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Research 151–180 of 158
- Integrative medicine - combination of conventional medicine and traditional herbal medicine may find its potential applications in the treatment of certain dermatological and endocrine diseases – review of the literature
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Summary on SHANG Hong-tao's Experience in Treating Alopecia of Spleen Deficiency with Shengyang Sanhuo Decoction (升阳散火汤)
- Toxic and Metabolic Disorders of the Nervous System
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Atractylodes macrocephala Koidz. Stimulates Dermal Papilla Cells to Promote Anagen Entry Associated with GSK3β/β-Catenin Signaling
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Unruly hair
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- TLRgeting Evasion of Immune Pathways in Glioblastoma
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Transcutaneous implantation of valproic acid-encapsulated dissolving microneedles induces hair regrowth
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Molecular pathology of skin adnexal tumours
- Dermatologic manifestations of endocrine disorders
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Differential plasma proteome analysis reveals key proteins associated with insulin resistance in acne vulgaris patients