Search
for
Sort by
Research 61–90 of 1000+
- Psychoactive drugs and skin
- Clinical review 74: Dermatological manifestations of endocrine disorders.
- Drug eruptions in dermatology
- Skin manifestations of endocrine diseases
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Neuroimaging of sleep and depression
- Cutaneous manifestations of systemic infection in children
- Adverse Cutaneous Reactions to Antidepressants
- Dermatologic manifestations of endocrine disorders
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Cutaneous reactions to chemotherapeutic drugs and targeted therapy for cancer
- Skin Conditions in Figure Skaters, Ice-Hockey Players and Speed Skaters
- Trichoscopy in Hair Shaft Disorders
- Scalp Itch: A Systematic Review
- Dermoscopy Update: Review of its Extradiagnostic and Expanding Indications and Future Prospects
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Guidelines for the Use of Acitretin in Psoriasis
- Hair Loss in Children
- Multiple Autoimmune Syndrome type 3- Thyroiditis, Vitiligo and Alopecia Areata
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Topical minoxidil for nail growth: A conventional medication with a novel indication
- Isolated Nail Lichen Planus in an Indian Boy
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome