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- Molecular Basis of Hereditary Hair Diseases
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Skin diseases in the alpaca (<i>Vicugna pacos</i>): a literature review and retrospective analysis of 68 cases (Cornell University 1997–2006)
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Diseases of the skin. Treatment of scalp disorders.
- Zebrafish Model of Hereditary Pigmentary Disorders
- Hereditary, Congenital, and Acquired Alopecias
- Hereditary, Congenital, and Acquired Alopecias
- Hereditary, Congenital, and Acquired Alopecias
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Analogs of human genetic skin disease in domesticated animals
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Hair science and technology
- Inherited Disorders of the Hair
- Various types of alopecia and options of the treatment
- Genetic Basis of Male Pattern Baldness
- Male pattern hair loss
- The human keratins: biology and pathology
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- hKAP1.6 and hKAP1.7, Two Novel Human High Sulfur Keratin-Associated Proteins are Expressed in the Hair Follicle Cortex
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Advances in the treatment of androgenetic alopecia
- Relation between dermal papilla cells and androgenetic alopecia
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- ABC of Dermatology: Diseases of the hair and scalp
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets