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- Case Report: Loss of Pubic and Axillary Hair Following Treatment with Glucocorticoids
- Two females with hair loss
- A Unique Acquired Athletic Dermatologic Condition in a Half Marathon Participant: An Autobiographical Case Report of Sports-Associated Clothing Related Axillary Tangled Clumped Hairs (SCRATCH)
- Scalp Dermatology for the Hair Restoration Surgeon Trichotemnomania
- Liposuction with Diode Laser Ablation for Treatment of Axillary Osmidrosis
- Effects of Hormones and Endocrine Disorders on Hair Growth
- Pruritic axillary papules in a 14‐year‐old girl
- Immune-mediated Coombs negative intravascular haemolysis in systemic lupus erythematosus (SLE)
- Essential syphilitic alopecia revisited
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Psychosis as a late manifestation of Sheehan’s syndrome
- Frontal fibrosing alopecia after antiandrogen hormonal therapy in a male patient
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Stigmata of Liver Disease in a Cirrhotic Patient
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Hair Transplantation to the Axillae
- The secretory clear cell of the eccrine sweat gland as the probable source of excess sweat production in hyperhidrosis
- Fox-Fordyce Disease
- Diseases of the Hair
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Questions and Answers
- SAT-134 Postmenopausal Virilization: Rare Case of an Ovarian Tumor Not Easily Identified on Imaging
- A case report of Graham-Little–Piccardi–Lassueur syndrome
- Frontal fibrosing alopecia: a survey in 16 patients
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant
- Granulomatosis Disciformis Chronica et Progressiva With Lymphadenopathy
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Mucocutaneous manifestations of acquired hypoparathyroidism: An observational study
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient