Results 101 to 110 of about 5,474 (244)

Regulating Access to Adult Content (with Privacy Preservation) [PDF]

open access: yes, 2015
In the physical world we have well-established mechanisms for keeping children out of adult-only areas. In the virtual world this is generally replaced by self declaration.
Finkelhor D.   +13 more
core   +1 more source

Differences in the morphological structure of the human tongue

open access: yesFolia Morphologica
BACKGROUND: The tongue exhibits significant individual variability in terms of shape, colour, and surface texture. Due to its location, it is easily accessible for medical examination, although often overlooked.
Klaudia Kulig   +3 more
doaj   +1 more source

The European contribution to osseous resective surgery for the treatment of residual pockets and furcation defects

open access: yesPeriodontology 2000, EarlyView.
Abstract For decades, osseous resective surgery along with apically positioned flap procedure has been advocated as a predictable treatment option to reduce residual pockets and minimize periodontal complications during supportive periodontal care. More recently, Fiber Retention Osseous Resective Surgery (FibReORS) has been suggested to reduce the ...
Gianfranco Carnevale   +3 more
wiley   +1 more source

Psoriasis is associated with fissured tongue but not geographic tongue: a prospective, cross‐sectional, case‐control study

open access: hybrid, 2021
Babak Itzinger-Monshi   +8 more
openalex   +1 more source

Intestinal Involvement in Kawasaki Disease [PDF]

open access: yes, 2018
To describe a case of Kawasaki disease with intestinal involvement and to analyze other published reports to define clinical characteristics, diagnostic issues, and therapeutic approaches of gastrointestinal involvement in Kawasaki ...
Cascio, Antonio   +9 more
core   +1 more source

ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis

open access: yesVeterinary Dermatology, EarlyView.
ABSTRACT Background Ichthyosis fetalis (IF), also known as harlequin ichthyosis, is a rare and often fatal autosomal recessive congenital skin disorder. It is characterized by thickened, hard skin plaques and deep skin fissures that limit mobility and cause malformations of the eyes, lips and ears.
Jeanna M. Blake   +2 more
wiley   +1 more source

The Case of a 28‐Year‐Old Woman With Medically Refractory Focal Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, Volume 13, Issue 2, Page 418-423, February 2026.
ABSTRACT We present the case of a 28‐year‐old right‐handed woman with medically refractory focal epilepsy. Her seizure semiology and electroencephalography (EEG) indicated a seizure onset zone in the right central‐parietal area. However, both MRI and PET scans were unremarkable, showing no focal lesions or areas of altered metabolism.
Rishi Sharma   +5 more
wiley   +1 more source

Extensive Intracerebral Hemorrhage Involving Basal Ganglia and Frontal Lobe With Intraventricular and Subarachnoid Extension in a Triplet Pregnancy Following In Vitro Fertilization: A Case Report and Review

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Triplet births, particularly those achieved by assisted reproductive technologies, entail markedly elevated maternal and fetal risks, including hypertensive diseases. Intracerebral hemorrhage is an uncommon but devastating complication during the postpartum period.
Raman Goit   +8 more
wiley   +1 more source

Oral mucosa alterations in a socioeconomically deprived region: prevalence and associated factors

open access: yesBrazilian Oral Research, 2011
This study aimed to evaluate the prevalence and factors associated with oral mucosa alterations in patients from Vale do Jequiti-nhonha, Brazil. The sample consisted of 511 patients of both genders.
Raquel Gonçalves Vieira-Andrade   +5 more
doaj   +1 more source

Identification of Novel Mutation in the ABCA12 Gene Causing Harlequin Ichthyosis

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Harlequin ichthyosis (HI) is an uncommon and extremely severe hereditary condition that primarily affects the skin. Infants born with this disorder display dense skin and prominent diamond‐shaped plates that cover a significant portion of their bodies.
Nadia Soltani   +5 more
wiley   +1 more source

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