Page 61 - Demo

Parkinsonism in GNDs592Alagille*[tiab] OR Alagille syndrome*[tiab] OR Arteriohepatic Dysplasia*[tiab] OR Cardiovertebral Syndrome*[tiab] OR Arteriohepatic Dysplasia*[tiab] OR Watson miller syndrome*[tiab] OR Hepatic Ductular Hypoplasia*[tiab] OR alagille-watson*[tiab] OR “CHARGE Syndrome”[Mesh] OR CHARGE syndrome*[tiab] OR hall hittner syndrome*[tiab] OR Charge association*[tiab] OR “Costello Syndrome”[Mesh] OR Costello syndrome*[tiab] OR FCS syndrome*[tiab] OR Faciocutaneoskeletal Syndrome*[tiab] OR “Genetic Diseases, X-Linked”[Mesh] OR X-linked genetic disease*[tiab] OR “Lennox Gastaut Syndrome”[Mesh] OR lennox gastaut syndrome*[tiab]OR “Oculocerebrorenal Syndrome”[Mesh] OR lowe syndrome*[tiab] OR oculocerebrorenal syndrome*[tiab] OR Lowe Bickel Syndrome*[tiab] OR lowe diseas*[tiab] OR “Orofaciodigital Syndromes”[Mesh] OR orofaciodigital syndrome*[tiab] OR Dysplasia Linguofacialis[tiab] OR Gorlin Psaume Syndrome*[tiab] OR Mohr Syndrome*[tiab] OR “Ataxia Telangiectasia”[Mesh] OR ataxia telangiectas*[tiab] OR Louis Bar Syndrome*[tiab] OR “Pain Insensitivity, Congenital”[Mesh] OR Congenital Analgesia*[tiab] OR “Congenital Insensitivity To Pain”[tiab] OR Congenital Pain Indifference*[tiab] OR Congenital Pain Insensitivit*[tiab] OR “Congenital Indifference to Pain”[tiab] OR #(list ND/HPO for PubMed)NOT“Wolff-Parkinson-White Syndrome”[Mesh] OR “wolff-parkinson-white” OR WPW syndrome* OR “Fragile X Tremor Ataxia Syndrome”[Supplementary Concept] OR “Fragile X Tremor Ataxia” OR “FXTAS” OR “premutation” OR “Gaucher” OR “Gaucher Disease”[Mesh] OR Glucocerebrosidase deficienc* OR GBA deficienc* OR Wilson’s dis* OR Wilson dis* OR “Hepatolenticular Degeneration”[Mesh] OR “hepatolenticular Degeneration”EmbaseGeneral search termsParkinson/parkinsonism*Parkinson disease/ or *parkinsonism/ or Parkinson*.ti,ab,kw.AND