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Research 31–60 of 1000+
- Clouston syndrome associated with eccrine syringofibroadenoma
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- The fundamentals of WNT10A
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Genetics of Structural Hair Disorders
- Congenital atrichia and hypotrichosis
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- El teorema del 0,7 o el otro teorema de Pitágoras
- Trichoscopy in Hair Shaft Disorders
- Analogs of human genetic skin disease in domesticated animals
- Polarized microscopy in genetic hair disorders: case series
- <i>WNT10A</i> , dermatology and dentistry
- Molecular Basis of Hereditary Hair Diseases
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Dermatopathology and molecular genetics
- Inherited Disorders of the Hair
- Ugreelig hår
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Genetic Hair Disorders: A Review
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Index
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Current Genetics in Hair Diseases
- Biology and Genetics of Hair
- New-Onset Gastrointestinal Polyposis
- Skin Development and Disease: A Molecular Perspective
- Hair shaft structures in EDAR induced ectodermal dysplasia