Cargando…

GLUT1 deficiency: Retinal detrimental effects of gliovascular modulation

Detalles Bibliográficos
Autores principales:	Henry, Matt, Kitchens, John, Pascual, Juan M., Maldonado, Ramiro S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2020
Materias:	Clinical/Scientific Notes
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413606/ https://www.ncbi.nlm.nih.gov/pubmed/32802945 http://dx.doi.org/10.1212/NXG.0000000000000472

Ejemplares similares

Gliovascular and cytokine interactions modulate brain endothelial barrier in vitro
por: Chaitanya, Ganta V, et al.
Publicado: (2011)

Evaluation of gliovascular functions of Aqp4 readthrough isoforms
por: Mueller, Shayna M., et al.
Publicado: (2023)

Contribution of blood vessels to retinal nerve fiber layer thickness in NMOSD
por: Oertel, Frederike C., et al.
Publicado: (2017)

Toll-like receptor 3 deficiency in autoimmune encephalitis post–herpes simplex encephalitis
por: Armangue, Thaís, et al.
Publicado: (2019)

VZV-associated acute retinal necrosis in a patient with MS treated with natalizumab
por: Pawlitzki, Marc, et al.
Publicado: (2018)

Hyperventilation-athetosis in ASXL3 deficiency (Bainbridge-Ropers) syndrome
por: Dad, Rubina, et al.
Publicado: (2017)

Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface
por: Boulay, Anne- Cécile, et al.
Publicado: (2017)

Seizures elevate gliovascular unit Ca(2+) and cause sustained vasoconstriction
por: Tran, Cam Ha T., et al.
Publicado: (2020)

Obesity-associated hyperleptinemia alters the gliovascular interface of the hypothalamus to promote hypertension
por: Gruber, Tim, et al.
Publicado: (2021)

Megalencephalic leukoencephalopathy with subcortical cysts is a developmental disorder of the gliovascular unit
por: Gilbert, Alice, et al.
Publicado: (2021)

Transcriptomic Profiling Reveals Discrete Poststroke Dementia Neuronal and Gliovascular Signatures
por: Waller, Rachel, et al.
Publicado: (2022)

Leaky splicing variant in sepiapterin reductase deficiency: Are milder cases escaping diagnosis?
por: Nakagama, Yu, et al.
Publicado: (2019)

Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings
por: Ferreira, Patrick, et al.
Publicado: (2015)

Childhood choreoathetosis secondary to hyper-IgM syndrome (CD40 ligand deficiency)
por: Coulter, Ian C., et al.
Publicado: (2020)

Autoimmunity complicating SARS-CoV-2 infection in selective IgA-deficiency
por: Pfeuffer, Steffen, et al.
Publicado: (2020)

Modulation of SOD3 Levels Is Detrimental to Retinal Homeostasis
por: Ikelle, Larissa, et al.
Publicado: (2021)

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
por: Klepper, Joerg, et al.
Publicado: (2020)

COVID-19-associated ophthalmoparesis and hypothalamic involvement
por: Pascual-Goñi, Elba, et al.
Publicado: (2020)

Further supporting evidence for REEP1 phenotypic and allelic heterogeneity
por: Maroofian, Reza, et al.
Publicado: (2019)

Transient Receptor Potential Vanilloid in the Brain Gliovascular Unit: Prospective Targets in Therapy
por: Luo, Huilong, et al.
Publicado: (2021)

Targeting gliovascular connexins prevents inflammatory blood-brain barrier leakage and astrogliosis
por: De Bock, Marijke, et al.
Publicado: (2022)

Frontal white matter hyperintensities, clasmatodendrosis and gliovascular abnormalities in ageing and post-stroke dementia
por: Chen, Aiqing, et al.
Publicado: (2016)

Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation
por: Jaffer, Fatima, et al.
Publicado: (2017)

Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations
por: Lynch, David S., et al.
Publicado: (2017)

Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy
por: Bugiardini, Enrico, et al.
Publicado: (2017)

Sex-Dependent Gliovascular Interface Abnormality in the Hippocampus following Postnatal Immune Activation in Mice
por: Ardalan, Maryam, et al.
Publicado: (2022)

Gliovascular alterations in sporadic and familial Alzheimer's disease: APOE3 Christchurch homozygote glioprotection
por: Henao‐Restrepo, Julián, et al.
Publicado: (2022)

Frequency of GAA-FGF14 Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia
por: Novis, Luiz Eduardo, et al.
Publicado: (2023)

Late-onset Lafora disease with prominent parkinsonism due to a rare mutation in EPM2A
por: Lynch, David S., et al.
Publicado: (2016)

Autoimmune hemolytic anemia, demyelinating relapse, and AQP1 antibodies after alemtuzumab infusion
por: Tzartos, John S., et al.
Publicado: (2020)

Compound heterozygous mutations in MASP1 in a deaf child with absent cochlear nerves
por: Kari, Elina, et al.
Publicado: (2017)

1q21.1 Duplication syndrome and epilepsy: Case report and review
por: Gourari, Ioulia, et al.
Publicado: (2018)

Familial Lipomas Without Classic Neurofibromatosis-1 Caused by a Missense Germline NF1 Mutation
por: Ramirez, Erika, et al.
Publicado: (2021)

A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominance
por: Niu, Qi, et al.
Publicado: (2015)

Long-term improvement after combined immunomodulation in early post-H1N1 vaccination narcolepsy
por: Viste, Rannveig, et al.
Publicado: (2017)

Null mutation in SCN9A in which noxious stimuli can be detected in the absence of pain
por: Ramirez, Juan D., et al.
Publicado: (2014)

Independent NF1 mutations underlie café-au-lait macule development in a woman with segmental NF1
por: Freret, Morgan E., et al.
Publicado: (2018)

Antibodies to aquaporin-1 are not present in neuromyelitis optica
por: Schanda, Kathrin, et al.
Publicado: (2015)

FHF1 (FGF12) epileptic encephalopathy
por: Al-Mehmadi, Sameer, et al.
Publicado: (2016)

Missense mutations in DYT-TOR1A dystonia
por: Iqbal, Zafar, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_0gqtn75tc9vbght0bmqgf1v2fc