Results 231 to 240 of about 73,460 (305)
Rare Genetic Variants Underlying Primary Immunodeficiency: Clinical, Pulmonary, and Genetic Insights from Two Pediatric Cases. [PDF]
Sikhayeva N +11 more
europepmc +1 more source
Classical complement activation in light and heavy chain deposition disease with acquired cutis laxa and bronchiolitis obliterans: a case report of monoclonal gammopathy of clinical significance. [PDF]
Chen Y +14 more
europepmc +1 more source
Abnormal von Willebrand factor multimer pattern without <i>VWF</i> variants in autosomal-recessive cutis laxa type IIA. [PDF]
Jacobs JW +5 more
europepmc +1 more source
Sodium thiosulphate for recalcitrant dystrophic calcinosis cutis ‒ An effective but tricky treatment option. [PDF]
Aparício Martins A, Pinho A.
europepmc +1 more source

