Search
for
Sort by
Research 151–180 of 158
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Clouston’s syndrome: a rare case report
- Subject Index
- Subject Index
- Prophylaxis and Management of Skin Toxicities
- Cutaneous Side Effects of Modern Targeted Therapy and Immunotherapy in Patients with Dermatological Malignancies
- Alopecia Universalis, Onychodystrophy, and Total Vitiligo
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Onychodystrophy With Associated Polymicrobial Distal Phalanx Osteomyelitis
- 0447 Minoxidil for onychodystrophy: Can this hair loss remedy be a nail growth remedy?
- A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically
- Juvenile versus maturity-onset alopecia areata- a comparative retrospective clinical study
- Immune-related alopecia (areata and universalis) in cancer patients receiving immune checkpoint inhibitors
- Cutaneous Reactions to Chemotherapeutic Agents
- Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Case of Cronkhite Canada syndrome shows improvement with enteral supplements.
- Dermatological concerns for women and girls with turner syndrome
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Cronkhite-Canada Syndrome: an unusual finding of gastro-intestinal adenomatous polyps in a syndrome characterized by hamartomatous polyps
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Olmsted syndrome
- Nearly complete hair re-pigmentation in an older patient treated with hydroxyurea for essential thrombocytosis