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KARLA SALAZAR

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Aduru C, Chandrasekar A, Blasingame K, Rosen J, Levine JM, Salazar K, Chilakapati M, Foroozan R, Adeseye V, Yarimi JM, Shukla N, Lotze TE, Fisher KS, Sandweiss AJ. Reply to: A Lethal Progressive Neuroinflammation Disguised as MOGAD Revealing a Final Diagnosis of Griscelli Syndrome: Regarding: MOGAD is the Most Common Cause of Isolated Optic Neuritis in Children. Ann Clin Transl Neurol. 2026 Aug; 13(8):1743-1744. PMID: 42370698; PMCID: PMC13394892.
      Citations:    Fields:    
    2. Aduru C, Chandrasekar A, Blasingame K, Rosen J, Levine JM, Salazar K, Chilakapati M, Foroozan R, Hardwick V, Yarimi JM, Shukla N, Lotze TE, Fisher KS, Sandweiss AJ. MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children. Ann Clin Transl Neurol. 2026 May 04. PMID: 42080421; PMCID: PMC13394016.
      Citations:    Fields:    
    3. Rossi V, Brooks D, Dai H, Mizerik E, Salazar K, Davila-Williams D, Ben-Moshe Y, Lalani SR, Elsea SH, Gijavanekar C, Scott DA, Machol K, Bekheirnia MR, Scaglia F. A Rare Molecular Diagnosis in a Patient With Hepatocerebral Syndrome Contributes to the Expansion of the Phenotypic Spectrum of POLG2 -Related Mitochondrial Disorder. Am J Med Genet A. 2025 11; 197(11):e64177. PMID: 40631390.
      Citations:    Fields:    Translation:Humans
    4. El Atrache R, Mizerik M, Ruiz Lopez JF, Engstrom E, Salazar KP, Guzman-Karlsson MC, Davila-Williams D, Sen S, Fisher KS, Erklauer JC. Intracranial Rhizomucor Pusillus Mucormycosis in an Adolescent Triggering a Stroke Alert: A Case Report and a Systematic Review of Pediatric Cases. J Child Neurol. 2025 09; 40(8):678-685. PMID: 40329649; PMCID: PMC12332211.
      Citations:    Fields:    Translation:HumansAnimals
    5. Yarimi JM, Sandweiss AJ, Salazar KP, Massrey C, Ankar A, Muscal E, Lai YC, Cokley JA, Davila-Williams D, Shukla NM, Fisher KS. IT-DEX and B cell depletion in a child with anti-GAD 65 autoimmune encephalitis presenting as NORSE: A case report. J Neuroimmunol. 2024 10 15; 395:578430. PMID: 39128431.
      Citations: 2     Fields:    Translation:HumansCells
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