Results 161 to 170 of about 114,602 (311)

Lateral Tarsorrhaphy and Fixation on the Orbital Ligament to Correct Macroblepharon in Dogs: 77 Palpebral Fissures

open access: yesVeterinary Ophthalmology, Volume 28, Issue 2, Page 448-456, March 2025.
ABSTRACT Purpose To describe a surgical method for correcting lower lid entropion, lateral canthal entropion, and macroblepharon. Methods Lid margins were incised at a 45° angle, and lateral lid margins and a rhomboid shaped piece of skin were resected based on the degree of macroblepharon.
Maximilian Werner‐Tutschku   +1 more
wiley   +1 more source

Gonadal Histology and Spawning Season of Otolithoides pama in the Thanlwin River Estuary

open access: yesAquaculture, Fish and Fisheries, Volume 6, Issue 3, June 2026.
ABSTRACT The spawning season of Otolithoides pama in the Thanlwin estuary was estimated through gonadosomatic index (GSI) and histological analyses of gonadal development. A total of 290 specimens (240 females and 50 males) were collected monthly from 5 sites—Ahlat, Kyauk Tan, Daye, Nyaung Pin Seik and Tarana—between January and December 2024.
Thet Htwe Aung
wiley   +1 more source

Outcome analysis of major cardiac operations in low weight neonates [PDF]

open access: yes, 2004
Bové, Thierry   +10 more
core   +2 more sources

TRICUSPID ATRESIA [PDF]

open access: yesHeart, 1956
J W, BROWN   +3 more
openaire   +2 more sources

From Multiple Congenital Anomalies to Pituitary Gland Malformation: Wide Spectrum of Clinical Features in a Family With FOXA2 Variant

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1452-1457, June 2026.
ABSTRACT FOXA2 (hepatocyte nuclear factor‐3β, HNF‐3β) encodes a transcriptional activator involved in early embryogenesis, particularly in the patterning and differentiation of midline structures such as the neural tube, foregut, and pituitary gland. Its role in human pathogenesis was first suspected when patients with deletion of chromosome 20p11.2 ...
Christopher Connolly   +3 more
wiley   +1 more source

A strategy to identify biliary atresia efficiently: A perspective from a Texas center. [PDF]

open access: yesWorld J Pediatr Surg
Harpavat S   +5 more
europepmc   +1 more source

Unveiling a New Link: Cholesterol Deficiency in Smith–Lemli–Opitz and Niemann–Pick C as a Driver of Ciliopathies

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1179-1191, June 2026.
ABSTRACT The ciliopathies are a group of genetic disorders caused by defective function of either the primary cilia (a large number) or the motile cilia (a much smaller number). These have been defined as diseases with mutations in genes encoding individual ciliary or cilia‐associated proteins.
Robert P. Erickson   +1 more
wiley   +1 more source

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