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                             23 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of spinal muscular atrophy type 0 treated with nusinersen without progression of early-onset scoliosis – possibility of preventing scoliosis with a rehabilitation program focusing on postural management Kimizu, Tomokazu

47 3 p.
artikel
2 A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literature Politano, Davide

47 3 p.
artikel
3 Age-related variations in opening pressure in lumbar puncture: Implications for its interpretation in children Farfán-Albarracín, Juan David

47 3 p.
artikel
4 Autism-like features and FOXP1 syndrome: A scoping review Stewart, Jayme

47 3 p.
artikel
5 Brain dysfunction underlying visual snow syndrome: Insights into therapeutic implications Shibata, Mamoru

47 3 p.
artikel
6 Brown-Vialetto-Van Laere syndrome patients with unusual phenotypes from Indian ethnicity: Functional analysis of clinical variants in SLC52A2 and SLC52A3 genes Gayathri, Santhalingam

47 3 p.
artikel
7 Can a familial history of migraine and motion sickness be used in the diagnosis of childhood migraine? Cokyaman, Turgay

47 3 p.
artikel
8 Challenges in genetic counseling for RYR1-related myopathies Shimomura, Rina

47 3 p.
artikel
9 Characteristics of neonatal-onset and presumed neonatal arterial ischemic stroke Ueda, Kazuto

47 3 p.
artikel
10 Clinical characteristics and radiological features of tubulinopathy: A single-center retrospective study in Japan Ikegawa, Tamaki

47 3 p.
artikel
11 COVID-19 infection and vaccination in children with Dravet syndrome or infantile epileptic spasms syndrome: An internet survey in Japan Ito, Susumu

47 3 p.
artikel
12 Development of a manual for an upper extremity intensive rehabilitation program for pediatric hemiplegia in Japan and assessment of its effectiveness and usability Katori, Sayaka

47 3 p.
artikel
13 Diagnostic value of serum miRNA-134-3p and miRNA-155-5p for monitoring seizure control in pediatric epilepsy Yang, Yating

47 3 p.
artikel
14 Diffuse but Non-homogeneous Brain Atrophy: Identification of Specific Brain Regions and Their Correlation with Clinical Severity in Rett Syndrome Narita, Hajime

47 3 p.
artikel
15 Influence of SARS-CoV-2 omicron variant infection on seizure occurrence among children: The large-scale multicenter study Kong, Juhyun

47 3 p.
artikel
16 Intellectual disability and genotype-phenotype correlation between full-scale intelligence quotient and mutation characteristics in boys with dystrophinopathy Sharawat, Indar Kumar

47 3 p.
artikel
17 Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide survey Okazaki, Tetsuya

47 3 p.
artikel
18 JSCN Best Paper Awards
47 3 p.
artikel
19 Magnetic resonance imaging and spectroscopy in hypomyelinating leukodystrophy Takanashi, Jun-ichi

47 3 p.
artikel
20 Risk factors for sedation and MRI failure in children with neurodevelopmental disorders undergoing head MRI with oral triclofos sodium and/or rectal chloral hydrate Zensho, Kazumasa

47 3 p.
artikel
21 Synaptic disturbance in neurodevelopmental disorders: Perspectives from fragile X and Rett syndromes Li, Ruixiang

47 3 p.
artikel
22 Tryptophan metabolism in children with migraine: The role of kynurenine pathway Şahin, Şeyma Sönmez

47 3 p.
artikel
23 Volumetric and microstructural changes in the Hippocampus and cingulum in children with west syndrome PALANCI, Özgür

47 3 p.
artikel
                             23 gevonden resultaten
 
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