Pediatric Multiple Sclerosis
What's New
Last Posted: Mar 06, 2023
- Prevalence of salivary human herpesviruses in pediatric multiple sclerosis cases and controls.
Leibovitch Emily C, et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2018 0 (5) 644-652 - The contribution of secondhand tobacco smoke exposure to pediatric multiple sclerosis risk.
Lavery Amy M, et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2018 0 (4) 515-522 - HLA-DRB1 allele impact on pediatric multiple sclerosis in a Hellenic cohort.
Gontika Maria, et al. Multiple sclerosis journal - experimental, translational and clinical 2020 0 (1) 2055217320908046 - Age-related blood transcriptional regulators affect disease progression in pediatric multiple sclerosis.
Shavit Eitan, et al. Neurobiology of disease 2022 0 105953 - Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis.
Greenberg Benjamin M et al. Neurology(R) neuroimmunology & neuroinflammation 2021 8(5) - Antibody response to common viruses and human leukocyte antigen-DRB1 in pediatric multiple sclerosis.
Waubant Emmanuelle, et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2013 6 (7) 891-5 - Copy number variation in pediatric multiple sclerosis.
McElroy J, et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2012 12 - Common viruses associated with lower pediatric multiple sclerosis risk.
Waubant E, et al. Neurology 2011 6 (23) 1989-95 - Pediatric multiple sclerosis
From NCATS Genetic and Rare Diseases Information Center
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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