 2 papers in corpus
2024
Neurosurgical review ·doi:10.1007/s10143-023-02249-0

Craniocervical instability (CCI) is increasingly recognized in hereditary disorders of connective tissue and in some patients following suboccipital decompression for Chiari malformation (CMI) or low-lying cerebellar tonsils (LLCT). CCI is …

2020
Orphanet journal of rare diseases ·doi:10.1186/s13023-020-01468-8

Alström Syndrome (ALMS) is an ultra-rare multisystem genetic disorder caused by autosomal recessive variants in the ALMS1 gene, which is located on chromosome 2p13. ALMS is a multisystem, progressive disease characterised by visual disturba…