Rotsos相关文献与解析，生知库 | 链接生命科学的每一步

Reply to Dr Kemal Örnek Regarding Comments on: "Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy"

回复 Kemal Örnek 博士关于以下评论：“MTHFR 基因 C6777T 突变和凝血酶原基因 FII G20210A 突变的复合杂合性在连续性双侧前部缺血性视神经病变中的作用”

doi:10.1080/01658107.2025.2575369

Tsiogka, Anastasia; Vlachos, Georgios; Galanopoulos, Athanasios; Rotsos, Tryfon; Kandarakis, Stylianos; Nikolopoulou, Anthi; Karmiris, Efthymios; Chatzistefanou, Klio I

发表日期：2026

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Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy

MTHFR基因C6777T突变和凝血酶原基因FII G20210A突变的复合杂合性导致双侧前部缺血性视神经病变

期刊:Neuro-Ophthalmology

影响因子:0.8

doi:10.1080/01658107.2024.2402725

Tsiogka, Anastasia; Vlachos, Georgios; Galanopoulos, Athanasios; Rotsos, Tryfon; Kandarakis, Stylianos; Nikolopoulou, Anthi; Karmiris, Efthymios; Chatzistefanou, Klio I

发表日期：2025

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Retinal capillary plexus in Parkinson's disease using optical coherence tomography angiography

利用光学相干断层扫描血管造影术研究帕金森病患者的视网膜毛细血管丛

期刊:International Journal of Ophthalmology

影响因子:1.8

doi:10.18240/ijo.2024.01.18

Giachos, Ioannis; Doumazos, Spyridon; Tsiogka, Anastasia; Manoli, Konstantina; Tagaris, George; Rotsos, Tryfon; Kozobolis, Vassilios; Iliopoulos, Ioannis; Moschos, Marilita

The rare diagnosis of Von Hippel-Lindau disease in a 29-year-old patient

一名29岁患者被罕见地诊断出患有冯·希佩尔-林道综合征

期刊:Oman Journal of Ophthalmology

影响因子:

doi:10.4103/ojo.ojo_161_22

Rotsos, Tryfon; Bouzika, Peggy; Sotirianakou, Maria-Evanthia; Symeonidis, Chrysanthos; Giachos, Ioannis; Papakonstantinou, Evangelia; Paraskevopoulos, Theodoros; Georgalas, Ilias

发表日期：2024

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A 30-Year-Old Man with a Recent History of COVID-19 Requiring Treatment with Corticosteroids Who Developed Bilateral Central Serous Chorioretinopathy During 7-Month Follow-Up

一名30岁男性，近期有新冠肺炎病史，需要使用皮质类固醇治疗，在7个月的随访期间出现双侧中心性浆液性脉络膜视网膜病变。

期刊:American Journal of Case Reports

影响因子:0.7

doi:10.12659/AJCR.940241

Angelidis, Constantine D; Georgalas, Ilias; Giachos, Ioannis; Symeonidis, Chrysanthos; Mani, Aikaterini; Rotsos, Tryfon

Wolfram Syndrome: A case report of two sisters Wolfram Syndrome: Case report of two sisters

沃尔夫拉姆综合征：两姐妹的病例报告

期刊:American Journal of Ophthalmology Case Reports

影响因子:

doi:10.1016/j.ajoc.2022.101452

Rotsos, Tryfon; Papakonstantinou, Evangelia; Symeonidis, Chrysanthos; Krassas, Augoustinos; Kamakari, Smaragda

发表日期：2022

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Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophy

扩展 PRPF8、PRPH2、RP1 和 RPGR 的表型谱，以及早发性严重视网膜营养不良的基因型谱

期刊:Orphanet Journal of Rare Diseases

影响因子:3.5

doi:10.1186/s13023-021-01759-8

Georgiou, Michalis; Ali, Naser; Yang, Elizabeth; Grewal, Parampal S; Rotsos, Tryfon; Pontikos, Nikolas; Robson, Anthony G; Michaelides, Michel

发表日期：2021

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Epiretinal membrane-induced intraretinal neovascularization

视网膜前膜诱导的视网膜内新生血管

期刊:American Journal of Ophthalmology Case Reports

影响因子:

doi:10.1016/j.ajoc.2021.101180

Giachos, Ioannis; Chalkiadaki, Evangelia; Andreanos, Konstantinos; Symeonidis, Chrysanthos; Charonis, Alexandros; Georgalas, Ilias; Rotsos, Tryfon

发表日期：2021

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A fingerprint hidden inside the eye. A unique pattern of outer retina splitting as seen on en-face OCT and OCT-angiography

眼内隐藏的指纹。在OCT和OCT血管造影中可见独特的视网膜外层分裂模式。

期刊:American Journal of Ophthalmology Case Reports

影响因子:

doi:10.1016/j.ajoc.2021.101184

Rotsos, Tryfon; Symeonidis, Chrysanthos; Kanakis, Menelaos; Andreanos, Konstantinos

发表日期：2021

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Management of fibrosis in neovascular age-related macular degeneration

新生血管性年龄相关性黄斑变性中纤维化的治疗

Reply to Dr Kemal Örnek Regarding Comments on: "Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy"

回复 Kemal Örnek 博士关于以下评论：“MTHFR 基因 C6777T 突变和凝血酶原基因 FII G20210A 突变的复合杂合性在连续性双侧前部缺血性视神经病变中的作用”

Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy

MTHFR基因C6777T突变和凝血酶原基因FII G20210A突变的复合杂合性导致双侧前部缺血性视神经病变

Retinal capillary plexus in Parkinson's disease using optical coherence tomography angiography

利用光学相干断层扫描血管造影术研究帕金森病患者的视网膜毛细血管丛

The rare diagnosis of Von Hippel-Lindau disease in a 29-year-old patient

一名29岁患者被罕见地诊断出患有冯·希佩尔-林道综合征

A 30-Year-Old Man with a Recent History of COVID-19 Requiring Treatment with Corticosteroids Who Developed Bilateral Central Serous Chorioretinopathy During 7-Month Follow-Up

一名30岁男性，近期有新冠肺炎病史，需要使用皮质类固醇治疗，在7个月的随访期间出现双侧中心性浆液性脉络膜视网膜病变。

Wolfram Syndrome: A case report of two sisters Wolfram Syndrome: Case report of two sisters

沃尔夫拉姆综合征：两姐妹的病例报告

Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophy

扩展 PRPF8、PRPH2、RP1 和 RPGR 的表型谱，以及早发性严重视网膜营养不良的基因型谱

Epiretinal membrane-induced intraretinal neovascularization

视网膜前膜诱导的视网膜内新生血管

A fingerprint hidden inside the eye. A unique pattern of outer retina splitting as seen on en-face OCT and OCT-angiography

眼内隐藏的指纹。在OCT和OCT血管造影中可见独特的视网膜外层分裂模式。