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- Diffuse Alopecia in a Hemodialysis Patient Caused by a Low-Molecular-Weight Heparin, Tinzaparin
- Combined Molecular Hydrogen and Vitamin C Treatment in Irradiated Normal and Cancer Cell Models: An Exploratory In Vitro Study and Case Reports
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Equine Dermatophytosis caused by Nannizzia gypsea - Molecular Diagnosis by qPCR
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Deep facial mycosis due to <i>Trichophyton verrucosum</i>—molecular genetic identification of the dermatophyte in paraffin‐embedded tissue—case report and review of the literature
- Primary Cutaneous Rhabdoid Squamous Cell Carcinoma: A Case Report and Review of Molecular Features
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Enhancing diagnostic yield of monogenic diabetes through phenotypic and molecular reanalysis of 128 individuals with young onset hyperglycemia: highlighting the significance of accurate case characterization
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Case Report: Alopecia areata in an adolescent after COVID-19 infection
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature
- Hair extensions: a concerning cause of hair disorders
- Combing the genome for the root cause of baldness
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- The twisting tale of woolly hair: a trait with many causes
- Re-discovery of Trichophyton bullosum in North Africa as a cause of severe dermatophytosis in donkeys
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- ILDS Newsletter No. 29
- White piedra: molecular identification of Trichosporon inkin in members of the same family
- Genetic mapping of hair loss through the APCDD1 gene pathway: A new perspective
- Männlicher Haarausfall – was uns unsere Gene verraten
- Generalised cutaneous necrosis: a complication of low-molecular-weight heparin
- Molecular basis of androgen insensitivity
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy