Results 91 to 100 of about 888 (167)
Cutaneous and mucosal manifestations associated with celiac disease [PDF]
, 2018 Beteta Gorriti, Valia Patricia +6 more
core +2 more sources
Hair Shaft Disorders in Children - An Update. [PDF]
Indian Dermatol Online J, 2023 Bhat YJ, Trumboo T, Krishan K.
europepmc +1 more source
Decompensation of Refsum Disease Caused by Ibuprofen Intake [PDF]
, 2009 Esber, Natacha, Schulz, Thomas
core +2 more sources
Significance of connexion genes in non-syndromic deafness in Africans [PDF]
, 2013 Includes abstract.
Bosch, Jason
core
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 1. [PDF]
J Mov Disord, 2021 Mukherjee D +5 more
europepmc +1 more source
The first reported case of trichothiodystrophy in Hungary: A young male patient with mutations in the ERCC2 gene [PDF]
, 2018 Trichothiodystrophy, also called sulphur-deficient brittle hair syndrome, is a rare autosomal recessive genetic disorder of DNA repair and transcription.
Béla Háromszéki +6 more
core +1 more source
Measuring the impact of pruritus in patients with epidermolysis bullosa: evaluation with an itch-specific instrument. [PDF]
Dermatol Reports, 2023 Alheggi A +6 more
europepmc +1 more source
Congenital icthyosis: A case report [PDF]
Clinical Research and Trials, 2017 openaire +1 more source