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Page 1
Detection of Gallbladder Disease Types Using Deep Learning: An Informative Medical Method.
Diagnostics (Basel). 2023 May 15;13(10):1744. doi: 10.3390/diagnostics13101744.
Diagnostics (Basel). 2023.
PMID: 37238227
Free PMC article.
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
Ksantini M, Lafont E, Bocquet B, Meunier I, Hamel CP.
Ksantini M, et al.
Eur J Ophthalmol. 2012 Jul-Aug;22(4):647-53. doi: 10.5301/ejo.5000096.
Eur J Ophthalmol. 2012.
PMID: 22180149
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Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations.
Ksantini M, Sénéchal A, Bocquet B, Meunier I, Brabet P, Hamel CP.
Ksantini M, et al.
Ophthalmic Genet. 2010 Dec;31(4):200-4. doi: 10.3109/13816810.2010.512354.
Ophthalmic Genet. 2010.
PMID: 21067480
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MEFV mutations in Tunisian patients suffering from familial Mediterranean fever.
Chaabouni HB, Ksantini M, M'rad R, Kharrat M, Chaabouni M, Maazoul F, Bahloul Z, Ben Jemaa L, Ben Moussa F, Ben Chaabane T, Mrad S, Touitou I, Smaoui N.
Chaabouni HB, et al. Among authors: ksantini m.
Semin Arthritis Rheum. 2007 Jun;36(6):397-401. doi: 10.1016/j.semarthrit.2006.12.004. Epub 2007 Feb 5.
Semin Arthritis Rheum. 2007.
PMID: 17276496
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UIdataGB: Multi-Class ultrasound images dataset for gallbladder disease detection.
Turki A, Obaid AM, Bellaaj H, Ksantini M, AlTaee A.
Turki A, et al. Among authors: ksantini m.
Data Brief. 2024 Apr 15;54:110426. doi: 10.1016/j.dib.2024.110426. eCollection 2024 Jun.
Data Brief. 2024.
PMID: 38708300
Free PMC article.
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RRH, encoding the RPE-expressed opsin-like peropsin, is not mutated in retinitis pigmentosa and allied diseases.
Ksantini M, Sénéchal A, Humbert G, Arnaud B, Hamel CP.
Ksantini M, et al.
Ophthalmic Genet. 2007 Mar;28(1):31-7. doi: 10.1080/13816810701202052.
Ophthalmic Genet. 2007.
PMID: 17454745
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