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- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- 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
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Congenital atrichia and hypotrichosis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Inherited Disorders of the Hair
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Cutaneous manifestations of systemic infection in children
- 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
- 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
- Disorders of hair in children
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT