Results 161 to 170 of about 111,824 (315)

Changes in the Pterygopalatine and Midpalatal Sutures After Rapid Palatal Expansion With Tooth‐Bone‐Borne (MARPE) and Tooth‐Borne (Hyrax) Appliances

open access: yesOrthodontics &Craniofacial Research, EarlyView.
ABSTRACT Objective This retrospective cohort study aimed to compare the effects of tooth‐bone‐borne mini‐implant‐assisted rapid palatal expansion (MARPE) and tooth‐borne (Hyrax) rapid palatal expansion (RPE) techniques on the pterygopalatine suture (PPS) and the opening pattern of the midpalatal suture (MPS).
Maria Antônia Netto Barbosa   +3 more
wiley   +1 more source

Management of Azoospermia: A Systematic Approach

open access: yesThe Obstetrician &Gynaecologist, EarlyView.
ABSTRACT Key Content Work‐up of azoospermic men includes a detailed history, physical examination and investigations to find the underlying cause. Causes and management of azoospermia (pre‐testicular, testicular and post‐testicular) with case presentations.
Naimah Raza   +3 more
wiley   +1 more source

Choanal Atresia [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1947
openaire   +2 more sources

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

First Korean Case of 5q35.2q35.3 Microduplication With Reversed Sotos Syndrome Phenotype and Growth Hormone Deficiency: Expanding the Endocrine Spectrum

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1696-1701, July 2026.
ABSTRACT Sotos syndrome is an overgrowth disorder caused by nuclear receptor binding SET domain protein 1 (NSD1) haploinsufficiency, whereas reciprocal 5q35.2q35.3 microduplication produces a reversed phenotype with growth retardation, microcephaly, delayed bone age, and neurodevelopmental delay.
Sejin Kim, Jung Sook Ha, Jun Chul Byun
wiley   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

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