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Research 151–180 of 1000+
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Connexin mutations in human disease
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Analogs of human genetic skin disease in domesticated animals
- Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia
- Understanding skin morphogenesis across developmental, regenerative and evolutionary levels
- Alopecia in Cronkhite-Canada syndrome
- Dysfunction of keratinocyte adhesion
- Anatomy and Biology of Hair at Different Ages
- The Roles of EDA2R in Ageing and Disease
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- The amazing miniorgan: Hair follicle
- Integumentary System
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Approach to Alopecia in Dogs in Clinical Practice
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Polarized microscopy in genetic hair disorders: case series
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Congenital Atrichia: A Case Report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Molecular Basis of Hereditary Hair Diseases