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Research 30 of 965
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Alopecia in Cronkhite-Canada syndrome
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Cronkhite-Canada syndrome: A case report and literature review
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Alopecia areata incognita in Cronkhite-Canada syndrome
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Lifting the biofilm lid on the antibacterial and antibiofilm effects of sodium hypochlorite against <i>Staphylococcus aureus</i> in atopic dermatitis
- Cronkhite-Canada Syndrome: A Case Report
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Cronkhite–Canada syndrome: from clinical features to treatment
- TONGUE, RED
- Cases Report the Cronkhite-Canada Syndrome
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Review of systemic methotrexate therapy in pediatric dermatoses
- 463 Comorbid conditions associated with alopecia areata: A systematic review and update
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- Juvenile versus maturity-onset alopecia areata- a comparative retrospective clinical study
- Alopecia Areata: Prognostic Factors
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- 81 Juvenile RHUPUS syndrome: a case reports
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Cirmcumscribed juvenile pityriasis rubra pilaris in a 5-year-old-girl treated with topical keratolytic and steroid
- Clinical Profile of Methotrexate-resistant Juvenile Localised Scleroderma
- Heterogeneity of Polymorphous Light Eruption: A Study of 105 Patients
- Trachyonychia with juvenile pityriasis rubra pilaris