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Publikováno v:
Pediatric Neurosurgery. 1:251-254
The authors have seen eight cases of communicating hydrocephalus in children with genetic metabolic disorders, namely, one mucopolysaccharidosis I (MPS I or Hurler syndrome), one MPS II (Hunter’s disease), four MPS III (Sanfilippo syndrome) two of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96a7f069746d6a05dc986369ef1a25f1
https://doi.org/10.1159/000119574
https://doi.org/10.1159/000119574
