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Research 601–630 of 1000+
- 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
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Pseudo "fringe sign" in frontal fibrosing alopecia
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Pathogenesis of androgenetic alopecia
- Fever of unknown origin in a male patient with systemic lupus erythematosus.
- CENTRAL STATES DERMATOLOGICAL SOCIETY
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Hodgkin′s lymphoma presenting as alopecia
- Clinical Description of Frontal Fibrosing Alopecia with Concomitant Lichen Planopilaris
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Deciphering the Role of Androgen in the Dermatologic Manifestations of Polycystic Ovary Syndrome Patients: A State-of-the-Art Review
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Alopecia universalis after injection of messenger RNA COVID-19 vaccine. A case report
- Werner's syndrome: incidental finding during pregnancy
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Cause of Androgenic Alopecia
- Monilethrix in three generations
- A papular eruption on the face. A distinct subtype of lichen planopilaris?
- Lichen Planopilaris
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Risk factors for sebaceous gland diseases and their relationship to gastrointestinal dysfunction in Han adolescents