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Research 241–270 of 1000+
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Keratosis follicularis spinulosa decalvans in a family
- Dental manifestations in Vitamin D dependent rickets Type II with Alopecia: a short pictorial case report
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- Defining compartmentalized stem cell populations with distinct cell division dynamics in the ocular surface epithelium
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- A Survey of Women Polycystic Ovarian Disease (PCOD)
- A Survey of Women Polycystic Ovarian Disease (PCOD)
- 011 Central Centrifugal Cicatricial Alopecia (CCCA) Under the Scope: Histological Similarities between CCCA and Lichen Planopilaris
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Alopecia and cardiovascular events
- Dermatopathology Update
- Vitiligo
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Polycystic Ovarian Syndrome in Female players
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Healthcare innovation and patent law’s ‘pharmaceutical privilege’: is there a pharmaceutical privilege? And if so, should we remove it?
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains