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1976 1
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Ultrasound biomicroscopic study of anterior segment changes after phacoemulsification and foldable intraocular lens implantation.
Pereira FA, Cronemberger S. Pereira FA, et al. Ophthalmology. 2003 Sep;110(9):1799-806. doi: 10.1016/S0161-6420(03)00623-7. Ophthalmology. 2003. PMID: 13129880 Clinical Trial.
DESIGN: Prospective, nonrandomized, comparative (self-controlled) trial. PARTICIPANTS: Twenty-one eyes of 19 patients with senile or presenile cataracts and no other ocular illness. ...CONCLUSIONS: After phacoemulsification and foldable IOL implantation, UBM …
DESIGN: Prospective, nonrandomized, comparative (self-controlled) trial. PARTICIPANTS: Twenty-one eyes of 19 patients with senile or …
Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized.
Lorincz MT, Rainier S, Thomas D, Fink JK. Lorincz MT, et al. Arch Neurol. 2005 Sep;62(9):1459-63. doi: 10.1001/archneur.62.9.1459. Arch Neurol. 2005. PMID: 16157755
BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is a rare but treatable neurodegenerative disorder caused by 27-sterol hydroxylase (CYP27) deficiency. OBJECTIVE: To describe clinical features and results of genetic analysis in a family with CTX. ...RESULTS: The proband an …
BACKGROUND: Cerebrotendinous xanthomatosis (CTX) is a rare but treatable neurodegenerative disorder caused by 27-sterol hydroxylase (CYP27) …
Pars plana vitrectomy. Microsurgical pars plana lensectomy.
Douvas NG. Douvas NG. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol. 1976 May-Jun;81(3 Pt 1):371-81. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol. 1976. PMID: 960359
It is to be considered as a method of choice for the removal of presenile cataracts in patients under the age of 40, developmental cataracts, cataracta complicata secondary to uveitis, subluxated and luxated cataracts. ...
It is to be considered as a method of choice for the removal of presenile cataracts in patients under the age of 40, developme …
Learning from errors: when a low platelet count in neonate excludes immune thrombocytopenic purpura in mother.
Gresikova M. Gresikova M. Bratisl Lek Listy. 2013;114(4):232-6. doi: 10.4149/bll_2013_048. Bratisl Lek Listy. 2013. PMID: 23514558
Particular attention is paid to inborn macrothrombocytopenia without congenital anomalies. They represent a rare group of diseases, often captured randomly or during routine examinations. An attention is paid on congenital macrothrombocytopenia variants with mutations in t …
Particular attention is paid to inborn macrothrombocytopenia without congenital anomalies. They represent a rare group of diseases, often ca …