Results 21 to 30 of about 4,952 (186)
Dupilumab for Trichothiodystrophy-Case Report and Review of the Literature. [PDF]
Clin Case RepABSTRACT Trichothiodystrophy (TTD) arises from pathogenic changes in several genes, most of which participate in DNA repair or transcriptional and translational processes. Atopic dermatitis may accompany TTD in a minority of cases. Dupilumab can offer a safe and effective treatment option for severe atopic dermatitis in this population.
O'Mahony J, O'Connor C.
europepmc +2 more sources
Early Skin Biopsy in Conradi-Hünermann-Happle Syndrome (X-Linked Dominant Chondrodysplasia Punctata). [PDF]
J Cutan PatholJournal of Cutaneous Pathology, Volume 52, Issue 10, Page 597-600, October 2025.
O'Connor C +4 more
europepmc +2 more sources
Lamellar ichthyosis in a female neonate without a collodion membrane [PDF]
, 2018 The term, autosomal recessive congenital ichthyosis (ARCI), describes a group of rare genetic skin diseases of cornification involving hyperkeratotic scaling at birth.
Aleshin, Maria +4 more
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CHARACTERISTICS OF COLLODION MEMBRANES FOR ULTRAFILTRATION [PDF]
Journal of General Physiology, 1953 An apparatus for the production of graded collodion membranes is described. The theoretical considerations of calibration are discussed in relation to the demonstrable structure and statistical characteristics of the membranes. A new definition of an "end-point" is suggested.
openaire +2 more sources
Artificial Cells, Nanomedicine, and Biotechnology, 2022 This review concentrates on how artificial cells can contribute to helping patients with COVID-19. Artificial cells have led to mRNA vaccines with more improvements to come.
Thomas Ming Swi Chang
doaj +1 more source
Collodion baby treated at a tertiary hospital in Tanzania: a case report
Journal of Medical Case Reports, 2018 Background The term “collodion baby” is used to describe a newborn covered with a translucent, parchment-like skin sheet. It is an extremely rare condition with an estimated incidence of 1 in 300,000 live births.
Evance K. Godfrey +3 more
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Clinical Case Reports, 2022 We report a unique case of self‐healing collodion baby (CB) that was successfully managed despite the risk of potentially serious complications. Self‐healing CB is a rare and distinct outcome of collodion phenotype occurring in approximately 10% of the ...
Nikolina Zdraveska +4 more
doaj +1 more source
Journal of Biochemical and Clinical Genetics, 2022 Background: The "autosomal recessive congenital ichthyosis (ARCI)" refers to a group of rare, heterogeneous, and non-syndromic disorders of keratinization, represented as abnormal scales over the entire body and attributable to defective ...
Gulhan Gurel, Muhsin Elmas, Basak Gogus
doaj +1 more source
THE SIZE OF PORES IN COLLODION MEMBRANES [PDF]
Journal of General Physiology, 1926 By the application of Poiseuille's law to the rate of flow of water through collodion membranes, it is calculated that the membranes used had pore radii of the order of 0.3 to 2 x 10–6 cm. On the same basis the number of pores per sq. cm. appears to vary from 270 x 1010 to 7 x 1010, decreasing with increase in pore size.
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Dupilumab Reduces Pruritus in Twins With Sjögren-Larsson Syndrome. [PDF]
Pediatr DermatolABSTRACT Sjögren–Larsson Syndrome (SLS), now termed ALDH3A2‐syndromic epidermal differentiation disorder (sEDD), is a rare genetic disorder marked by thickened skin, spasticity, and intellectual disability. Intractable pruritus is a nearly universal and debilitating feature of SLS that remains poorly managed by current therapies. We describe 4‐year‐old
Gallagher K +3 more
europepmc +2 more sources