Results 61 to 70 of about 1,419,074 (183)
Pathology Of “Post-Upper Blepharoplasty Syndrome”: Implications For Upper Eyelid Reconstruction
Clinical Ophthalmology, 2019 Kenneth D Steinsapir,1 Yoon-Duck Kim2 1Orbital and Ophthalmic Plastic Surgery Division, UCLA Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; 2Oculoplastic and Orbital Surgery Division, Department of Ophthalmology ...
Steinsapir KD, Kim YD
doaj
LifeThis study investigates the effects of levator advancement, with and without upper blepharoplasty, on dry-eye symptoms in patients with unilateral ptosis.
Dolika D. Vasović +11 more
doaj +1 more source
Evaluation of Thread Lifts With High‐Frequency Ultrasound
Journal of Ultrasound in Medicine, Volume 45, Issue 10, Page 2371-2379, October 2026.The number of esthetic procedures performed worldwide has been steadily increasing, including the growing use of thread lifts. As procedural volume grows, so does the need for imaging‐based evaluation of thread lifts. High‐frequency ultrasound (HFUS) provides high‐resolution imaging of facial structures, allowing accurate assessment of thread ...
Luciana C. Zattar +1 more
wiley +1 more source
An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]
, 1981 An 81-year-old man from a family with a history of oculopharyngeal muscular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65.
Krause, Klaus-Henning, Schmitt, H.-P.
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Clinical Ophthalmology, 2020 Aastha Gandhi,1 Anuj Mehta,1 Mayuresh Naik2 1Department of Ophthalmology, V.M.M.C & Safdarjung Hospital, Ansari Nagar, New Delhi 110029, India; 2Department of Ophthalmology, H.I.M.S.R & H.A.H.
Gandhi A, Mehta A, Naik M
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Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature
Clinical Genetics, Volume 110, Issue 4, Page 480-486, October 2026.Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi +6 more
wiley +1 more source
Adult-onset bulbar ptosis in Joubert syndrome [PDF]
, 2012 Benjamin Burt, Johanan Levine, Kim LeTexas Tech University, Department of Ophthalmology, Paul L Foster School of Medicine, El Paso, TexasAbstract: In this case report, we describe a case of adult-onset bulbar ptosis in a patient with Joubert syndrome ...
Le K, Burt B, Levine J
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Ptosis postcardiac surgery: a case of pituitary apoplexy
, 2002 We present a patient in whom ptosis and third cranial nerve palsy developed postcoronary artery bypass grafting, and discuss the management of pituitary apoplexy postcardiac ...
Ohri, Sunil K. +7 more
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Journal of Cosmetic Dermatology, Volume 25, Issue 10, October 2026.ABSTRACT Introduction Intradermal botulinum toxin type A (BoNT‐A; microtoxin) has been shown to improve skin texture, superficial rhytides, and sweat/sebaceous activity through neuronal (cholinergic) and non‐neuronal pathways. While discussions around immune system interactions for BoNT‐A in aesthetic indications exist for intramuscular injection, the ...
Je‐Young Park +6 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder that affects multiple organ systems, most commonly the skin, peripheral nerves, and skeletal system. However, involvement of the anterior mediastinum is rare and has been sporadically reported in the literature.
Yuhao Qi +4 more
wiley +1 more source