Your browser doesn't support javascript.
loading
Late diagnosis of hypophosphatasia in a case with Unverricht-Lundborg disease.
Zouwail, Soha; Longworth, Nathan; Grey, Joseph; Nesbitt, Mandy; Sisodiya, Sanjay; Hamandi, Khalid.
Affiliation
  • Zouwail S; 1 Department of Biochemistry & Immunology, University Hospital of Wales, Cardiff, UK.
  • Longworth N; 2 Department of Medical Biochemistry, School of Medicine, Alexandria University, Alexandria, Egypt.
  • Grey J; 3 Department of Gerontology, University Hospital of Wales, Cardiff, UK.
  • Nesbitt M; 3 Department of Gerontology, University Hospital of Wales, Cardiff, UK.
  • Sisodiya S; 4 Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
  • Hamandi K; 5 UCL Institute of Neurology, UCL, London, UK.
Ann Clin Biochem ; 56(4): 515-518, 2019 07.
Article in En | MEDLINE | ID: mdl-31088113

Full text: 1 Database: MEDLINE Main subject: Unverricht-Lundborg Syndrome / Alkaline Phosphatase / Hypophosphatasia / Anticonvulsants Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Unverricht-Lundborg Syndrome / Alkaline Phosphatase / Hypophosphatasia / Anticonvulsants Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Year: 2019 Type: Article