Publications by authors named "Ilka Huber"

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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia.
Scott Barish, Sheng-Jia Lin, Reza Maroofian, Alper Gezdirici, Hamoud Alhebby, Ilka Huber

Am J Hum Genet· November 2024

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Further delineation of Malan syndrome.
Manuela Priolo, Denny Schanze, Katrin Tatton-Brown, Paul A Mulder, Jair Tenorio, Ilka Huber

Hum Mutat· September 2018

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Direct Molecular Detection and Genotyping of Borrelia burgdorferi Sensu Lato in Cerebrospinal Fluid of Children with Lyme Neuroborreliosis.
Bjørn Barstad, Hanne Quarsten, Dag Tveitnes, Sølvi Noraas, Ingvild S Ask, Ilka Huber

J Clin Microbiol· May 2018

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Cerebrospinal Fluid B-lymphocyte Chemoattractant CXCL13 in the Diagnosis of Acute Lyme Neuroborreliosis in Children.
Bjørn Barstad, Dag Tveitnes, Sølvi Noraas, Ingvild Selvik Ask, Maryam Saeed, Ilka Huber

Pediatr Infect Dis J· December 2017

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A suggestive association of fuchs heterochromic cyclitis with cytotoxic T cell antigen 4 gene polymorphism.
Bernd M Spriewald, Carolina Lefter, Ilka Huber, Birgit Lauer, Hartmut Wenkel

Ophthalmic Res· May 2007

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