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Research 30 of 237
- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- Over-expression of thymosin beta4 promotes abnormal tooth development and stimulation of hair growth
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The eye and the skin in endocrine metabolic diseases
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Congenital atrichia and hypotrichosis
- Use of chemotherapy during human pregnancy
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Inherited Disorders of the Hair
- Treatment of acne vulgaris: a literature review / Lečenje običnih akni (acne vulgaris) – pregled literature
- BRIDGING THE GAP IN ACNE MANAGEMENT: A NARRATIVE REVIEW OF CURRENT THERAPIES AND THE EMERGENCE OF CLASCOTERONE
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Inherited Epidermolysis Bullosa: A Clinical Case
- Mucocutaneous Manifestations of Endocrine Disorders
- Disorders of hair in children
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Hairless is a nuclear receptor corepressor essential for skin function