Page 61 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma

Parkinsonism in GNDs
Alagille*[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”
Embase
General search terms
Parkinson/parkinsonism
*Parkinson disease/ or *parkinsonism/ or Parkinson*.ti,ab,kw.
AND
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