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Research 31–60 of 1000+
- Oral Manifestations of Hematologic and Nutritional Diseases
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Inherited Disorders of the Hair
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Congenital atrichia and hypotrichosis
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Morpho-Regulation of Ectodermal Organs
- 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
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Roles for Msx and Dlx homeoproteins in vertebrate development
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- The Basic Science of Hair Biology
- Current treatment of BPH
- Cutaneous Side Effects of Chemotherapy and Radiotherapy
- Hair Loss in Children
- Disorders of hair in children
- Dermatologic manifestations of COVID‐19: a comprehensive systematic review
- Genetic Defects of Female Sexual Differentiation
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Genetics of Human Skin Disease
- Hair and Nail Relationship
- PREVALENCE OF PERIODONTAL DISEASE IN WOMEN WITH POLYCYSTIC OVARY SYNDROME- A COMPARATIVE DESCRIPTIVE STUDY