Results 251 to 260 of about 31,665 (304)
Protocol for the Development of a Core Outcome Set for Inherited Ichthyosis.
DermatologyRossel V +8 more
europepmc +1 more source
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Nature Reviews Disease Primers, 2023
This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature's AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections.
, Masashi, Angela Hernandez-Martin
exaly +6 more sources
This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature's AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections.
, Masashi, Angela Hernandez-Martin
exaly +6 more sources
Inherited ichthyosis: Non‐syndromic forms
Journal of Dermatology, 2016Takuya Takeichi
exaly +2 more sources
JAMA Dermatology, 2023
This case report describes a patient in her 30s who was born with ichthyosis who presented with plate-like scale that covered her whole body as well as ectropion.
Yi-Cheng, Wu, Qiang, Yao
openaire +2 more sources
This case report describes a patient in her 30s who was born with ichthyosis who presented with plate-like scale that covered her whole body as well as ectropion.
Yi-Cheng, Wu, Qiang, Yao
openaire +2 more sources
Experimental Dermatology, 2021
Autosomal recessive congenital ichthyosis (ARCI) is a rare and heterogeneous skin cornification disorder presenting with generalized scaling and varying degrees of erythema.
J. Mohamad +24 more
semanticscholar +1 more source
Autosomal recessive congenital ichthyosis (ARCI) is a rare and heterogeneous skin cornification disorder presenting with generalized scaling and varying degrees of erythema.
J. Mohamad +24 more
semanticscholar +1 more source
British Journal of Dermatology, 1983
We describe four patients with congenital follicular hyperkeratosis, of whom three also had pseudoacanthosis nigricans and two had facial abnormalities. Skin specimens were studied by light microscopy, autoradiography, histochemistry and scanning electron microscopy, and the results were compared with those from patients with keratosis pilaris.
M, Hazell, R, Marks
openaire +2 more sources
We describe four patients with congenital follicular hyperkeratosis, of whom three also had pseudoacanthosis nigricans and two had facial abnormalities. Skin specimens were studied by light microscopy, autoradiography, histochemistry and scanning electron microscopy, and the results were compared with those from patients with keratosis pilaris.
M, Hazell, R, Marks
openaire +2 more sources