about
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinMutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeThe Humanistic, Societal, and Pharmaco-economic Burden of Angioedema.A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine.Socioeconomic burden of hereditary angioedema: results from the hereditary angioedema burden of illness study in Europe.HAE international home therapy consensus document.Presence of C1-inhibitor polymers in a subset of patients suffering from hereditary angioedemaProton pump inhibitor-induced subacute cutaneous lupus erythematosusAntiviral treatment of a boy with EBV-associated hydroa vacciniforme.Successful treatment of recalcitrant folliculitis barbae and pseudofolliculitis barbae with photodynamic therapy.[Facial angiofibromas associated to tuberous sclerosis treated with topical sirolimus].Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function.Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutationThe first Danish family reported with an AQP5 mutation presenting diffuse non-epidermolytic palmoplantar keratoderma of Bothnian type, hyperhidrosis and frequent Corynebacterium infections: a case report.Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary AngioedemaUnmasking sarcoidosis following surgery for Cushing disease.Acute dystonia mimicking angioedema of the tongue: a video-illustrated case.Estimation of EuroQol 5-Dimensions health status utility values in hereditary angioedema.ACE-inhibitor induced angio-oedema treated with complement C1-inhibitor concentrate.Use of a C1 Inhibitor Concentrate in Adults ≥65 Years of Age with Hereditary Angioedema: Findings from the International Berinert® (C1-INH) Registry.Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.Assessment of 105 Patients with Angiotensin Converting Enzyme-Inhibitor Induced Angioedema.Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema.Congenital self-healing reticulohistiocytosis - an important diagnostic challenge.Angioedema--assessment and treatment.Angiotensin-converting enzyme inhibitor-induced angioedema--a dangerous new epidemic.How Not to Be Misled by Disorders Mimicking Angioedema: A Review of Pseudoangioedema.Complement factor C4 activation in patients with hereditary angioedema.Drug-induced cutaneous lupus erythematosus: 88 new cases.Specific skin signs as a cutaneous marker of diabetes mellitus and the prediabetic state - a systematic review.Burden of Illness in Hereditary Angioedema: A Conceptual Model.Newborn with severe epidermolysis bullosa: to treat or not to treat?Life-threatening ACE inhibitor-induced angio-oedema successfully treated with icatibant: a bradykinin receptor antagonist.Hereditary angioedema: children should be considered for training in self-administration.Open-label, multicenter study of self-administered icatibant for attacks of hereditary angioedema.The humanistic burden of hereditary angioedema: results from the Burden of Illness Study in Europe.Henoch-Schönlein Purpura: A Literature Review.Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.The Use of Plasma-Derived Complement C1-Esterase Inhibitor Concentrate (Berinert®) in the Treatment of Angiotensin Converting Enzyme-Inhibitor Related Angioedema.Neurofibromatosis type 1 diagnosed in a child based on multiple juvenile xanthogranulomas and juvenile myelomonocytic leukemia.
P50
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