Results 131 to 140 of about 29,128 (218)

Xeno-ADM combined with inferior eyelid margin fixation to treat entropion accompanied by lower eyelid retraction. [PDF]

BMC Ophthalmol
Fang Y, Lai Y, Liao H, Huang Q.
europepmc   +1 more source

Intraocular incarceration of eyelash

Indian Journal of Ophthalmology, 2020
Kumar, Karthik, Ravindran, Ram S, Kannan, Naresh B   +2 more
openaire   +2 more sources

The Hidden Culprit Unraveled by Dermoscopy: A Rare Case of Pediatric Facial Demodicosis. [PDF]

Cureus
Bouhamdi C, Baybay H, Soughi M, Elloudi S, Mernissi FZ.   +4 more
europepmc   +1 more source

Knowledge, Awareness, and Perceptions of Artificial Eyelash Use and Associated Ocular Side Effects Among Palestinian Females: A Cross-Sectional Study. [PDF]

Cureus
Beshtawi IM, Walweel D, Sakhel W, Shashtare A.   +3 more
europepmc   +1 more source

Clinical efficacy of an improved orbicularis oculi muscle plication surgery for senile involutional lower eyelid entropion. [PDF]

Int Ophthalmol
Peng D, Gu W, Wang Z.
europepmc   +1 more source

An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery. [PDF]

Clin Cosmet Investig Dermatol
Ghaznavi A, Borooghani H, Pahlevan Sabagh A, Aghajanlou T.   +3 more
europepmc   +1 more source

ASXL3 gene variants causing Bainbridge-Ropers syndrome: clinical and genetic analysis of four Chinese patients. [PDF]

Front Neurosci
Yang Q, Zhang Q, Zhou X, Yi S, Qin Z, Yi S, He S, Luo J.   +7 more
europepmc   +1 more source

Case Report: Rothmund-Thomson syndrome type 2 in Ecuador: clinical and molecular insights into a recurrent <i>RECQL4</i> variant. [PDF]

Front Pediatr
Armas Samaniego MI, Briones Vasquez M, Mariño Zambrano M, Romero VI, Melo K, Pozo-Palacios JC.   +5 more
europepmc   +1 more source

Infestation of eyelashes by Pediculus humanus capitis (family: pediculidae): a case report. [PDF]

J Med Case Rep
Abbasi M, Yousefi S.
europepmc   +1 more source

Neuronal Heterotopy in a Patient with Wiedemann-Steiner Syndrome Caused by a Truncating <i>KMT2A</i> Variant: Clinical and Genetic Correlations. [PDF]

Reports (MDPI)
Sokolova T, Ivanov H, Panova M, Sotkova-Ivanova I, Stoyanova V.   +4 more
europepmc   +1 more source