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Author/Creator Leroy, Bart P.

2. An Augmented ABCA4 Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients. Issue 1 (January 2015)

Authors:
Bauwens, Miriam; De Zaeytijd, Julie; Weisschuh, Nicole; Kohl, Susanne; Meire, Françoise; Dahan, Karin; Depasse, Fanny; De Jaegere, Sarah; De Ravel, Thomy; De Rademaeker, Marjan; Loeys, Bart; Coppieters, Frauke; Leroy, Bart P.; De Baere, Elfride
Journal:
Human mutation
Issue:
Volume 36:Issue 1(2015:Jan.)
Page Start:
39
Record Type:
Journal Article
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4. Broad locations of antigenic regions for anti-TRPM1 autoantibodies in paraneoplastic retinopathy with retinal ON bipolar cell dysfunction. (November 2021)

Authors:
Gyoten, Daichi; Ueno, Shinji; Okado, Satoshi; Chaya, Taro; Yasuda, Shunsuke; Morimoto, Takeshi; Kondo, Mineo; Kimura, Kazuhiro; Hayashi, Takaaki; Leroy, Bart P.; Woo, Se Joon; Mukai, Ryo; Joo, Kwangsic; Furukawa, Takahisa
Journal:
Experimental eye research
Issue:
Volume 212(2021)
Page Start:
Record Type:
Journal Article
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5. CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up Study. Issue 1 (January 2021)

Authors:
Nguyen, Xuan-Thanh-An; Talib, Mays; van Cauwenbergh, Caroline; van Schooneveld, Mary J.; Fiocco, Marta; Wijnholds, Jan; ten Brink, Jacoline B.; Florijn, Ralph J.; Schalij-Delfos, Nicoline E.; Dagnelie, Gislin; van Genderen, Maria M.; de Baere, Elfride; Meester-Smoor, Magda A.; De Zaeytijd, Julie;...
Journal:
Retina
Issue:
Volume 41:Issue 1(2021)
Page Start:
Record Type:
Journal Article
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6. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021)

Authors:
Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend...
Journal:
Human mutation
Issue:
Volume 42:Issue 2(2021)
Page Start:
ii
Record Type:
Journal Article
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8. Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization. (1st October 2016)

Authors:
Fuerst, Nicole M.; Serrano, Leona; Han, Grace; Morgan, Jessica I. W.; Maguire, Albert M.; Leroy, Bart P.; Kim, Benjamin J.; Aleman, Tomas S.
Journal:
Ophthalmic genetics
Issue:
Volume 37:Number 4(2016)
Page Start:
445
Record Type:
Journal Article
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10. Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in ASPH. (4th July 2021)

Authors:
Van Hoorde, Tom; Nerinckx, Fanny; Kreps, Elke; Roels, Dimitri; Huyghe, Philippe; Van Heetvelde, Mattias; Verdin, Hannah; De Baere, Elfride; Balikova, Irina; Leroy, Bart P.
Journal:
Ophthalmic genetics
Issue:
Volume 42:Number 4(2021)
Page Start:
493
Record Type:
Journal Article
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