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Research 91–120 of 158
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- A Case of Onycholemmal Carcinoma in a 77-Year-Old Man
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Sterile matrix grafting for onycholysis in the setting of valproic acid use
- Alopecia areata: medical treatments
- Postural orthostatic tachycardia syndrome: a dermatologic perspective and successful treatment with losartan.
- Cronkhite-Canada Syndrome Associated With Superficial Esophageal Carcinoma: A Case Report and Literature Review
- Cutaneous manifestations of endocrine diseases in children
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Management of Alopecia and Onychomycosis in a Lupus Patient
- S2608 A Rare Case of Iron Deficiency Anemia: Cronkhite-Canada Syndrome
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Hair Loss and Polyposis in Cronkhite-Canada Syndrome
- Three Cases of Canine Dermatomyositis-Like Disease
- The study of consistent properties of gelatinous shampoo with minoxidil
- The Case Files
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Comparative Anatomy of Mouse and Human Nail Units
- Clinical and demographic characteristics associated with nail involvement in alopecia areata: A cross‐sectional study of 197 patients
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report