Generation of a human control iPSC line with a European mitochondrial haplogroup U background Fulltext Access 4 Pages 2016
Autoimmune autonomic ganglionopathy in a pediatric patient presenting with acute encephalitis Fulltext Access 4 Pages 2016
Usefulness of ketogenic diet in a girl with migrating partial seizures in infancy Fulltext Access 4 Pages 2016
Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation Fulltext Access 4 Pages 2016
A splicing mutation of proteolipid protein 1 in Pelizaeus-Merzbacher disease Fulltext Access 4 Pages 2016
Post-vaccination MDEM associated with MOG antibody in a subclinical Chlamydia infected boy Fulltext Access 4 Pages 2016
A girl with infantile neuronal ceroid lipofuscinosis caused by novel PPT1 mutation and paternal uniparental isodisomy of chromosome 1 Fulltext Access 4 Pages 2016
Diffusion restriction in ethylmalonic encephalopathy – An imaging evidence of the pathophysiology of the disease Fulltext Access 4 Pages 2016
Developmental changes in the hypothalamic mRNA levels of nucleobindin-2 (NUCB2) and their sensitivity to fasting in male and female rats Fulltext Access 4 Pages 2016
Prenatal undernutrition results in greater lipopolysaccharide-induced changes in hypothalamic TNF-α expression, but does not affect the equivalent changes in the serum levels of luteinizing hormone and testosterone, in adult male rats Fulltext Access 4 Pages 2016
Generation of a human iPSC line from a patient with a defect of intergenomic communication Fulltext Access 4 Pages 2016
Generation and characterization of human iPSC lines derived from a Primary Hyperoxaluria Type I patient with p.I244T mutation Fulltext Access 4 Pages 2016
Pathological crying and emotional vasovagal syncope as symptoms of a dorsally exophytic medullary tumor Fulltext Access 4 Pages 2016
Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT) Fulltext Access 4 Pages 2016
Human embryonic stem cells derived from abnormal blastocyst donated by glucose-6-phosphate dehydrogenase deficiency patient Fulltext Access 4 Pages 2016
Generation and characterization of human iPSC line generated from mesenchymal stem cells derived from adipose tissue Fulltext Access 4 Pages 2016
Transgene-free human induced pluripotent stem cell line (HS5-SV.hiPS) generated from cesarean scar-derived fibroblasts Fulltext Access 4 Pages 2016
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2A (MEN2A) syndrome with RET mutation Fulltext Access 4 Pages 2016
Generation of urine iPS cell line from a patient with obsessive-compulsive disorder using a non-integrative method Fulltext Access 4 Pages 2016
A human MIXL1 green fluorescent protein reporter embryonic stem cell line engineered using TALEN-based genome editing Fulltext Access 4 Pages 2016
Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a patient with recessive dystrophic epidermolysis bullosa (RDEB) carrying two compound heterozygous mutations in the COL7A1 gene Fulltext Access 4 Pages 2016
Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene Fulltext Access 4 Pages 2016
Generation of induced pluripotent stem cells (iPSCs) from a Bernard–Soulier syndrome patient carrying a W71R mutation in the GPIX gene Fulltext Access 4 Pages 2016
Management of Primary Headache in the Emergency Department and Inpatient Headache Unit Fulltext Access 4 Pages 2016
Trigeminal Autonomic Cephalalgias in Children and Adolescents: Cluster Headache and Related Conditions Fulltext Access 4 Pages 2016
Migrainous Aura, Visual Snow, and “Alice in Wonderland” Syndrome in Childhood Fulltext Access 4 Pages 2016
Frontal Aslant Tract Abnormality on Diffusion Tensor Imaging in an Aphasic Patient With 49, XXXXY Syndrome Fulltext Access 4 Pages 2016
Spinal Cord Stroke Presenting With Acute Monoplegia in a 17-Year-Old Tennis Player Fulltext Access 4 Pages 2016
Successful Treatment of Paroxysmal Movement Disorders of Infancy With Dimenhydrinate and Diphenhydramine Fulltext Access 4 Pages 2016
Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia Pigmenti Fulltext Access 4 Pages 2016
Oral Dimethyl Fumarate in Children With Multiple Sclerosis: A Dual-Center Study Fulltext Access 4 Pages 2016
Fatal Central Nervous System Disease Following First Infliximab Infusion in a Child With Inflammatory Bowel Disease Fulltext Access 4 Pages 2016
Hemifacial Spasm in a Child Treated With Microvascular Decompression of the Facial Nerve Fulltext Access 4 Pages 2016
Nutritional Status and Nutrient Intake Challenges in Children With Spinal Muscular Atrophy Fulltext Access 4 Pages 2016
Generation of a human iPSC line from a patient with an optic atrophy ‘plus’ phenotype due to a mutation in the OPA1 gene Fulltext Access 4 Pages 2016
Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome Fulltext Access 4 Pages 2016
Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation Fulltext Access 4 Pages 2016
A case of 3p deletion syndrome associated with cerebellar hemangioblastoma Fulltext Access 4 Pages 2016
Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency Fulltext Access 4 Pages 2016
Long-term weekly ACTH therapy for relapsed West syndrome in tuberous sclerosis complex: A case report Fulltext Access 4 Pages 2016
A case of anti-NMDAR encephalitis presented hypotensive shock during plasma exchange Fulltext Access 4 Pages 2016
Pre-school development and behavior screening with a consecutive support programs for 5-year-olds reduces the rate of school refusal Fulltext Access 4 Pages 2016
Relevance of endoglin, IL-1α, IL-1β and anti-ovarian antibodies in females with multiple sclerosis Fulltext Access 4 Pages 2016
Generation of KCL028 research grade human embryonic stem cell line carrying a mutation in the HTT gene Fulltext Access 4 Pages 2016
Generation of KCL027 research grade human embryonic stem cell line carrying a mutation in the HTT gene Fulltext Access 4 Pages 2016
Generation of KCL012 research grade human embryonic stem cell line carrying a mutation in the HTT gene Fulltext Access 4 Pages 2016
Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying an A79V mutation in PSEN1 Fulltext Access 4 Pages 2016
Derivation of human embryonic stem cell from spinal muscular atrophy patient Fulltext Access 4 Pages 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 gene Fulltext Access 4 Pages 2016
Generation of a gene-corrected isogenic control cell line from an Alzheimer's disease patient iPSC line carrying a A79V mutation in PSEN1 Fulltext Access 4 Pages 2016
Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 gene Fulltext Access 4 Pages 2016
Generation of induced pluripotent stem cells (iPSCs) from a retinoblastoma patient carrying a c.2663G > A mutation in RB1 gene Fulltext Access 4 Pages 2016
Gene promoter methylation and expression of Pin1 differ between patients with frontotemporal dementia and Alzheimer's disease Fulltext Access 4 Pages 2016
Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts Fulltext Access 4 Pages 2016
A suggested minimum standard deep brain stimulation evaluation for essential tremor Fulltext Access 4 Pages 2016
Increased 18F-FDG uptake in the trapezius muscle in patients with spinal accessory neuropathy Fulltext Access 4 Pages 2016
A novel hemizygous SACS mutation identified by whole exome sequencing and SNP array analysis in a Chinese ARSACS patient Fulltext Access 4 Pages 2016
Multiple sclerosis influences on the augmentation of serum Klotho concentration Fulltext Access 4 Pages 2016
Punding in non-demented Parkinson's disease patients: Relationship with psychiatric and addiction spectrum comorbidity Fulltext Access 4 Pages 2016
Relationship of circulatory BDNF with cognitive deficits in people with Parkinson's disease Fulltext Access 4 Pages 2016
Marked elevation of urinary β2-microglobulin in patients with reversible splenial lesions: A small case series Fulltext Access 4 Pages 2016
Predictive and prognostic value of TLR9 and NFKBIA gene expression as potential biomarkers for human glioma diagnosis Fulltext Access 4 Pages 2016
SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese Fulltext Access 4 Pages 2016
Transient global amnesia: Only in already disrupted neuronal integrity of memory network? Fulltext Access 4 Pages 2016
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11 Fulltext Access 4 Pages 2016
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11 Fulltext Access 4 Pages 2016
Derivation of Huntington Disease affected Genea017 human embryonic stem cell line Fulltext Access 4 Pages 2016
Heart rate variability to differentiate essential tremor from early-stage tremor-dominant Parkinson's disease Fulltext Access 4 Pages 2016
Derivation of Huntington disease affected Genea020 human embryonic stem cell line Fulltext Access 4 Pages 2016
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line Fulltext Access 4 Pages 2016
Derivation of Trisomy 21 affected human embryonic stem cell line Genea021 Fulltext Access 4 Pages 2016
Generation of KCL036 research grade human embryonic stem cell line carrying a mutation in the HTT gene Fulltext Access 4 Pages 2016
Generation of human control iPS cell line CHOPWT10 from healthy adult peripheral blood mononuclear cells Fulltext Access 4 Pages 2016
Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a M146I mutation in PSEN1 Fulltext Access 4 Pages 2016
Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using an integration free vector Fulltext Access 4 Pages 2016
Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2 Fulltext Access 4 Pages 2016