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Research 751–780 of 1000+
- Erythematous Plaque on the Scalp With Alopecia
- Non infectious dermatoses of the scalp a north indian study
- The Pathogenesis of Primary Cicatricial Alopecias
- Folliculitis
- Short Anagen Syndrome
- Pili torti in association with citrullinemia
- The Friar Tuck sign in trichotillomania
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Latent polyglandular autoimmune syndrome type 2 case diagnosed during a shock manifestation
- Atlas of Geriatric Dermatology
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- Netherton Syndrome
- Phenotypic characterization of non-dermatophyte moulds from companion animals with mycotic dermatitis
- Corkscrew Hairs in Trichoscopy of Trichotillomania
- Dermatological alterations induced by gynecological hormonal imbalances: Acne, hirsutism and alopecia
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Lipedematous scalp with lipedematous alopecia: A case report
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- A Review on: The Herbal Approach to PCOD
- Clinical and Reproductive Profile of Women with Polycystic Ovarian Syndrome Attending the Department of Obstetrics and Gynecology: A Retrospective Hospital-Based Study
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Dermatoscopy: Alternative uses in daily clinical practice
- Alopecia Areata
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- National consensus on the management of patients with hyperandrogenism (2016)
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi