Results 111 to 120 of about 16,240 (205)

Severe staphylococcal scalded skin syndrome. [PDF]

IDCases
Nakyeyune ML, Bongomin F.
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

A case of self-healing collodion baby

Przegląd Dermatologiczny, 2021
Aleksandra Kitowska, Piotr Brzeziński, Justyna Słomka, Mieczysława Karcz, Józef Jasonek   +4 more
doaj   +1 more source

High molecular thyrotrophin ("big"-TSH) from human pituitaries : Preparation and partial characterization [PDF]

, 1977
Erhardt, F., Scriba, Peter Christian
core   +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

A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma [PDF]

, 2014
Barnicoat, A, Drury, S, Harper, JI, Khan, A, Kinsler, VA, Lench, N, O'Shaughnessy, RF, Rukaite, G, Waelchli, R   +8 more
core   +1 more source

Handling the Heavens : Things and the Photo-Objects of Astronomy

, 2020
Nasim, O.
core  

Beyond the skin: immunological profiles and infectious complications in ALOX12B-associated autosomal recessive congenital ichthyosis. [PDF]

Front Immunol
Sefer AP, Catak MC, An I, Keser Ozturk N, Baykal Selcuk L, Dincer OS, Benamar M, Getachew F, Schmitz-Abe K, Agrawal PB, Bayram Catak F, Erman B, Bilgic Eltan S, Karakoc Aydiner E, Ozen A, Chatila T, Baris S.   +16 more
europepmc   +1 more source

Congenital Ichthyosis - Collodion Baby Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Priyanka Srivastava, Anuj Srivastava, Prachi Srivastava, Anupama Vithal Kumar Betigeri, Minakshi Verma   +4 more
doaj   +1 more source

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