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Acute intermittent porphyria (AIP) (2)
Autoimmune-inflammatory diseases (2)
Brain (2)
Cineradiography (2)
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Deglutition disorders (2)
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Acquired immune deficiency syndrome (AIDS) (1)
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African ancestry (1)
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African trypanosomiasis -- Pretoria (South Africa) (1)
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Antero-medial globus pallidus internus (amGPi) (1)
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Attention deficit hyperactivity disorder (ADHD) (1)
Biophilic design (1)
Black African patients (1)
Bobble-head doll syndrome (BHDS) (1)
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Built environment (1)
CADASIL (1)
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Case studies (1)
Cerebral autosomal dominant arteriopathy (1)
Cerebrospinal fluid (CSF) JC virus (1)
Cerebrovascular disease -- Patients (1)
Childhood-onset generalised dystonia (1)
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Erythrocytes (RBCs) (1)
Facioscapulohumeral muscular dystrophy (1)
Familial adult myoclonic epilepsy (FAME) (1)
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Fibrin network (1)
Fibrin networks (1)
G2019S mutation (1)
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Glasgow coma scale (1)
Globus pallidus internus (GPi) (1)
Glucocerebrosidase (GBA) (1)
Guillain-Barré syndrome (1)
Guillain–Barré syndrome (1)
Haematopoietic stem cell transplantation (HSCT) (1)
Head bobbing (1)
Hemichorea-Athetose (1)
Henk w. mauser grading (1)
Hepatic porphyrias (1)
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HIV infections -- Complications -- South Africa (1)
HIV pandemic (1)
HIV-negative (1)
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HIV-positive persons -- South Africa (1)
HIV-related neurology patients (1)
HTLV-associated myelopathy (HAM) (1)
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Intracranial subdural empyema (1)
Isolated generalised dystonia (IGD) (1)
John Cunningham (JC) virus (1)
John Cunningham virus (1)
Ketotische Hyperglykämie (1)
Kyphosis (1)
Leucoencephalopathy (1)
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