1,095 results on '"Myers, Kenneth A."'
Search Results
52. Cation leak: a common functional defect causing HCN1 developmental and epileptic encephalopathy
53. Teaching NeuroImages: MRI findings in X-linked adrenoleukodystrophy
54. Teaching NeuroImage: Low-Frequency Photoparoxysmal Response in a Patient With Neuronal Ceroid Lipofuscinosis Type 2
55. Sclerotherapy of lower limb veins: Indications, contraindications and treatment strategies to prevent complications – A consensus document of the International Union of Phlebology-2023
56. WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
57. "It Becomes a Family I'm a Part of...We Get to Carry Each Other": Themes from Qualitative Interview of Patients Enrolled in an Inpatient Palliative Care Support Program for Adolescents and Young Adults.
58. Digital Insanity: Exploring the Flexibility of NIST Digital Identity Assurance Levels
59. Clinton creek abandoned mine/interim spillway reclamation project—status of the channel restoration effort
60. Comparison between endothelial and tumor cells in the response to verteporfin-photodynamic therapy and a PI3K pathway inhibitor
61. Response to Hydrocortisone in an Extremely Preterm Neonate With Late-Onset Sepsis, Meningoencephalitis, and Drug-Resistant Seizures
62. Not a Benign Vitamin: Infant with Vitamin A Toxicity and Acute Intracranial Hypertension
63. A Novel Palliative Care Peer Support Program for Adolescents and Young Adults: Survey and Factor Analytic Study
64. “Generalized‐to‐focal” epilepsy: stereotactic EEG and high‐frequency oscillation patterns
65. Cerebral Edema in Maple Syrup Urine Disease Despite Newborn Screening Diagnosis and Early Initiation of Treatment
66. Microtubule–Actin Interactions During Neuronal Development
67. Randomized placebo-controlled crossover trial of memantine in children with epileptic encephalopathy
68. Homozygous THAP1 pathogenic variant causes early onset multifocal dystonia with severe oromandibular/laryngeal dysfunction
69. Surgically Remediable Secondary Network Epileptic Encephalopathies With Continuous Spike Wave in Sleep: Lesions May Not Be Visible on Brain Magnetic Resonance Imaging (MRI)
70. Post-vaccination drug-resistant epileptic spasms associated with homozygous IFNAR2 pathogenic variant: Case report✰
71. Koolen‐de Vries syndrome associated with continuous spike‐wave in sleep
72. Actin capping protein regulates postsynaptic spine development through CPI-motif interactions
73. Electrically detected electron nuclear double resonance in amorphous hydrogenated boron thin films
74. Cerebral white matter abnormalities associated with chromosome 18q duplication
75. ADGRV1 is implicated in myoclonic epilepsy
76. Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay
77. Ataxia and Diplopia: A New SCN8A-Related Phenotype.
78. MT‐TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy
79. One pot, two step sequence converting atom transfer radical polymerization directly to radical trap-assisted atom transfer radical coupling
80. Blakeʼs pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes
81. De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome
82. A Novel Palliative Care Peer Support Program for Adolescents and Young Adults: Survey and Factor Analytic Study.
83. Randomized placebo-controlled crossover trial of memantine in children with epileptic encephalopathy.
84. Septins guide noncentrosomal microtubules to promote focal adhesion disassembly in migrating cells
85. The spectrum of indomethacin-responsive headaches in children and adolescents
86. De novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations without Skeletal Abnormalities
87. Whistler the "Quintessencier: Violet and Blue: Among the Rollers" and the Importance of the Late Small Oils
88. sj-docx-1-cno-10.1177_2329048X221093173 - Supplemental material for Genetic Generalized Epilepsy and Intrafamilial Phenotypic Variability with Distal 7q11.23 Deletion
89. Reinventing the American Wing : The Detroit Institute of Arts
90. A Neuron-Specific Cytoplasmic Dynein Isoform Preferentially Transports TrkB Signaling Endosomes
91. Clinical assessment of diseases of lower limb arteries
92. Is There a Place for Instructional Design in the Information Age?
93. Kinesin-5 Regulates the Growth of the Axon by Acting as a Brake on Its Microtubule Array
94. Precision Medicine Approaches for Infantile-Onset Developmental and Epileptic Encephalopathies
95. SUDEP risk and autonomic dysfunction in genetic epilepsies
96. Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome
97. New interinstitutional, multimodal presurgical evaluation protocol associated with improved seizure freedom for poorly defined cases of focal epilepsy in children
98. Genetic Generalized Epilepsy and Intrafamilial Phenotypic Variability with Distal 7q11.23 Deletion
99. FACTS FOR PROSPECTIVE FARMERS.
100. "Type of a Back Civilization": Worthington Whittredge's Santa Fe
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.