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Research 301–330 of 1000+
- Congenital Lipedematous Alopecia in a 6-Year-Old Asian Boy
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Adverse Reactions to Oral Retinoids An Update
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Alternative uses of dermoscopy in daily clinical practice: An update
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- What does acne genetics teach us about disease pathogenesis?
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Dermatologic manifestations of endocrine disorders
- Congenital atrichia with papular lesions
- British Hair and Nail Society
- Adrenal causes of endocrine hypertension in childhood or adolescence
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Hair Loss in Children
- Genetic Defects of Female Sexual Differentiation
- American Academy of Veterinary Dermatology and American College of Veterinary Dermatology Annual Meeting, Norfolk, Virginia 4-8 April 2001
- Cutaneous manifestations of systemic infection in children
- Le gène<i>hairless</i>de la souris
- Keratin disorders: from gene to therapy
- The Hirsute Woman: Challenges in Evaluation and Management
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- Investigating tralokinumab-related adverse events in treating atopic dermatitis: insights from the FAERS database
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- 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
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings