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Page 1
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Oztürk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkäemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF 3rd, Engle EC. Yamada K, et al. Among authors: zwaan jt. Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23. doi: 10.1167/iovs.03-1413. Invest Ophthalmol Vis Sci. 2004. PMID: 15223798
Pyramidal anterior polar cataracts.
Wheeler DT, Mullaney PB, Awad A, Zwaan J. Wheeler DT, et al. Ophthalmology. 1999 Dec;106(12):2362-7. doi: 10.1016/S0161-6420(99)90540-7. Ophthalmology. 1999. PMID: 10599671
Glaucoma in Sturge-Weber syndrome.
Awad AH, Mullaney PB, Al-Mesfer S, Zwaan JT. Awad AH, et al. Among authors: zwaan jt. J AAPOS. 1999 Feb;3(1):40-5. doi: 10.1016/s1091-8531(99)70093-5. J AAPOS. 1999. PMID: 10071900
Pediatric IOL implantation: the KKESH experience.
Wheeler DT, Mullaney PB, Awad A, al-Mesfer S, al-Nahdi T, Zwaan J. Wheeler DT, et al. J Pediatr Ophthalmol Strabismus. 1997 Nov-Dec;34(6):341-6. doi: 10.3928/0191-3913-19971101-05. J Pediatr Ophthalmol Strabismus. 1997. PMID: 9430060
55 results