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- Skin Manifestations in Primary Immunodeficient Children
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Melanocytes: The new Black
- Zebrafish Model of Hereditary Pigmentary Disorders
- Analogs of human genetic skin disease in domesticated animals
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Melanocytes and Vitiligo (and Hair Graying)
- Cutaneous signals of immune system disease
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Premature graying of hair
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Diseases of Periocular Hair
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Dissecting the boundary of quiescence and activation of murine melanocyte stem cells in the hair follicle niche
- A cross sectional study on geriatric dermatosis in patients attending a tertiary care hospital
- Description of skin lesions
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- Madarosis: A marker of many Maladies
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Pharmacotherapy for Keloids and Hypertrophic Scars
- Partial biotinidase deficiency: Clinical and biochemical features
- A Mutation of the Androgen Receptor Associated with Partial Androgen Resistance, Familial Gynecomastia, and Fertility*