| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ante- and Perinatal Factors for Cerebral Palsy: Case-Control Study in Estonia
|
Stelmach, Tiina
|
|
2005
|
20 |
8 |
p. 654-661
|
artikel
|
| 2 |
Certification in Child Neurology: New Directions for the Twenty-First Century
|
Percy, K.
|
|
2005
|
20 |
8 |
p. 644-647
|
artikel
|
| 3 |
Comorbidity of Epilepsy and Headache in Patients With Sturge-Weber Syndrome
|
Hatfield, Laura A.
|
|
2005
|
20 |
8 |
p. 678-682
|
artikel
|
| 4 |
Developmental and Functional Outcomes at School Age of Preschool Children With Global Developmental Delay
|
Shevell, Michael
|
|
2005
|
20 |
8 |
p. 648-654
|
artikel
|
| 5 |
Dissecting MECP2 Function in the Central Nervous System
|
Kishi, Noriyuki
|
|
2005
|
20 |
8 |
p. 753-759
|
artikel
|
| 6 |
Does Genotype Predict Phenotype in Rett Syndrome?
|
Ham, Andrea L.
|
|
2005
|
20 |
8 |
p. 768-778
|
artikel
|
| 7 |
Efficacy and Tolerability of Topiramate in Children Younger Than 2 Years Old
|
Valencia, Ignacio
|
|
2005
|
20 |
8 |
p. 667-670
|
artikel
|
| 8 |
Embryology of the Neural Crest: Its Inductive Role in the Neurocutaneous Syndromes
|
Sarnat, Harvey B.
|
|
2005
|
20 |
8 |
p. 637-643
|
artikel
|
| 9 |
Factors Predicting the Efficacy of Botulinum Toxin-A Treatment of the Lower Limb in Children With Cerebral Palsy
|
Fazzi, Elisa
|
|
2005
|
20 |
8 |
p. 661-666
|
artikel
|
| 10 |
Focal Status Epilepticus as Atypical Presentation of Pyridoxine-Dependent Epilepsy
|
Yoshii, Akira
|
|
2005
|
20 |
8 |
p. 696-698
|
artikel
|
| 11 |
Hallermann-Streiff Syndrome Associated With Complete Agenesis of the Corpus Callosum
|
Siğirci, Ahmet
|
|
2005
|
20 |
8 |
p. 691-693
|
artikel
|
| 12 |
Intrapartum Complications Associated With Malformations of Cortical Development
|
Montenegro, Maria Augusta
|
|
2005
|
20 |
8 |
p. 675-678
|
artikel
|
| 13 |
MECP2 Abnormality Phenotypes: Clinicopathologic Area With Broad Variability
|
Erlandson, Anna
|
|
2005
|
20 |
8 |
p. 727-732
|
artikel
|
| 14 |
MeCP2 Dysfunction in Humans and Mice
|
Zoghbi, Huda Y.
|
|
2005
|
20 |
8 |
p. 736-740
|
artikel
|
| 15 |
Molecular Diagnosis of Rett Syndrome
|
Huppke, Peter
|
|
2005
|
20 |
8 |
p. 732-736
|
artikel
|
| 16 |
Multivoxel Magnetic Resonance Spectroscopy in a Rhizomelic Chondrodysplasia Punctata Case
|
Siğirci, Ahmet
|
|
2005
|
20 |
8 |
p. 698-701
|
artikel
|
| 17 |
Natural History of Rett Syndrome
|
Nomura, Yoshiko
|
|
2005
|
20 |
8 |
p. 764-768
|
artikel
|
| 18 |
Neuropathology of Rett Syndrome
|
Armstrong, Dawna Duncan
|
|
2005
|
20 |
8 |
p. 747-753
|
artikel
|
| 19 |
Neurophysiology of Rett Syndrome
|
Glaze, Daniel G.
|
|
2005
|
20 |
8 |
p. 740-746
|
artikel
|
| 20 |
Newborn Screening and Prenatal Diagnosis for Rett Syndrome: Implications for Therapy
|
Amir, Ruthie E.
|
|
2005
|
20 |
8 |
p. 779-783
|
artikel
|
| 21 |
Nonconvulsive Status Epilepticus Precipitated by Carbamazepine Presenting as Dissociative and Affective Disorders in Adolescents
|
Marini, Carla
|
|
2005
|
20 |
8 |
p. 693-696
|
artikel
|
| 22 |
Relationship Between Brain Glucose Metabolism Positron Emission Tomography (PET) and Electroencephalography (EEG) in Children With Continuous Spike-and-Wave Activity During Slow-Wave Sleep
|
Luat, Aimee F.
|
|
2005
|
20 |
8 |
p. 682-690
|
artikel
|
| 23 |
Rett Syndrome
|
Maria, Bernard L.
|
|
2005
|
20 |
8 |
p. 707-707
|
artikel
|
| 24 |
Rett Syndrome and Neuronal Development
|
Johnston, Michael V.
|
|
2005
|
20 |
8 |
p. 759-763
|
artikel
|
| 25 |
Rett Syndrome: Long-Term Clinical Follow-Up Experiences Over Four Decades
|
Hagberg, Bengt
|
|
2005
|
20 |
8 |
p. 722-727
|
artikel
|
| 26 |
Rett Syndrome: Model of Neurodevelopmental Disorders
|
Percy, Alan K.
|
|
2005
|
20 |
8 |
p. 718-721
|
artikel
|
| 27 |
Rett Syndrome: Pathogenesis, Diagnosis, Strategies, Therapies, and Future Research Directions
|
Deidrick, Kathleen M.
|
|
2005
|
20 |
8 |
p. 708-717
|
artikel
|
| 28 |
The Human Secretin Gene in Children With Autistic Spectrum Disorder: Screening for Polymorphisms and Mutations
|
Ng, Samuel S.M.
|
|
2005
|
20 |
8 |
p. 701-704
|
artikel
|
| 29 |
Unusual Clinical Presentations in Four Cases of Leigh Disease, Cytochrome C Oxidase Deficiency, and SURF1 Gene Mutations
|
Tay, Stacey K.H.
|
|
2005
|
20 |
8 |
p. 670-674
|
artikel
|
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