Results 111 to 120 of about 14,871 (251)

Characterization of functional single jersey knitted fabrics using non-conventional yarns for sportswear [PDF]

open access: yes, 2018
Eight functional single jersey plain knitted fabrics have been developed in order to assess a quantitative analysis of various comfort-related properties in terms of thermal control, air and water vapor permeability, wickability, coefficient of kinetic
Fangueiro, Raúl   +5 more
core   +2 more sources

Corneal dystrophies

open access: yesOrphanet Journal of Rare Diseases, 2009
The term corneal dystrophy embraces a heterogenous group of bilateral genetically determined non-inflammatory corneal diseases that are restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value. Clinically,
Klintworth Gordon K
doaj   +1 more source

Sclerodermatomyositis [PDF]

open access: yes, 2011
The classification of rheumatic diseases is still challenging due to several reasons. First, those diseases have several differential clinical features, which giving overlap symptoms.
D, H. P. (H)   +4 more
core  

Immune status of patients with acne and concomitant skin malasseziosis

open access: yesPatologìâ, 2013
Introduction: Acne is the most common skin disease that affects up to 85% of people between 12 and 25 years old and 11% of persons over the age of 25 years.
E. Yu. Koretskaya
doaj   +1 more source

Subkutane Dirofilariasis: Infektion mit Dirofilaria repens. [PDF]

open access: yes, 1990
A female patient resident in Germany is described, who had developed dirofilariasis presenting as a hard subcutaneous nodule at the glabella. Dirofilaria repens was isolated after surgical removal of the skin lesion.
Barutzki, D.   +3 more
core   +1 more source

Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2. [PDF]

open access: bronze, 1998
Mary Porteous   +4 more
openalex   +1 more source

Familial keratosis follicularis spinulosa decalvans associated with woolly hair [PDF]

open access: bronze, 2007
Francesco Lacarrubba   +4 more
openalex   +1 more source

Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking [PDF]

open access: yes, 2018
Site-1 protease (S1P), encoded by MBTPS1, is a serine protease in the Golgi. S1P regulates lipogenesis, endoplasmic reticulum (ER) function, and lysosome biogenesis in mice and in cultured cells.
et al,, Kondo, Yuji, Patra, Debabrata
core   +1 more source

Whole genome linkage scan of recurrent depressive disorder from the depression network study [PDF]

open access: yes, 2017
Genome-wide linkage analysis was carried out in a sample of 497 sib pairs concordant for recurrent major depressive disorder (MDD). There was suggestive evidence for linkage on chromosome 1p36 where the LOD score for female-female pairs exceeded 3 (but ...
Boyd, Peter R.   +19 more
core  

Combined Abrocitinib and Acitretin Therapy for Darier’s Disease: A Case Report

open access: yesClinical, Cosmetic and Investigational Dermatology
Hui Ye,1,2,* Weifeng Chen,1,2,* Wenyan Liu,1,2 Junhui Zhu,1,2 Jingyao Liang,1,2 Xibao Zhang1,2 1Institute of Dermatology, Guangzhou Medical University, Guangzhou, Guangdong, 510095, People’s Republic of China; 2Department of Dermatology ...
Ye H   +5 more
doaj  

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