Results 41 to 50 of about 1,997 (169)

A Novel Application of Injectable PRF for Superior Sulcus Hollowing

open access: yesJournal of Cosmetic Dermatology, Volume 25, Issue 1, January 2026.
ABSTRACT Background Superior sulcus hollowing is a frequent esthetic concern, commonly managed with synthetic fillers or fat grafts; however, these approaches carry potential risks and costs. Injectable platelet‐rich fibrin (i‐PRF), an autologous regenerative biomaterial, has shown promise in dermatologic and dental applications, but its use for ...
Nese Arslan   +3 more
wiley   +1 more source

Evaluation of the Effectiveness of Excision Techniques from Cornea to Limbus and from Limbus to Cornea on Recurrence in Pterygium Surgery

open access: yesTürk Oftalmoloji Dergisi, 2014
Objectives: To evaluate the recurrence rates of two different pterygium excision procedures, i.e. “excision from the cornea to the limbus” and “excision from the limbus to the cornea”.
Tuba Çelik
doaj   +1 more source

Dry-Eye Disease in Recurrent Pterygium

open access: yesOphthalmic Research, 2018
<b><i>Purpose:</i></b> The aim of this paper was to investigate the degree of inflammation and dry-eye disease (DED) in recurrent pterygium. <b><i>Methods:</i></b> Fifty-five patients with a history of pterygium excision were divided into 3 groups – Group 1: no recurrence after the first excision; Group 2:
Jeremy, Tan   +3 more
openaire   +2 more sources

Unveiling Giant Onychomatricoma: A Diagnostic and Therapeutic Challenge

open access: yesCase Reports in Dermatological Medicine, Volume 2026, Issue 1, 2026.
Onychomatricoma is a rare benign tumor of the nail matrix that is often misdiagnosed due to its resemblance to other nail conditions, particularly onychomycosis. A giant variant, which affects the entire nail structure, is even more uncommon, with fewer than 20 cases documented.
Katherine Nicole Calderón Tiburcio   +4 more
wiley   +1 more source

Double Flip Technique for Graft Transfer in Autograft Pterygium Surgery

open access: yesTürk Oftalmoloji Dergisi, 2023
A 50-year-old man with recurrent pterygium and a 46-year-old woman with primary pterygium underwent surgery using a novel autograft transfer technique that facilitates autograft suturing and ensures correct graft orientation. After removing the pterygium,
Emrah Öztürk, Abuzer Gündüz
doaj   +1 more source

Beyond Tumor Control: A Protocol for Multidimensional Assessment of Long‐Term Effects of Intensity‐Modulated Radiotherapy on Vision, Patient Well‐Being, and Morbidity in Head and Neck Cancer

open access: yes
Med Research, Volume 2, Issue 1, Page 190-194, March 2026.
Benjamin Abaidoo   +6 more
wiley   +1 more source

Expanding the Clinical Spectrum of Bruck Syndrome: A Case Report and Literature Review

open access: yesCase Reports in Pediatrics, Volume 2026, Issue 1, 2026.
Background Bruck syndrome is a rare autosomal recessive disorder characterized by osteogenesis imperfecta–like bone fragility and congenital joint contractures. Clinical overlap with other connective tissue disorders makes early diagnosis challenging, and genetic testing remains essential.
Ansam Nafah   +5 more
wiley   +1 more source

Outcome of intraoperative use of mitomycin C combined with conjunctival auto graft in recurrent pterygium

open access: yesIMC Journal of Medical Science, 2016
Background and objectives: Recurrent pterygium is an important ocular problem in our country. There are different modalities of treatment for recurrent pterygium.
MK Goswami   +3 more
doaj  

Congenital Syngnathia With Holoprosencephaly: A Case Report of a Fatal Presentation in a Resource‐Limited Setting

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Congenital syngnathia, the rare fusion of the maxilla and mandible, poses significant feeding and respiratory challenges. Its management is complicated by rarity and potential syndromic associations. We present a 1‐week‐old female neonate who presented with left jaw deviation, respiratory distress (SpO2 69%, tachypnea), and fever.
Asteway M. Haile   +5 more
wiley   +1 more source

Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher   +6 more
wiley   +1 more source

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