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Ngoh, Adeline
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1

Molecular and Phenotypic Characterization of theRORB-Relate..:

Gokce-Samar, Zeynep ; Vetro, Annalisa ; De Bellescize, Julitta...
Neurology.  102 (2024)  2 - p. , 2024
Link: https://doi.org/10.1212/..
 
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2

Functional diversity of proline-substitution, epilepsy-asso..:

Gkotsi, Panagiota ; Miguel, Amaia Jauregi ; Pozzi, Serena...
Biophysical Journal.  123 (2024)  3 - p. 262a , 2024
Link: https://doi.org/10.1016/..
 
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3

Single-cell transcriptomics and surface epitope detection i..:

Kumar, Pavanish ; Lim, Amanda ; Hazirah, Sharifah Nur...
Nature Neuroscience.  25 (2022)  7 - p. 956-966 , 2022
Link: https://doi.org/10.1038/..
 
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4

Overview of Landau–Kleffner syndrome: early treatment, tail..:

Clark, Maria ; Holmes, Harriet ; Ngoh, Adeline..
Paediatrics and Child Health.  31 (2021)  5 - p. 207-219 , 2021
Link: https://doi.org/10.1016/..
 
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5

Unique Severe HyperEkplexia-Like Apneic Events (SHELAE) Imp..:

Krishnappa, Janardhan ; Ngoh, Adeline ; Hong, Yeo Tong..
Child Neurology Open.  8 (2021)  - p. 2329048X2110464 , 2021
Link: https://doi.org/10.1177/..
 
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6

KMT2B-related disorders: expansion of the phenotypic spectr..:

Cif, Laura ; Demailly, Diane ; Lin, Jean-Pierre...
Brain.  143 (2020)  11 - p. 3242-3261 , 2020
Link: https://doi.org/10.1093/..
 
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7

Proinflammatory IL-17 pathways dominate the architecture of..:

Kumar, Pavanish ; Shih, Derrick Chan Wei ; Lim, Amanda...
JCI Insight.  4 (2019)  8 - p. , 2019
Link: https://doi.org/10.1172/..
 
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8

Clinical and molecular characterization ofKCNT1-related sev..:

McTague, Amy ; Nair, Umesh ; Malhotra, Sony...
Neurology.  90 (2018)  1 - p. , 2018
Link: https://doi.org/10.1212/..
 
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9

TBC1D24 Mutations in a Sibship with MultifocalPolymyoclonus:

Ngoh, Adeline ; Bras, Jose ; Guerreiro, Rita...
Tremor and Other Hyperkinetic Movements.  7 (2017)  0 - p. 452 , 2017
Link: https://doi.org/10.5334/..
 
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10

New developments in epilepsy management:

Ngoh, Adeline ; Parker, Alasdair PJ
Paediatrics and Child Health.  27 (2017)  6 - p. 281-286 , 2017
Link: https://doi.org/10.1016/..
 
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11

Erratum: Corrigendum: Mutations in the histone methyltransf..:

UK10K Consortium ; Meyer, Esther ; Carss, Keren J...
Nature Genetics.  49 (2017)  6 - p. 969-969 , 2017
Link: https://doi.org/10.1038/..
 
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12

RARS2 mutations in a sibship with infantile spasms:

Ngoh, Adeline ; Bras, Jose ; Guerreiro, Rita...
Epilepsia.  57 (2016)  5 - p. , 2016
Link: https://doi.org/10.1111/..
 
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13

Delineation of the movement disorders associated withFOXG1m..:

Papandreou, Apostolos ; Schneider, Ruth B. ; Augustine, Erika F....
Neurology.  86 (2016)  19 - p. 1794-1800 , 2016
Link: https://doi.org/10.1212/..
 
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14

Mutations in the histone methyltransferase gene KMT2B cause..:

UK10K Consortium ; Meyer, Esther ; Carss, Keren J...
Nature Genetics.  49 (2016)  2 - p. 223-237 , 2016
Link: https://doi.org/10.1038/..
 
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15

GABRB3 mutations: a new and emerging cause of early infanti..:

Papandreou, Apostolos ; McTague, Amy ; Trump, Natalie...
Developmental Medicine & Child Neurology.  58 (2015)  4 - p. 416-420 , 2015
Link: https://doi.org/10.1111/..
 
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