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Research 30 of 39
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome.
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Male fertility and skin diseases
- Progeroide Syndrome
- Congenital atrichia and hypotrichosis
- Trichoscopy in Hair Shaft Disorders
- Werner′s syndrome
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Subject Index
- Diseases of Periocular Hair
- Premature graying of hair
- Hair loss in children.
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Role of the Wnt signaling pathway in keratoacanthoma
- Disorders of the skin appendages
- Description of skin lesions
- General Dermatology
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Madarosis
- Aging Skin: A Window to the Body
- Bhangra: Therapeutic and Pharmacological Actions in Shayb (Premature Greying of Hair)
- Hair loss in elderly women
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs