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Research 301–330 of 1000+
- An Update of Congenital Adrenal Hyperplasia
- Frontal fibrosing alopecia: a retrospective clinical review of 62 patients with treatment outcome and long-term follow-up
- Frontal Fibrosing Alopecia: A Retrospective Analysis of 72 Patients from a German Academic Center
- A cross-sectional study of male balding patterns in people of color
- Alopecia fibrosante frontal
- A study of the Geheimratsacken angle as predictor for early diagnosis of androgenetic alopecia in adolescent population
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- Total Hairline Correction in Female Patient
- Estrogen hormone therapy stabilizes lateral hairline in transfeminine patients: Implications for facial feminization surgery
- Acute telogen effluvium triad after resolution
- Excimer 308-nm laser for the treatment of frontal fibrosing alopecia: an observational study in 30 patients
- Inherited Epidermolysis Bullosa: A Clinical Case
- Atrichia With Papular Lesions
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Frontal Fibrosing Alopecia: Update and Review of Challenges and Successes
- Frontal Alopecia after Repeated Botulinum Toxin Type A Injections for Forehead Wrinkles: An Underestimated Entity?
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- A new strategy to modulate alopecia using a combination of two specific and unique ingredients.
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Evaluation of microneedling in the treatment of frontal fibrosing alopecia
- No-Shave Long Hair Follicular Unit Excision Using an All-Purpose Skin-Responsive Device
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- 원저 : 한국인에 있어 유전성안드로겐 탈모증의 유병율과 임상 유형
- Androgenetic Alopecia
- Netherton Syndrome Associated with Growth Hormone Deficiency
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11