Results 141 to 150 of about 39,335 (209)

Identification of Candidate Surface Markers Associated With Osteogenic Potential in Human Dental Pulp‐Derived Cells

open access: yesOral Science International, Volume 24, Issue 1, January 2027.
ABSTRACT Aim Dental pulp‐derived cells have attracted attention as an accessible source of mesenchymal stem cell‐like cells for bone regeneration. However, donor‐to‐donor variability in osteogenic potential remains a challenge for their clinical application.
Makoto Watanabe   +11 more
wiley   +1 more source

How Allometry and Sexual Dimorphism Influence Cortical Bone Morphology at the Mandibular Symphysis in Modern Humans: A Comparative Study Using Elliptic Fourier Descriptors

open access: yesAmerican Journal of Biological Anthropology, Volume 191, Issue 3, November 2026.
ABSTRACT Objectives The modern human mandibular symphysis displays a mental prominence, a unique trait in the human lineage. Beyond this shared pattern, considerable variability in shape and metrics exists. This heterogeneity is thought to result from multiple mechanisms, including biomechanical compensation, allometric and dietary effects, population ...
Carla Degabriel   +4 more
wiley   +1 more source

Prenatal Diagnosis of Recurrent Fetal Intracranial Hemorrhage and a Maternally Inherited COL4A1 Variant of Uncertain Significance: A Case Report With Maternal Reverse Phenotyping

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT A 33‐year‐old woman with two consecutive pregnancies affected by fetal left periventricular germinal matrix hemorrhage (Grade IV) and progressive ventriculomegaly underwent trio whole‐exome sequencing. A heterozygous COL4A1 c.4249G>C (p.Gly1417Arg) variant, classified as a variant of uncertain significance, was identified in the fetus of the ...
Wei Shi   +9 more
wiley   +1 more source

Deep Intramuscular Vascular Malformations in Pediatric Klippel–Trenaunay Syndrome Mimicking Maffucci Syndrome: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Klippel‐Trenaunay syndrome (KTS) is a rare congenital vascular overgrowth disorder characterized by capillary and venous or lymphatic malformations with limb hypertrophy. Deep intramuscular involvement in children is uncommon and may resemble other vascular‐overgrowth syndromes.
Syeda Simrah Shah   +9 more
wiley   +1 more source

Placento-cerebral adhesion: a morphology-based classification derived from a case report and literature review. [PDF]

open access: yesChilds Nerv Syst
Kroczek K   +6 more
europepmc   +1 more source

Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 175, Issue 2, Page 877-884, November 2026.
Abstract Objective Vasculitis is an infrequent pathology among reproductive‐aged women. While data exists regarding pregnancy outcomes in the more common vasculitis subtypes, data is limited regarding these outcomes in rare vasculitis subtypes. We aimed to compare pregnancy and perinatal outcomes between women who suffered from rare types of vasculitis
Uri Amikam   +4 more
wiley   +1 more source

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