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Research 121–150 of 1000+
- A Hairy Paradox: Congenital Triangular Alopecia with a Central Hair Tuft
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Congenital Adrenal Hyperplasia
- Two different techniques for frontalis suspension using Gore-Tex to treat severe congenital ptosis
- Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia
- Giant pigmented tumour of the scalp—a diffuse neurofibroma or a congenital naevus showing neurofibromatous changes? Immunohistochemical and electron microscopic studies
- Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Congenital atrichia and hypotrichosis
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- Steroid 17-Hydroxyprogesterone in Hair Is a Potential Long-Term Biomarker of Androgen Control in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
- Recent advances in congenital ichthyoses
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- Scalp hair 17‐hydroxyprogesterone and androstenedione as a long‐term therapy monitoring tool in congenital adrenal hyperplasia
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Congenital atrichia with papular lesions
- 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
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Ectopic Adrenal Rests in Congenital Adrenal Hyperplasia as a Cause of Androgen Excess after Adrenalectomy Detected by Pelvic Venous Sampling
- Absence of Prostatic Growth in Large Cohort of Adult Female Patients with Congenital Adrenal Hyperplasia
- Management Approaches to Congenital Adrenal Hyperplasia in Adolescents and Adults; Latest Therapeutic Developments
- Early Diffuse Alopecia in a Neonate with Congenital Syphilis
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Resolution of pseudoainhum with acitretin therapy in a patient with palmoplantar keratoderma and congenital alopecia
- Generalized Congenital Hypotrichosis in a Female Rottweiler