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Research 331–360 of 1000+
- The pharmacology of methotrexate
- Perspectives on Dermatopathology
- British Hair and Nail Society
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Common Baldness in Women
- Disorders of the skin appendages
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- National scientific medical meeting 1996 abstracts
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- A rare hair loss in children: Monilethrix
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- 157 Analysis of the hybrid schwannoma and neurofibroma including a case report of schwannomatosis caused by a mutation in the LZTR1 gene
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- TONGUE, RED
- Dysfunction of keratinocyte adhesion
- Steatocystoma Multiplex
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Exploring the Dermoscopic Patterns in Tuberous Sclerosis