Diagnostic ophthalmology. Congenital stationary night blindness (CSNB).

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Citations

1. May-Davis S, Dzingle D, Saber E, Blades Eckelbarger P. Characterization of the Caudal Ventral Tubercle in the Sixth Cervical Vertebra in Modern Equus ferus caballus. Animals (Basel) 2023 Jul 22;13(14).
   doi: 10.3390/ani13142384pubmed: 37508161google scholar: lookup
2. Miraldi Utz V, Pfeifer W, Longmuir SQ, Olson RJ, Wang K, Drack AV. Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children. JAMA Ophthalmol 2018 Apr 1;136(4):389-398.
   doi: 10.1001/jamaophthalmol.2018.0185pubmed: 29522070google scholar: lookup
3. Bagheri A, Persano Adorno D, Rizzo P, Barraco R, Bellomonte L. Empirical mode decomposition and neural network for the classification of electroretinographic data. Med Biol Eng Comput 2014 Jul;52(7):619-28.
   doi: 10.1007/s11517-014-1164-8pubmed: 24923413google scholar: lookup
4. Audo I, Kohl S, Leroy BP, Munier FL, Guillonneau X, Mohand-Saïd S, Bujakowska K, Nandrot EF, Lorenz B, Preising M, Kellner U, Renner AB, Bernd A, Antonio A, Moskova-Doumanova V, Lancelot ME, Poloschek CM, Drumare I, Defoort-Dhellemmes S, Wissinger B, Léveillard T, Hamel CP, Schorderet DF, De Baere E, Berger W, Jacobson SG, Zrenner E, Sahel JA, Bhattacharya SS, Zeitz C. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet 2009 Nov;85(5):720-9.
   doi: 10.1016/j.ajhg.2009.10.013pubmed: 19896113google scholar: lookup