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                             41 results found
no title author magazine year volume issue page(s) type
1 A Boy With Red Ears Coleman, Juliana
 2018
 26 C p. 92-93
 article
2 A Case of An Unusual Bell’s Palsy Mimic Lutley, Alexandria L.
 2018
 26 C p. 77-79
 article
3 A 15-Month-Old Girl Presenting With Clitoromegaly and a Chest Mass Darcy, Courtney
 2018
 26 C p. 128-131
 article
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
 article
5 A Newborn With Hyperlactatemia and Epileptic Encephalopathy Obeid, Rawad
 2018
 26 C p. 104-107
 article
6 A Novel Phenotype in a Previously Described Epilepsy—Aphasia Disorder Fine, Anthony L.
 2018
 26 C p. 21-24
 article
7 A Quiet Disease With Loud Manifestations Moresco, Benjamin Louis
 2018
 26 C p. 88-91
 article
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
 article
9 A 2-Year-Old Boy With Difficulty Waking After Bone Marrow Transplantation Broomall, Eileen
 2018
 26 C p. 120-123
 article
10 A 15-Year-Old Boy With Refractory Status Epilepticus Shukla, Nikita Malani
 2018
 26 C p. 101-103
 article
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
 article
12 “Cerebral Palsy” in a Patient With Arginase Deficiency Jichlinski, Amanda
 2018
 26 C p. 110-114
 article
13 Consideration of Genetic Diagnoses of Developmental Delay in Children of Consanguineous Families Sadeghi, Salva
 2018
 26 C p. 60-62
 article
14 Diplopia With Dural Fibrotic Thickening Brand, Brittany
 2018
 26 C p. 83-87
 article
15 Editorial: A Terrible Time Bodensteiner, John B.
 2018
 26 C p. 45
 article
16 Editorial Comment: Brown-Vialetto-Van Laere and the Advances in Molecular Medicine Bodensteiner, John B.
 2018
 26 C p. 15
 article
17 Editorial Comment Case #14 Basilar Artery Thrombosis in a Neonate Bodensteiner, John B.
 2018
 26 C p. 67
 article
18 Editorial Comment: Case #26 Hypothalamic Hamartoma and Infantile Spasms Bodensteiner, John B.
 2018
 26 C p. 119
 article
19 Editorial Comment: Cases #27-31 Bodensteiner, John B.
 2018
 26 C p. 140
 article
20 Editorial to Follow Case #21 Regarding Cases #14-21 Bodensteiner, John B.
 2018
 26 C p. 94
 article
21 Editorial (To Follow Cases #9-12) Bodensteiner, John B.
 2018
 26 C p. 59
 article
22 Elevated Creatine Kinase in a 6-Year-Old Boy Chan, Eunice K.
 2018
 26 C p. 46-49
 article
23 Facial Weakness and Ophthalmoplegia in a 4-Day-Old Infant Kouri, Ioanna
 2018
 26 C p. 63-66
 article
24 Focal Epilepsy in a Teenager With Facial Atrophy and Hair Loss English, Stephen W.
 2018
 26 C p. 68-73
 article
25 Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome Woodcock, Ian R.
 2018
 26 C p. 2-9
 article
26 Hypothalamic Hamartoma With Infantile Spasms: Case Report With Surgical Treatment Fox, Jordana
 2018
 26 C p. 115-118
 article
27 Infantile Epileptic Encephalopathy With Multiple Genetic Mutations: How Important are Variants of Undetermined Significance? Almomen, Momen
 2018
 26 C p. 33-36
 article
28 Infantile-Onset Myelin Protein Zero–Related Demyelinating Neuropathy Presenting as an Upper Extremity Monoplegia Yiu, Eppie M.
 2018
 26 C p. 52-55
 article
29 Intracranial Calcifications in Young Children Dugan, Sarah L.
 2018
 26 C p. 135-139
 article
30 Introduction to the Issue Bodensteiner, John B.
 2018
 26 C p. 1
 article
31 Language Regression in an Atypical SLC6A1 Mutation Islam, Monica P.
 2018
 26 C p. 25-27
 article
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
 article
33 Multifocal Brain Lesions With Extensive Perilesional Edema in a Young Boy Returning From Kenya Merison, Kelsey
 2018
 26 C p. 132-134
 article
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
 article
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
 article
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
 article
37 Status Epilepticus—The Hunt for Treatable Causes Payne, Eric T.
 2018
 26 C p. 108-109
 article
38 The Curse of Apneic Spells Radke, Josefine
 2018
 26 C p. 56-58
 article
39 The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa Chaya, Shaakira
 2018
 26 C p. 10-14
 article
40 The More Things Change… Child Neurology in the Age of Next-Generation Sequencing Patterson, Marc C.
 2018
 26 C p. 37-38
 article
41 The Terrible Summer of 1952 … When Polio Struck Our Family Strand, Linda Knutson
 2018
 26 C p. 39-44
 article
                             41 results found
 
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