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PubPharm (469)
31
'Advocacy groups are the connectors' : Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics
enthalten in:
Health expectations : an international journal of public participation in health care and health policy
| 2022
von
Nguyen, C.
|
Kariyawasam, D.
|
Alba-Concepcion, K.
| +7
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32
Association of maternal autoimmune disease and early childhood infections with offspring autism spectrum disorder : A population-based cohort study
enthalten in:
Autism research : official journal of the International Society for Autism Research
| 2022
von
Nielsen, T.
|
Nassar, N.
|
Shand, A.
| +6
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33
Insights into the genetic architecture underlying complex, critical congenital heart disease
enthalten in:
American heart journal
| 2022
von
Blue, G.
|
Ip, E.
|
Troup, M.
| +6
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34
Steroid-responsive aseptic meningitis with raised intracranial pressure syndrome associated with myelin oligodendrocyte glycoprotein autoantibodies
enthalten in:
Journal of paediatrics and child health
| 2022
von
Wong, W.
|
Troedson, C.
|
Peacock, K.
| +4
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35
Persistent Inflammation in Cerebral Palsy : Pathogenic Mediator or Comorbidity? A Scoping Review
enthalten in:
Journal of clinical medicine
| 2022
von
Paton, M.
|
Finch-Edmondson, M.
|
Dale, R.
| +5
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36
Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy
enthalten in:
Human mutation
| 2022
von
Rius, R.
|
Bennett, N.
|
Bhattacharya, K.
| +13
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37
COVID-19 Vaccination in Young People with Functional Neurological Disorder : A Case-Control Study
enthalten in:
Vaccines
| 2022
von
Lim, N.
|
Wood, N.
|
Prasad, A.
| +6
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38
The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Pérez-Dueñas, B.
|
Gorman, K.
|
Marcé-Grau, A.
| +23
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39
Decreased cerebrospinal fluid kynurenic acid in epileptic spasms : A biomarker of response to corticosteroids
enthalten in:
EBioMedicine
| 2022
von
Yan, J.
|
Kothur, K.
|
Innes, E.
| +20
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40
Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in AFG3L2
enthalten in:
Movement disorders clinical practice
| 2022
von
Wong, W.
|
Troedson, C.
|
Dale, R.
| +6
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Developmental medicine and child neurology
27
Developmental medicine & child neurology
22
Neurology
16
Movement disorders : official journal of the Mo...
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Developmental Medicine & Child Neurology
12
Neurology(R) neuroimmunology & neuroinflammation
11
Journal of paediatrics and child health
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Movement disorders
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Pediatric neurology
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Annals of neurology
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Epilepsia
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European journal of paediatric neurology : EJPN...
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Journal of neurology, neurosurgery, and psychiatry
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Multiple sclerosis (Houndmills, Basingstoke, En...
7
Journal of neuroimmunology
6
Journal of child neurology
6
Movement Disorders
6
Nature genetics
5
Brain : a journal of neurology
5
Current opinion in neurology
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Thema
264
Journal Article
134
Research Support, Non-U.S. Gov't
62
Autoantibodies
57
Review
51
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23
Biomarkers
23
Myelin-Oligodendrocyte Glycoprotein
20
Comment
19
Research Support, N.I.H., Extramural
17
Letter
16
Encephalitis
16
Immunoglobulin G
14
Systematic Review
13
Editorial
13
Receptors, N-Methyl-D-Aspartate
12
Antibodies
12
Nerve Tissue Proteins
11
Multicenter Study
10
Autoantigens
10
Membrane Proteins
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