Results 31 to 40 of about 83,153 (169)
Primary posterior capsulorexis: historical aspects and the current state of the issue
Purpose. The paper analyzes the data of modern literature (published from 2008 to 2023) on the history and technique of primary posterior capsulorexis (PPC). The fields of application, variations, effectiveness and safety of the procedure are considered.
E.V. Egorova, A.O. Direev
doaj +1 more source
Introduction: Leber hereditary optic neuropathy (LHON) complicated with extraocular symptoms is called LHON plus. We describe a case of LHON plus with a rare mutation, which also caused dystonia.
Fumio Takano +7 more
doaj +1 more source
Nkx6.1 and Isl1 function as antagonistic transcriptional regulators of the Arx Re1 enhancer.
Immunofluorescence staining of pancreata from Ngn3-Cre;Z/EG mice at e14.5 (A) and e16.5 (B) for Nkx6.1, Arx, and GFP shows that the majority of progeny of Ngn3-expressing cells (GFP+) co-express Arx and Nkx6.1 at e14.5 (arrowheads in A), while the Arx ...
Klaus H. Kaestner (123518) +11 more
core +1 more source
Abstract Book: 25th Congress of the European Hematology Association Virtual Edition, 2020
HemaSphere, Volume 4, Issue S1, Page 1-1168, June 2020.
wiley +1 more source
Purpose: To assess the performance of a hybrid Transformer-based convolutional neural network (CNN) model for automated detection of keratoconus in stand-alone Scheimpflug-based dynamic corneal deformation videos (DCDVs).
Hazem Abdelmotaal +8 more
doaj +1 more source
RADIOSENSITIZATION OF GLIOMA TUMOR CELLS USING Cl-994 (N-ACETYLDINALINE)
Radiation therapy continues to be a primary treatment modality for solid tumors. The development of agents that can enhance tumor cell radiosensitivity may thus provide patients a significant advantage.
Burgan, William E. Jr.
core +1 more source
Purpose: This study aims to evaluate the central corneal thickness (CCT), intraocular pressure (IOP), and glycemic status in uncontrolled diabetic patients at baseline, 1 week, and 12 weeks, and to examine the relationship between changes in CCT and IOP ...
Vaisna Gopi +2 more
doaj +1 more source
Type 1 neurofibromatosis (NF1) is an autosomal dominant multisystem disease caused by a mutation in the neurofibromin 1 gene, which affects tissues derived from the neural crest.
Sujit Das
doaj +1 more source

