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Research 151–180 of 1000+
- Progressively intractable seizures, focal alopecia, and hemimegalencephaly
- Finasteride use during pregnancy and early neonatal outcome: a case report
- Salivary Gland Choristoma (Heterotopic Salivary Gland Tissue) on the Anterior Chest Wall of a Newborn
- Reversible hypopigmentation of hair secondary to Vitamin B12 deficiency
- Netherton Syndrome
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Fetal Arrhythmia with a Myriad of Complications
- Mirror-image alopecia areata in mirror-image twins
- Spontaneous Lesions of Endangered Geriatric Julia Creek Dunnarts (<em>Sminthopsis douglasi</em>, Archer 1979) with Emphasis in Reproductive Pathology
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Alopecia totalis in an infant
- From Past to Present
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors
- Male pseudohermaphroditism due to 17β-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
- Pharmacology of antiandrogens
- Adverse Reactions to Oral Retinoids An Update
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Steroid 17β-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism
- Prenatal serological diagnosis of intrauterine cytomegalovirus infection.
- Congenital alopecia areata
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Alopecia in Rhesus macaques correlates with immunophenotypic alterations in dermal inflammatory infiltrates consistent with hypersensitivity etiology
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Analysis of Hair Cortisol as an Indicator of Chronic Stress in Pigs in Two Different Farrowing Systems
- Leishmaniasis in a dog native to Colorado
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Androgen levels and apoptosis in the testis during postnatal development of finasteride-treated male rat offspring
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Association of Infant Physical Development and Rapid Growth With Pubertal Onset Among Girls in Rural China