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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abnormal Genetic Testing in Males With Concomitant Neurodevelopmental Disabilities and Genital Malformation Pham, Tri

134 C p. 72-77
artikel
2 Association Between Early EEG Background and Outcomes in Infants With Mild HIE Undergoing Therapeutic Hypothermia Natarajan, Niranjana

134 C p. 52-58
artikel
3 Association of EEG and Blood-Based Brain Injury Biomarker Accuracy to Prognosticate Mortality After Pediatric Cardiac Arrest: An Exploratory Study Anetakis, Katherine M.

134 C p. 25-30
artikel
4 A Systematic Review of Recent and Ongoing Clinical Trials in Patients With the Neurofibromatoses Acar, Simge

134 C p. 1-6
artikel
5 Cerebral Arterial Growth in Childhood Taylor, J. Michael

134 C p. 59-66
artikel
6 Cerebrovascular Complications of COVID-19 Disease in Children: A Single-Center Case Series Španělová, Klára

134 C p. 18-24
artikel
7 Characteristics of Moyamoya Syndrome in Pediatric Patients With Neurofibromatosis Type 1 Brosius, Stephanie N.

134 C p. 85-92
artikel
8 Comparison of Clinical Manifestations, Laboratory, Neuroimaging Findings, and Outcomes in Children With Posterior Reversible Encephalopathy Syndrome (PRES) in Children With and Without Renal Disease Virojtriratana, Tananat

134 C p. 37-44
artikel
9 Comparison of Impairment in Functional Tic Disorders Versus Tourette Syndrome Larsh, Travis R.

134 C p. 83-84
artikel
10 Early Spontaneous Movements and Upper Extremity Movement Score in Infants With all Narakas Types of Obstetric Brachial Plexus Palsy Yardımcı-Lokmanoğlu, Bilge Nur

134 C p. 11-17
artikel
11 Editorial Board and Masthead
134 C p. A1-A2
artikel
12 Hereditary Hyperekplexia in Saudi Arabia Aldhilan, Amal

134 C p. 78-82
artikel
13 HLA-DRB1∗1502 Is Associated With Anti-N-Methyl-D-aspartate Receptor Encephalitis in Thai Children Anurat, Kingthong

134 C p. 93-99
artikel
14 Hypogammaglobulinemia Associated With Oxcarbazepine Use in a Teen Toohey, Caitlin V.

134 C p. 67-70
artikel
15 Infantile-Onset Complex Hereditary Spastic Paraplegia Due to a Novel Mutation in SPAST Gene ElSheikh, Reem H.

134 C p. 71
artikel
16 MECP2 Dysautonomia Phenotypes in Boys Courgeon, Lisa

134 C p. 31-36
artikel
17 Table of Contents
134 C p. A3-A4
artikel
18 The Outcome of COVID-19 in Pediatric-Onset Multiple Sclerosis Patients Oncel, Ibrahim

134 C p. 7-10
artikel
19 Use of Magnetic Resonance Imaging in Neuroprognostication After Pediatric Cardiac Arrest: Survey of Current Practices Piantino, Juan A.

134 C p. 45-51
artikel
                             19 gevonden resultaten
 
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