Results 101 to 110 of about 4,952 (186)

Harlequin ichthyosis in a newborn: a rare and severe congenital ichthyosis. [PDF]

Pan Afr Med J
Tamgadge A, Gomase K.
europepmc   +1 more source

Severe staphylococcal scalded skin syndrome. [PDF]

IDCases
Nakyeyune ML, Bongomin F.
europepmc   +1 more source

A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris. [PDF]

Clin Case Rep, 2023
Shearer Z, White G, Steed JZ, Brown C, Venable T, Baber M.   +5 more
europepmc   +1 more source

Identification of Pathogenic Variants in <i>CYP4F22</i>, <i>FLG</i>, <i>ALOX12B</i>, and <i>NIPAL4</i> in a Case Series of Inherited Ichthyosis. [PDF]

Int J Mol Sci
Sattar MA, Zaib AA, Abbasi H, Abideen MZU, Riazuddin S, Ahmed ZM, Naeem M.   +6 more
europepmc   +1 more source

Novel Compound Heterozygous Mutations of TGM1 Gene Identified in a Turkish Collodion Baby Diagnosed with Non-Bullous Congenital Ichthyosiform Erythroderma. [PDF]

Ann Dermatol, 2023
Gülnerman EK, Hanedan N, Akillioglu M, Kayhan G, Adişen E, Erdem Ö, Hirfanoğlu İM, Ergenekon E, Önal EE, Türkyilmaz C, Koç E.   +10 more
europepmc   +1 more source

On the permeability of urea and some non-electrolytic substances through cell membrane.

(1) We studied the permeability of erythrocytes (human, an, chicken and frog), collodion membrane_ and frog's urinary bladder, to urea and its associated substances, alcohols and glucose.
Miyake, Yosio
core  

Case report of self-improving collodion ichthyosis in the newborn. [PDF]

J Int Med Res, 2023
Zhu S, Jiang Y, Shen N, Yin H, Qiao J.
europepmc   +1 more source

COLLODION MEMBRANES OF HIGH PERMEABILITY

Journal of Biological Chemistry, 1923
J.M. Nelson, David Percy Morgan
openaire   +1 more source

Congenital Ichthyosiform Erythroderma Superimposed with Chronic Dermatophytosis: A Report of Three Siblings

, 2016
Congenital ichthyosiform erythroderma is an autosomal recessive ichthyosis characterized by severe scaling and erythroderma. We report a family of three siblings who were all born with a collodion membrane and presented with diffuse scaling and pruritus.
Kannan, Swati, N Jahnke, Marla, Vyas, Nikki S, Choate, Keith A, Shwayder, Tor, Hu, Rong-Hua   +5 more
core  

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad. [PDF]

Medicine (Baltimore)
Al-Bustanji R, AlRababah BK, Rumman MSA, Abukhaled Y, Al-Rabadi N, Younis HKB, Ghalyon G, Al-Tawalbeh S, Aloudat O, Alrashdan MMM, Yamin MT, Maaita M, Salah AKD, Satari A.   +13 more
europepmc   +1 more source