Results 81 to 90 of about 29,128 (218)

Evaluation of some chronical diseases in etiopathogenesis of demodicosis

open access: yesDermatologica Sinica, 2017
Background: The aim of this study is to assess the effect of chronic diseases on the etiopathogenesis of demodicosis through the determination of Demodex sp. positivity in the face and eyelashes of the people with the chronic disease. Methods: This study
Zeynep Tas Cengiz   +4 more
doaj   +1 more source

Micro scalar patterning for printing ultra fine solid lines in flexographic printing process [PDF]

open access: yes, 2018
This research focuses on the study of ultra-fine solid lines printing by using Micro-flexographic machine which is combination of flexography and micro-contact printing technique.
Hassan, Suhaimi
core   +1 more source

Premixed Lidocaine With Fospropofol Disodium for Safety and Clinical Evaluation Regarding Paresthesia Upon Fospropofol Disodium Injection: A Preclinical Experimental Study and a Randomized Controlled Trial

open access: yesMedComm, Volume 7, Issue 4, April 2026.
This study explored the effect of lidocaine premixing on fospropofol‐induced paresthesia. While the mixture of fospropofol (FP) and lidocaine (LD) proved chemically stable and safe in preclinical tests, clinical results from randomized controlled trial showed no reduction in paresthesia in FP+LD group compared with FP+NS group.
Bo Jiao   +17 more
wiley   +1 more source

Camel Anatomy; More Than Just a Hump [PDF]

open access: yes, 2019
The one-humped camel (Camelus dromedarius) is capable of living in extreme, arid environments due to its numerous anatomical adaptations. Its modified features of the muscular system, integument, skeletal system, and several internal organs allow this ...
Chase, Michael
core   +1 more source

Hypothyroidism, eyelash loss [PDF]

open access: yesCleveland Clinic Journal of Medicine, 2020
Hiroki, Matsuura, Yu, Suganami
openaire   +2 more sources

Managing Skin Side Effects Associated With Oncology Treatments: Asian Perspective on Use of Dermocosmetics

open access: yesAsia-Pacific Journal of Clinical Oncology, Volume 22, Issue 2, Page 186-198, April 2026.
Skin adverse events (AEs) frequently accompany all types of anticancer treatments. This publication discusses how recent international guidance on best‐practices use of dermocosmetics can be adapted to the North Asia region (China, Hong Kong, Japan, Republic of Korea, and Taiwan).
Meng Pan   +9 more
wiley   +1 more source

Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center

open access: yesClinical Genetics, Volume 109, Issue 4, Page 707-716, April 2026.
Chromatinopathies (CP) are a growing group of rare genetic disorders characterized by cognitive deficits and growth abnormalities. This is the largest collection of CP to date, contributing to a deeper understanding of the landscape and diagnosis of these rare diseases, strongly improved by the use of large‐scale sequencing technologies.
Giulia Bruna Marchetti   +16 more
wiley   +1 more source

PECULIARITIES OF REACTION TO THE EYELASHES INTRUSION INTO THE EYE IN CASE OF PENETRATING OCULAR INJURY

open access: yesОфтальмохирургия, 2015
Purpose. To show the variations of eye reaction to the eyelashes intrusion into the eye in case of the penetrating ocular injury.Materials and methods. We observed 5 patients with eyelashes intruded into the eye during the penetrating ocular injury using
T. A. Krasnovid   +3 more
doaj  

Comparison of oral prednisolone pulse therapy with intravenous methylprednisolone pulse therapy in severe alopecia areata [PDF]

open access: yes, 2013
Objective: To compare the efficacy of oral prednisolone pulse therapy in comparison to the intravenous methylprednisolone pulse therapy in treatment of severe alopecia areata. Patients and methods: In this interventional study, all patients with alopecia
Alborzi, A., Dehghan, A., Shahini, N.
core  

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

Home - About - Disclaimer - Privacy