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- Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Congenital hair loss disorders: Rare, but not too rare
- Hirsutism causes and treatments.
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Pathogenesis and causes of hirsutism
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Evaluation of Premature Pubarche Cases: A Single CenterExperience
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Hair loss and its Unani concept and management
- Hair loss: An epidemiologic approach
- Clinical interest of a nonchemical lotion in head lice management
- The hair in childhood and old age
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Eyelash trichomegaly: review of congenital, acquired, and drug‐associated etiologies for elongation of the eyelashes
- Congenital alopecia areata: a systematic review
- Congenital alopecia areata
- A Hairy Paradox: Congenital Triangular Alopecia with a Central Hair Tuft
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Hereditary, Congenital, and Acquired Alopecias
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia