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Research 31–60 of 1000+
- Congenital hypotrichosis due to short anagen
- Congenital hair loss disorders: Rare, but not too rare
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Congenital Triangular Alopecia (Brauer Nevus)
- An overview on congenital alopecia in domestic animals
- Congenital alopecia areata
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- 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.
- Congenital adrenal hyperplasia
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Eyelash trichomegaly: review of congenital, acquired, and drug‐associated etiologies for elongation of the eyelashes
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Ocular involvement caused by the accumulation of porphyrins in a patient with congenital erythropoietic porphyria
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Congenital adrenal hyperplasia
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Congenital Copper Deficiency: Copper Therapy and Dopamine‐β‐Hydroxylase Activity in the Mottled (Brindled) Mouse
- Molecular basis of congenital atrichia in humans and mice.
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- 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
- 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