Academic Bibliography

Search 200 years of publications by Ghent University researchers.

dr. Kimberley Stee

Faculty of Veterinary Medicine > Department of Small animals

Work address: Salisburylaan 133, D4 ingang 20
9820 Merelbeke
Email: Kimberley.Stee@UGent.be

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Spinocerebellar ataxia in the Bouvier des Ardennes breed is caused by a KCNJ10 missense variant

Kimberley Stee (UGent) , Mario Van Poucke (UGent) , Martí Pumarola, Lise Geerinckx, Iris Van Soens, Sofie Bhatti (UGent) , Luc Peelman (UGent) and Ine Cornelis (UGent)

(2022) JOURNAL OF VETERINARY INTERNAL MEDICINE.
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Chronic vertebral Escherichia coli osteomyelitis in a 4-year-old dog

Veerle Hertog, Femke Mortier (UGent) , Kimberley Stee (UGent) and Emmelie Stock (UGent)

(2022) VETERINARY RECORD CASE REPORTS. 10(2).
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Paradoxical pseudomyotonia in English Springer and Cocker Spaniels

Kimberley Stee (UGent) , Mario Van Poucke (UGent) , Luc Peelman (UGent) and Mark Lowrie

(2020) JOURNAL OF VETERINARY INTERNAL MEDICINE. 34(1). p.253-257
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Truncating SLC12A6 variants cause different clinical phenotypes in humans and dogs

Mario Van Poucke (UGent) , Kimberley Stee (UGent) , Laurien Sonck (UGent) , Emmelie Stock (UGent) , Leslie Bosseler, Jo Van Dorpe (UGent) , Filip Van Nieuwerburgh (UGent) , Dieter Deforce (UGent) , Luc Peelman (UGent) , Luc Van Ham (UGent) , et al.

(2019) EUROPEAN JOURNAL OF HUMAN GENETICS. 27(10). p.1561-1568
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Imepitoin withdrawal in dogs with idiopathic epilepsy well-controlled with imepitoin and phenobarbital and/or potassium bromide does not increase seizure frequency

Kimberley Stee (UGent) , Valentine Martlé (UGent) , Bart Broeckx (UGent) , Emilie Royaux, Luc Van Ham (UGent) and Sofie Bhatti (UGent)

(2017) VETERINARY JOURNAL. 230. p.1-5
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The novel homozygous KCNJ10 c.986T > C (p.(Leu329Pro)) variant is pathogenic for the SeSAME/EAST homologue in Malinois dogs

Mario Van Poucke (UGent) , Kimberley Stee (UGent) , Sofie Bhatti (UGent) , An Vanhaesebrouck, Leslie Bosseler, Luc Peelman (UGent) and Luc Van Ham (UGent)

(2017) EUROPEAN JOURNAL OF HUMAN GENETICS. 25(2). p.222-226