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Research 481–510 of 1000+
- Congenital localized basaloid follicular hamartoma: a case report and review of the literature
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- CONGENITAL ATRICHIA.*
- Congenital atrichia with papular lesions
- Congenital cutaneous lymphadenoma
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Congenital milia En plaque on scalp
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Congenital hypotrichosis in a French bulldog
- Congenital triangular alopecia
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Congenital triangular alopecia - A case report
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Congenital Combined Melanocytic Nevus of the Scalp With Associated Alopecia Areata
- Cutaneous Mastocytosis Associated With Congenital Alopecia
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from South Dakota
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- The distribution of Preputial vessels in different severity of rat congenital hypospadias model: imaging study using micro-computerized tomography
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Congenital atrichia associated with nevus flammeus: A rare association
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Congenital Lipedematous Alopecia in a 6-Year-Old Asian Boy
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- 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
- Giant Congenital Blue Nevus Presenting as Cutis Verticis Gyrata: A Case Report and Review of the Literature
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Familial congenital generalized hypertrichosis