| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Boy With Red Ears
|
Coleman, Juliana
|
|
2018
|
26 |
C |
p. 92-93
|
artikel
|
| 2 |
A Case of An Unusual Bell’s Palsy Mimic
|
Lutley, Alexandria L.
|
|
2018
|
26 |
C |
p. 77-79
|
artikel
|
| 3 |
A 15-Month-Old Girl Presenting With Clitoromegaly and a Chest Mass
|
Darcy, Courtney
|
|
2018
|
26 |
C |
p. 128-131
|
artikel
|
| 4 |
A 20-Month-Old Girl With Fever, Seizures, Hemiparesis, and Brain Lesions Requiring a Diagnostic Brain Biopsy
|
Matsumoto, Satsuki
|
|
2018
|
26 |
C |
p. 80-82
|
artikel
|
| 5 |
A Newborn With Hyperlactatemia and Epileptic Encephalopathy
|
Obeid, Rawad
|
|
2018
|
26 |
C |
p. 104-107
|
artikel
|
| 6 |
A Novel Phenotype in a Previously Described Epilepsy—Aphasia Disorder
|
Fine, Anthony L.
|
|
2018
|
26 |
C |
p. 21-24
|
artikel
|
| 7 |
A Quiet Disease With Loud Manifestations
|
Moresco, Benjamin Louis
|
|
2018
|
26 |
C |
p. 88-91
|
artikel
|
| 8 |
Atypical Presentation of a Progressive and Treatable Encephalopathy in an Older Child With Gelastic and Dacrystic Seizures
|
Vidaurre, Jorge
|
|
2018
|
26 |
C |
p. 95-100
|
artikel
|
| 9 |
A 2-Year-Old Boy With Difficulty Waking After Bone Marrow Transplantation
|
Broomall, Eileen
|
|
2018
|
26 |
C |
p. 120-123
|
artikel
|
| 10 |
A 15-Year-Old Boy With Refractory Status Epilepticus
|
Shukla, Nikita Malani
|
|
2018
|
26 |
C |
p. 101-103
|
artikel
|
| 11 |
A 15-Year-Old Girl With Sudden Onsent Reversible Neurologic Symptoms After Cranial Irradiation for Medulloblastoma
|
Duke, Elizabeth
|
|
2018
|
26 |
C |
p. 124-127
|
artikel
|
| 12 |
“Cerebral Palsy” in a Patient With Arginase Deficiency
|
Jichlinski, Amanda
|
|
2018
|
26 |
C |
p. 110-114
|
artikel
|
| 13 |
Consideration of Genetic Diagnoses of Developmental Delay in Children of Consanguineous Families
|
Sadeghi, Salva
|
|
2018
|
26 |
C |
p. 60-62
|
artikel
|
| 14 |
Diplopia With Dural Fibrotic Thickening
|
Brand, Brittany
|
|
2018
|
26 |
C |
p. 83-87
|
artikel
|
| 15 |
Editorial: A Terrible Time
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 45
|
artikel
|
| 16 |
Editorial Comment: Brown-Vialetto-Van Laere and the Advances in Molecular Medicine
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 15
|
artikel
|
| 17 |
Editorial Comment Case #14 Basilar Artery Thrombosis in a Neonate
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 67
|
artikel
|
| 18 |
Editorial Comment: Case #26 Hypothalamic Hamartoma and Infantile Spasms
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 119
|
artikel
|
| 19 |
Editorial Comment: Cases #27-31
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 140
|
artikel
|
| 20 |
Editorial to Follow Case #21 Regarding Cases #14-21
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 94
|
artikel
|
| 21 |
Editorial (To Follow Cases #9-12)
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 59
|
artikel
|
| 22 |
Elevated Creatine Kinase in a 6-Year-Old Boy
|
Chan, Eunice K.
|
|
2018
|
26 |
C |
p. 46-49
|
artikel
|
| 23 |
Facial Weakness and Ophthalmoplegia in a 4-Day-Old Infant
|
Kouri, Ioanna
|
|
2018
|
26 |
C |
p. 63-66
|
artikel
|
| 24 |
Focal Epilepsy in a Teenager With Facial Atrophy and Hair Loss
|
English, Stephen W.
|
|
2018
|
26 |
C |
p. 68-73
|
artikel
|
| 25 |
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome
|
Woodcock, Ian R.
|
|
2018
|
26 |
C |
p. 2-9
|
artikel
|
| 26 |
Hypothalamic Hamartoma With Infantile Spasms: Case Report With Surgical Treatment
|
Fox, Jordana
|
|
2018
|
26 |
C |
p. 115-118
|
artikel
|
| 27 |
Infantile Epileptic Encephalopathy With Multiple Genetic Mutations: How Important are Variants of Undetermined Significance?
|
Almomen, Momen
|
|
2018
|
26 |
C |
p. 33-36
|
artikel
|
| 28 |
Infantile-Onset Myelin Protein Zero–Related Demyelinating Neuropathy Presenting as an Upper Extremity Monoplegia
|
Yiu, Eppie M.
|
|
2018
|
26 |
C |
p. 52-55
|
artikel
|
| 29 |
Intracranial Calcifications in Young Children
|
Dugan, Sarah L.
|
|
2018
|
26 |
C |
p. 135-139
|
artikel
|
| 30 |
Introduction to the Issue
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 1
|
artikel
|
| 31 |
Language Regression in an Atypical SLC6A1 Mutation
|
Islam, Monica P.
|
|
2018
|
26 |
C |
p. 25-27
|
artikel
|
| 32 |
McArdle Disease Presenting With Muscle Pain in a Teenage Girl: The Role of Whole-Exome Sequencing in Neurogenetic Disorders
|
Walters, William D.
|
|
2018
|
26 |
C |
p. 50-51
|
artikel
|
| 33 |
Multifocal Brain Lesions With Extensive Perilesional Edema in a Young Boy Returning From Kenya
|
Merison, Kelsey
|
|
2018
|
26 |
C |
p. 132-134
|
artikel
|
| 34 |
Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results
|
Gerald, Brittany
|
|
2018
|
26 |
C |
p. 28-32
|
artikel
|
| 35 |
Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype
|
Conboy, Erin
|
|
2018
|
26 |
C |
p. 16-20
|
artikel
|
| 36 |
Pseudobulbar Affect in Survivors of Extreme Prematurity With Cerebellar Injury: Support for the Cerebellar Link in Pathologic Laughter and Crying
|
Bodensteiner, John B.
|
|
2018
|
26 |
C |
p. 74-76
|
artikel
|
| 37 |
Status Epilepticus—The Hunt for Treatable Causes
|
Payne, Eric T.
|
|
2018
|
26 |
C |
p. 108-109
|
artikel
|
| 38 |
The Curse of Apneic Spells
|
Radke, Josefine
|
|
2018
|
26 |
C |
p. 56-58
|
artikel
|
| 39 |
The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa
|
Chaya, Shaakira
|
|
2018
|
26 |
C |
p. 10-14
|
artikel
|
| 40 |
The More Things Change… Child Neurology in the Age of Next-Generation Sequencing
|
Patterson, Marc C.
|
|
2018
|
26 |
C |
p. 37-38
|
artikel
|
| 41 |
The Terrible Summer of 1952 … When Polio Struck Our Family
|
Strand, Linda Knutson
|
|
2018
|
26 |
C |
p. 39-44
|
artikel
|
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