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Research 31–60 of 79
- Cutaneous Tumours of Pilar Origin with Associated Syndromes
- Becker's Nevus with Ipsilateral Breast Hypoplasia: Improvement with Spironolactone
- Alopecia.
- Skin signs of systemic diseases
- Síndrome do nevo de Becker
- Primary scalp alopecia: new histopathological tools, new concepts and a practical guide to diagnosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Expression Patterns of Gli-1, Pleckstrin Homology-Like Domain, Family A, Member 1, Transforming Growth Factor-β1/β2, and p63 in Sebaceous and Follicular Tumors
- Alopecia areata incognita in Cronkhite-Canada syndrome
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Cronkhite-Canada Syndrome: A Case Report
- Congenital Combined Melanocytic Nevus of the Scalp With Associated Alopecia Areata
- Lifting the biofilm lid on the antibacterial and antibiofilm effects of sodium hypochlorite against <i>Staphylococcus aureus</i> in atopic dermatitis
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Nevus lipomatosus cutaneous superficialis with perifollicular fibrosis.
- Steatocystoma Multiplex
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Nevus Lipomatosus Superficialis With Dilated Hair Follicles
- Cutaneous Adnexal Cysts Revisited: What We Know and What We Think We Know
- Differentiation of the basal cell epithelioma-like changes overlying dermatofibroma.
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Panfolliculoma: report of two cases
- “Solitary fibrofolliculoma of the eyelid
- Trichofolliculoma With Mucinosis
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Folliculin: A surprising molecular brake in the human hair follicle
- Primary High‐Grade Ovarian Sertoli–Leydig Cell Tumor With Bilateral Adnexal Involvement in a Patient Diagnosed With Peutz–Jeghers Syndrome
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy