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Research 91–120 of 1000+
- Analogs of human genetic skin disease in domesticated animals
- Bachmann–Bupp syndrome and treatment
- Keratins and disease at a glance
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Hair loss
- Hair loss and its management in children
- Contents
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Diseases of Periocular Hair
- Hair loss in children.
- Dermatoscopy of hair shaft disorders
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Madarosis
- Disorders of the skin appendages
- Dermoscopy Research—An Update
- Adverse events associated with vismodegib: insights from a real-world pharmacovigilance study using the FAERS database
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- 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
- Conference 2022, The Sequel
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Diagnosis and management of hair loss in children
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Oral Manifestations of Hematologic and Nutritional Diseases
- Male fertility and skin diseases
- Diagnosis and Management of Alopecia in Children
- Cicatricial (Scarring) Alopecias
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Morpho-Regulation of Ectodermal Organs