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Ophthalmologic findings in Usher syndrome type 2A.
Van Aarem A, Wagenaar M, Pinckers AJ, Huygen PL, Bleeker-Wagemakers EM, Kimberling BJ, Cremers CW. Van Aarem A, et al. Among authors: pinckers aj. Ophthalmic Genet. 1995 Dec;16(4):151-8. doi: 10.3109/13816819509057856. Ophthalmic Genet. 1995. PMID: 8749051
The Usher syndrome type 2A: clinical findings in obligate carriers.
van Aarem A, Cremers CW, Pinckers AJ, Huygen PL, Hombergen GC, Kimberling BJ. van Aarem A, et al. Among authors: pinckers aj. Int J Pediatr Otorhinolaryngol. 1995 Mar;31(2-3):159-74. doi: 10.1016/0165-5876(94)01081-8. Int J Pediatr Otorhinolaryngol. 1995. PMID: 7782174
Stable and progressive hearing loss in type 2A Usher's syndrome.
van Aarem A, Pinckers AJ, Kimberling WJ, Huygen PL, Bleeker-Wagemakers EM, Cremers CW. van Aarem A, et al. Among authors: pinckers aj. Ann Otol Rhinol Laryngol. 1996 Dec;105(12):962-7. doi: 10.1177/000348949610501206. Ann Otol Rhinol Laryngol. 1996. PMID: 8973283
Clinical findings in obligate carriers of type I Usher syndrome.
Wagenaar M, ter Rahe B, van Aarem A, Huygen P, Admiraal R, Bleeker-Wagemakers E, Pinckers A, Kimberling W, Cremers C. Wagenaar M, et al. Am J Med Genet. 1995 Nov 20;59(3):375-9. doi: 10.1002/ajmg.1320590319. Am J Med Genet. 1995. PMID: 8599365
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis).
Taschner PE, de Vos N, Post JG, Meijers-Heijboer EJ, Hofman I, Loonen MC, Pinckers AJ, Bleeker-Wagemakers EM, Gardiner RM, Breuning MH. Taschner PE, et al. Among authors: pinckers aj. Am J Med Genet. 1995 Jun 5;57(2):333-7. doi: 10.1002/ajmg.1320570246. Am J Med Genet. 1995. PMID: 7668358 Free article.
Atypical Cogan's syndrome: an autoimmune disease?
Peeters GJ, Cremers CW, Pinckers AJ, Hoefnagels WH. Peeters GJ, et al. Among authors: pinckers aj. Ann Otol Rhinol Laryngol. 1986 Mar-Apr;95(2 Pt 1):173-5. doi: 10.1177/000348948609500213. Ann Otol Rhinol Laryngol. 1986. PMID: 3963689
147 results