Search
for
Sort by
Research 31–60 of 1000+
- A new type of pachyonychia congenita.
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Traumatic panniculitis with hypertrichosis
- Pathologies of the skin and its appendages in endocrine diseases
- Hirsutism
- [Wooly hair syndrome. Clinical and microscopic study].
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- News in brief
- Inherited Disorders of the Hair
- Disorders of hair in infants and children other than alopecia
- Disorders of the Hair and Nails
- Pathology in Practice
- Nutritional Skin Diseases
- Evaluation of the Safety and Effectiveness of Oral Minoxidil in Children: A Systematic Review
- Cetuximab-induced hypertrichosis of the scalp and eyelashes
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- PRIDE syndrome with lumbosacral hypertrichosis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Hypertrichosis of the pinnae in a patient using panitumumab
- Facial hypertrichosis after isotretinoin therapy: Is it a side effect or coincidence?
- Congenital atrichia and hypotrichosis
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Focal and Generalized Alopecia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Sarolaner, a novel parasiticide in the treatment of generalized demodicosis in dogs-a case study
- Coming full circle (almost): Low dose oral minoxidil for alopecia
- Diffuse face and ear hypertrichosis caused by 5% topical minoxidil in an adult woman with spontaneous resolution
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year